Mcccd pipelineaz com

Business, Entrepreneurialism, and Management

Statement Clerks

Prepare and distribute bank statements to customers, answer inquiries, and reconcile discrepancies in records and accounts.

Salary Breakdown

Statement Clerks

Average

$39,590

ANNUAL

$19.03

HOURLY

Entry Level

$30,260

ANNUAL

$14.55

HOURLY

Mid Level

$40,870

ANNUAL

$19.65

HOURLY

Expert Level

$51,480

ANNUAL

$24.75

HOURLY


Current Available

Statement Clerks

894

Current Available Jobs


Top Expected Tasks

Statement Clerks


Knowledge, Skills & Abilities

Statement Clerks

Common knowledge, skills & abilities needed to get a foot in the door.

KNOWLEDGE

Customer and Personal Service

KNOWLEDGE

Clerical

KNOWLEDGE

English Language

KNOWLEDGE

Computers and Electronics

KNOWLEDGE

Economics and Accounting

SKILL

Reading Comprehension

SKILL

Active Listening

SKILL

Speaking

SKILL

Critical Thinking

SKILL

Service Orientation

ABILITY

Near Vision

ABILITY

Oral Comprehension

ABILITY

Problem Sensitivity

ABILITY

Oral Expression

ABILITY

Deductive Reasoning


Job Opportunities

Statement Clerks

  • Office Clerk
    Kelly Services    Phoenix, AZ 85067
     Posted about 1 hour    

    **At Kelly** **®** **Professional & Industrial, we’re passionate about helping you find a job that works for you. How about this one?** We’re seeking an Office Clerk to work at to work at a top-tier client in Phoenix, AZ. With us, it’s all about finding the job that’s just right.

    **Position Title:** Office Clerk

    **Location:** Phoenix, AZ 85009

    **Pay Rate:** $18.00

    **Shift:** M-F: 7:30am – 4:30pm

    **Duration:** through 1/2023

    **Job Description**

    Office clerk is responsible for the organization and coordination of office operations and procedure.

    **Responsibilities:**

    • Received telephone calls, screening those can be handled without supervisor’s assistance.

    • Perform administrative support tasks. Such as assisting with pay records, invoices, balance sheets or other documents.

    • Participates in training, follows safety procedures, job duties and company policies.

    • Any other duties as assigned.

    **Requirements**

    • Associate's degree or comparable experience

    • Excellent Communication

    • Experience with Microsoft office (Outlook, Excel, & Word)

    • Organization Skills, Attention to Detail

    Steel toe boots

    **What happens next**

    Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. That means all our recruiters will have access to your profile, expanding your opportunities even more.

    Helping you discover what’s next in your career is what we’re all about, so let’s get to work. Apply to be an Office Clerk today!

    **Get a complete career fit with Kelly** **®** **.**

    You’re looking to keep your career moving onward and upward, and we’re here to help you do just that. Our staffing experts connect you with top companies for opportunities where you can learn, grow, and thrive. Jobs that fit your skills and experience, and most importantly, fit right on your path of where you want to go in your career.

    **About Kelly** **®**

    At Kelly, we’re always thinking about what’s next and advising job seekers on new ways of working to reach their full potential. In fact, we’re a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live (plus, did we mention we provide a ton of benefits ?). Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.

    Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly’s Human Resource Knowledge Center.
    Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.


    Employment Type

    Full Time

  • Clinical Research Associate - Home-Based (Southern California)
    ICON Strategic Solutions    Phoenix, AZ 85067
     Posted about 2 hours    

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. General Summary The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements. Primary Responsibilities + Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs, and study processes. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructions to site personnel and study close out. + Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. + Ensures the integrity of clinical data and that the study is conducted in compliance with the approved protocol, GCP, applicable regulations, and SOPs. + Manages the investigative site staff to facilitate trial deliverables, e.g., subject enrollment, data deliverables. + Verifies proper management and accountability of Investigational Product (IP). + Writes and submits reports of investigational site findings and updates applicable tracking systems. Escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. + Manages essential documents as required by local regulations and ICH-GCP guidelines before, during, and after a clinical study; assists with resolution of investigational site/data queries. + Performs key risk assessment and management responsibilities throughout the project, including key risk indicator and site health analysis, site process evaluation, and project escalation. + Participates in audit preparation and follow-up activities as needed. Level-Specific Responsibilities: + Independently performs a variety of onsite and offsite monitoring visit types. + Gathers and reviews information for assigned sites and identifies inconsistencies. With limited guidance from project and functional management, assesses risk and escalates as appropriate. + Assists with non-complex ad hoc, short-term assignments in support of additional studies or departmental initiatives. + May serve as preceptor, providing training to less experienced clinical team members + 2 years of experience supporting clinical trials including 1 year of on-site monitoring experience + In-depth knowledge of the drug development process + In-depth knowledge and practical utilization of ICH- GCP and applicable regulatory requirements + Sound knowledge of applicable policies and procedures, SOPs, work instructions and other guidance documents + Good spoken and written communication skills; good presentation skills + Strong interpersonal, collaboration and time management skills + High proficiency with Microsoft Office and company collaboration applications + Excellent skill in the utilization of applicable clinical systems + Excellent critical thinking skills + Excellent organizational skills + Ability to focus on detail for extended periods of time; high attention to accuracy + Ability to travel extensively + Ability to establish and maintain effective working relationships with investigative site staff Education: + Undergraduate degree or international equivalent in clinical, science, or health-related field from an accredited institution; health care professional licensure, i.e., registered nurse + Equivalent combination of education, training and relevant experience may be considered in place of the education and experience stated above. All employees must read, write and speak fluent English and host country language. Benefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.


    Employment Type

    Full Time

  • Clinical Research Associate - Home-Based (Northeast/Boston)
    ICON Strategic Solutions    Phoenix, AZ 85067
     Posted about 2 hours    

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. General Summary The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements. Primary Responsibilities + Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs, and study processes. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructions to site personnel and study close out. + Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. + Ensures the integrity of clinical data and that the study is conducted in compliance with the approved protocol, GCP, applicable regulations, and SOPs. + Manages the investigative site staff to facilitate trial deliverables, e.g., subject enrollment, data deliverables. + Verifies proper management and accountability of Investigational Product (IP). + Writes and submits reports of investigational site findings and updates applicable tracking systems. Escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. + Manages essential documents as required by local regulations and ICH-GCP guidelines before, during, and after a clinical study; assists with resolution of investigational site/data queries. + Performs key risk assessment and management responsibilities throughout the project, including key risk indicator and site health analysis, site process evaluation, and project escalation. + Participates in audit preparation and follow-up activities as needed. Level-Specific Responsibilities: + Independently performs a variety of onsite and offsite monitoring visit types. + Gathers and reviews information for assigned sites and identifies inconsistencies. With limited guidance from project and functional management, assesses risk and escalates as appropriate. + Assists with non-complex ad hoc, short-term assignments in support of additional studies or departmental initiatives. + May serve as preceptor, providing training to less experienced clinical team members + 2 years of experience supporting clinical trials including 1 year of on-site monitoring experience + In-depth knowledge of the drug development process + In-depth knowledge and practical utilization of ICH- GCP and applicable regulatory requirements + Sound knowledge of applicable policies and procedures, SOPs, work instructions and other guidance documents + Good spoken and written communication skills; good presentation skills + Strong interpersonal, collaboration and time management skills + High proficiency with Microsoft Office and company collaboration applications + Excellent skill in the utilization of applicable clinical systems + Excellent critical thinking skills + Excellent organizational skills + Ability to focus on detail for extended periods of time; high attention to accuracy + Ability to travel extensively + Ability to establish and maintain effective working relationships with investigative site staff Education: + Undergraduate degree or international equivalent in clinical, science, or health-related field from an accredited institution; health care professional licensure, i.e., registered nurse + Equivalent combination of education, training and relevant experience may be considered in place of the education and experience stated above. All employees must read, write and speak fluent English and host country language. Benefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.


    Employment Type

    Full Time

  • Sr. Clinical Research Associate - Medical Device - Midwest
    ICON Strategic Solutions    Phoenix, AZ 85067
     Posted about 2 hours    

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. What will you be doing? Expert Level - Medical Device • Works on multiple trials in different disease areas • Demonstrated leadership, through involvement in specific initiatives when needed, and/or SME to systems and/or processes • Mentors/coaches junior flex team • Acts as Lead SM-training other SMs on study • Develops site start up documents for studies including SIV agenda • Provides SM “voice” when reviewing study documents (e.g. Monitoring Guidelines) • Represents LTMs or SMs on SMTs/meetings • Takes over LTM role reports review (SQV, SMV, SCV) for sites assigned to other SMs from the same trial • Supports country budget development and/or contract negotiation in liaison with CCS colleagues • Assists with ASV Metrics/KPIs: Metrics/KPIs governing these services are outlined in the Quality Oversight Plan (QOP) document. Interfaces – Primary/Other: • Primary interfaces: Provider Functional Manager, Sponsor Point of Contact, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. • Other Interfaces: Study Responsible Physician, Regional Quality and Compliance. Manager/Specialist, Local Drug Safety Officer (where required) and Site Manager team; Investigators and their delegates at site (trial personnel including study coordinators, pharmacists, etc.). What do you need to have? + • BA/BS degree/Degree in a health or science related field or equivalent industry experience • Specific therapeutic area experience depending on the services need. • Working knowledge of ICH GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines. • Demonstrate proficiency in IT skills for appropriate software and company systems. • Willingness to travel with overnight stay away from home according to business needs. • Proficient in speaking and writing in English and the country language where services will be provided. Effective communication skills, oral and written. • Experience with monitoring and site management of complex Early Phase of clinical development, as applicable. • Minimum of 6 years clinical trial monitoring experience • Strong leadership skills + To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status. Benefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.


    Employment Type

    Full Time

  • Clinical Research Associate - Home Based (Western USA)
    ICON Strategic Solutions    Phoenix, AZ 85067
     Posted about 2 hours    

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. General Summary The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements. Primary Responsibilities + Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs, and study processes. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructions to site personnel and study close out. + Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. + Ensures the integrity of clinical data and that the study is conducted in compliance with the approved protocol, GCP, applicable regulations, and SOPs. + Manages the investigative site staff to facilitate trial deliverables, e.g., subject enrollment, data deliverables. + Verifies proper management and accountability of Investigational Product (IP). + Writes and submits reports of investigational site findings and updates applicable tracking systems. Escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. + Manages essential documents as required by local regulations and ICH-GCP guidelines before, during, and after a clinical study; assists with resolution of investigational site/data queries. + Performs key risk assessment and management responsibilities throughout the project, including key risk indicator and site health analysis, site process evaluation, and project escalation. + Participates in audit preparation and follow-up activities as needed. Level-Specific Responsibilities: + Independently performs a variety of onsite and offsite monitoring visit types. + Gathers and reviews information for assigned sites and identifies inconsistencies. With limited guidance from project and functional management, assesses risk and escalates as appropriate. + Assists with non-complex ad hoc, short-term assignments in support of additional studies or departmental initiatives. + May serve as preceptor, providing training to less experienced clinical team members + 2 years of experience supporting clinical trials including 1 year of on-site monitoring experience + In-depth knowledge of the drug development process + In-depth knowledge and practical utilization of ICH- GCP and applicable regulatory requirements + Sound knowledge of applicable policies and procedures, SOPs, work instructions and other guidance documents + Good spoken and written communication skills; good presentation skills + Strong interpersonal, collaboration and time management skills + High proficiency with Microsoft Office and company collaboration applications + Excellent skill in the utilization of applicable clinical systems + Excellent critical thinking skills + Excellent organizational skills + Ability to focus on detail for extended periods of time; high attention to accuracy + Ability to travel extensively + Ability to establish and maintain effective working relationships with investigative site staff Education: + Undergraduate degree or international equivalent in clinical, science, or health-related field from an accredited institution; health care professional licensure, i.e., registered nurse + Equivalent combination of education, training and relevant experience may be considered in place of the education and experience stated above. All employees must read, write and speak fluent English and host country language. Benefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.


    Employment Type

    Full Time

  • Lead Clinical Research Associate - Home-Based
    ICON Strategic Solutions    Phoenix, AZ 85067
     Posted about 2 hours    

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. Position Overview: The Lead Clinical Research Associate (LCRA) provides operational expertise and leadership to ensure the effective and efficient delivery of clinical site monitoring on our clinical trials. The LCRA is the key representative for clinical monitoring on the Study Team and under the direction of the Clinical Operations Study Lead (COSL), they provide leadership and direction to their assigned CRAs throughout the lifecycle of a study. The LCRA assesses clinical trial site performance, adequacy of monitoring activities, reviews monitoring visit reports and metrics, and proactively identifies and communicates site management and monitoring issues and risks to the COSL and Clinical Monitoring management team. The Lead CRA ensures the monitoring activities of their assigned study(s) are in accordance with sponsor policies and procedures, ICH/GCP and local regulations. The LCRA will report directly to the Associate Director, Clinical Monitoring. + The Lead CRA is responsible for the leadership of their assigned CRAs on a given study(s), driving the team to ensure study deliverables are met with efficiency and quality + Develops or contributes to the Clinical Monitoring Plan, monitoring tools, visit report annotations, and CRA training materials + Responsible for training the CRAs on the study and ensuring study training compliance is maintained + Reviews monitoring visit reports and metrics, including protocol deviations and follow-up items, to evaluate for compliance and trends, summarizing for the study team, escalating issues, and involved in the development of corrective and preventative actions, as needed + Responsible for reviewing clinical data (e.g. electronic case report forms, central laboratory data, risk based monitoring outputs, etc…) to ensure the CRAs are informed and managing their site’s data with quality and integrity + Responsible for ensuring CRAs maintain their sites as inspection ready, including the Trial Master File (TMF), for health authority inspections at all times + Conducts regular meetings with their CRA team and with individual CRAs to disseminate timely and relevant updates and best practices for consistency and efficiency + Conducts co-monitoring visits or other monitoring visits (site qualification visit, site initiation visit, interim monitoring visit, or close-out visit) as required by study needs + Works with the Clinical Monitoring management team on developing and updating best practices and processes, with input on discussions around quality by design and operational delivery + Bachelors or equivalent degree required, preferably in life sciences, medicine or related discipline + Minimum of 5 years Clinical Research experience, with at least 3 years of experience in clinical site monitoring + Ability to travel up to 30% of the time + Fundamental knowledge of Clinical Research, and expertise in all phases of clinical trials; comprehensive knowledge and understanding of ICH-GCP + Strong knowledge of clinical trial systems, e.g. electronic case report forms, electronic Trial Master File, and Clinical Trial Management System + Excellent management skills with a remote team, developed with a collaborative approach to problem solving, driving performance and success in a global environment + Proven effectiveness as a team leader + Outstanding interpersonal, oral and written communication skills with the ability to communicate persuasively and with clarity, flexibility and adaptability to changing requirements, resourcefulness and creativity + Demonstration of successful execution of programs in a fast-paced environment managing multiple priorities Benefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.


    Employment Type

    Full Time

  • Clinical Research Associate 2
    ICON Strategic Solutions    Phoenix, AZ 85067
     Posted about 2 hours    

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. What will you be doing? As a Clinical Research Associate, you will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements. + Applies knowledge of ICONs policies and procedures + Demonstrates excellent written and oral communication + Demonstrates excellent knowledge of ICH/GCP + Displays ability to manage investigative sites to facilitate trial deliverables + Demonstrates ability to escalate issues appropriately + Conducts monitoring to confirm subject safety and data integrity + Describes and demonstrates the principals of IP accountability + Identifies scientific misconduct at the site level + Demonstrates working knowledge of Microsoft Office applications, Clinical Trial Management Systems, IVRS/IWRS and Electronic Data Capture platforms + Mentors CRAs new to the position or company + Serves as an observation visit leader + Conducts monitoring evaluation visits + Assists team lead in the development of trial tools or documents What do you need to have? Education: Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required Skills: + Read, write and speak fluent English; fluent in host country language required. + Knowledge of ICH and local regulatory authority regulations regarding drug + Clinical research experience + Knowledge of ICH and local regulatory authority regulations regarding drug + An advanced degree (e.g., M.S., M.B.A., PharmD, etc) + Experience in monitoring all trial components (PSSV to COV) + Experience in coaching/mentoring other CRAs + Oncology experience - Preferred- Opportunity for Oncology Training + To qualify, applicants must be legally authorized to work in the United States or Canada, and should not require, now or in the future, sponsorship for employment visa status. Benefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.


    Employment Type

    Full Time

  • Senior Clinical Research Associate - Medical Device - MW/NE
    ICON Strategic Solutions    Phoenix, AZ 85067
     Posted about 2 hours    

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. What will you be doing? Expert Level - Medical Device • Works on multiple trials in Orthopedic Medical Device • Demonstrated leadership, through involvement in specific initiatives when needed, and/or SME to systems and/or processes • Mentors/coaches junior flex team • Acts as Lead SM-training other SMs on study • Develops site start up documents for studies including SIV agenda • Provides SM “voice” when reviewing study documents (e.g. Monitoring Guidelines) • Represents LTMs or SMs on SMTs/meetings • Takes over LTM role reports review (SQV, SMV, SCV) for sites assigned to other SMs from the same trial • Supports country budget development and/or contract negotiation in liaison with CCS colleagues • Assists with ASV Metrics/KPIs: Metrics/KPIs governing these services are outlined in the Quality Oversight Plan (QOP) document. Interfaces – Primary/Other: • Primary interfaces: Provider Functional Manager, Sponsor Point of Contact, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. • Other Interfaces: Study Responsible Physician, Regional Quality and Compliance. Manager/Specialist, Local Drug Safety Officer (where required) and Site Manager team; Investigators and their delegates at site (trial personnel including study coordinators, pharmacists, etc.). What do you need to have? + • BA/BS degree/Degree in a health or science related field or equivalent industry experience • Specific therapeutic area experience depending on the services need. • Working knowledge of ICH GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines. • Demonstrate proficiency in IT skills for appropriate software and company systems. • Willingness to travel with overnight stay away from home according to business needs. • Proficient in speaking and writing in English and the country language where services will be provided. Effective communication skills, oral and written. • Experience with monitoring and site management of complex Early Phase of clinical development, as applicable. • Minimum of 6 years clinical trial monitoring experience • Strong leadership skills + To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status. Benefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.


    Employment Type

    Full Time

  • Clinical Research Associate -Oncology/Multi TA - Michigan
    ICON Strategic Solutions    Phoenix, AZ 85067
     Posted about 2 hours    

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. What you will be doing: The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements. - Monitoring Oncology and Multi -Therapeutic studies What you need to have: + B.A./B.S. with strong emphasis in science and/or biology preferred (but not required) + 2+ years of clinical monitoring experience required. 5 yrs of clinical monitoring preferred + Knowledge of ICH and local regulatory authority regulations regarding drug (PREFERRED) + Oncology experience preferred but not required + All therapeutic experience is welcome including but not limited to: Oncology, Hematology, Respiratory, Cardiovascular, Pain, CNS, Infectious Disease, Metabolism, Vaccines, Transplant and Ophthalmology + 8 visits/month, combo of on site and remote visits + To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status Benefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.


    Employment Type

    Full Time

  • Clinical Research Associate - Phase I - Home-Based (Kansas, Nebraska, Utah)
    ICON Strategic Solutions    Phoenix, AZ 85067
     Posted about 2 hours    

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. General Summary The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements. Primary Responsibilities + Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs, and study processes. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructions to site personnel and study close out. + Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. + Ensures the integrity of clinical data and that the study is conducted in compliance with the approved protocol, GCP, applicable regulations, and SOPs. + Manages the investigative site staff to facilitate trial deliverables, e.g., subject enrollment, data deliverables. + Verifies proper management and accountability of Investigational Product (IP). + Writes and submits reports of investigational site findings and updates applicable tracking systems. Escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. + Manages essential documents as required by local regulations and ICH-GCP guidelines before, during, and after a clinical study; assists with resolution of investigational site/data queries. + Performs key risk assessment and management responsibilities throughout the project, including key risk indicator and site health analysis, site process evaluation, and project escalation. + Participates in audit preparation and follow-up activities as needed. Level-Specific Responsibilities: + Independently performs a variety of onsite and offsite monitoring visit types. + Gathers and reviews information for assigned sites and identifies inconsistencies. With limited guidance from project and functional management, assesses risk and escalates as appropriate. + Assists with non-complex ad hoc, short-term assignments in support of additional studies or departmental initiatives. + May serve as preceptor, providing training to less experienced clinical team members + 2 years of experience supporting clinical trials including 1 year of on-site monitoring experience + In-depth knowledge of the drug development process + In-depth knowledge and practical utilization of ICH- GCP and applicable regulatory requirements + Sound knowledge of applicable policies and procedures, SOPs, work instructions and other guidance documents + Good spoken and written communication skills; good presentation skills + Strong interpersonal, collaboration and time management skills + High proficiency with Microsoft Office and company collaboration applications + Excellent skill in the utilization of applicable clinical systems + Excellent critical thinking skills + Excellent organizational skills + Ability to focus on detail for extended periods of time; high attention to accuracy + Ability to travel extensively + Ability to establish and maintain effective working relationships with investigative site staff Education: + Undergraduate degree or international equivalent in clinical, science, or health-related field from an accredited institution; health care professional licensure, i.e., registered nurse + Equivalent combination of education, training and relevant experience may be considered in place of the education and experience stated above. All employees must read, write and speak fluent English and host country language. Benefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.


    Employment Type

    Full Time


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