Mcccd pipelineaz com

Business, Entrepreneurialism, and Management

Market Research Analysts and Marketing Specialists

Research market conditions in local, regional, or national areas, or gather information to determine potential sales of a product or service, or create a marketing campaign.

Salary Breakdown

Market Research Analysts and Marketing Specialists

Average

$63,680

ANNUAL

$30.61

HOURLY

Entry Level

$29,040

ANNUAL

$13.96

HOURLY

Mid Level

$67,405

ANNUAL

$32.41

HOURLY

Expert Level

$105,770

ANNUAL

$50.85

HOURLY


Current Available

Market Research Analysts and Marketing Specialists

656

Current Available Jobs


Top Expected Tasks

Market Research Analysts and Marketing Specialists


Knowledge, Skills & Abilities

Market Research Analysts and Marketing Specialists

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

KNOWLEDGE

English Language

KNOWLEDGE

Customer and Personal Service

KNOWLEDGE

Administration and Management

KNOWLEDGE

Sales and Marketing

KNOWLEDGE

Computers and Electronics

SKILL

Reading Comprehension

SKILL

Active Listening

SKILL

Complex Problem Solving

SKILL

Writing

SKILL

Speaking

ABILITY

Written Comprehension

ABILITY

Written Expression

ABILITY

Oral Comprehension

ABILITY

Oral Expression

ABILITY

Deductive Reasoning


Job Opportunities

Market Research Analysts and Marketing Specialists

  • IT Project Manager
    ICF    Phoenix, AZ 85067
     Posted about 2 hours    

    At ICF, we are fearless in finding new ways to solve problems, relentless in making sure it pays off for our clients and committed to making a positive change in the world. Join our community of management consultants, mission-driven technologists, data scientists, innovation researchers, CIO strategists, and public health researchers & evaluators to challenge the status quo. As we continue to expand our services and to support this growth, we are looking for a Management Consultant to join our Public Health Informatics and Technology business (PHIT). We provide technical assistance services to US Civilian Federal Agencies and their partners, such as the Centers for Disease Control and Prevention (CDC), National Center for Health Statistics (NCHS), Substance Abuse and Mental Health Services Administration (SAMHSA), and the Defense Health Agency (DHA).We are looking for a mid-and senior-level IT Project Managers who are customer focused and passionate about helping large government agencies modernize and transform through pragmatic enterprise strategies. The projects and services support the CDC meet the objectives of the agencies Data Modernization Initiative (DMI). You will be working on multiple projects at a time, interacting with all levels of ICF staff and stakeholders. The IT Project Manager will support tasks within the software development cycle and be responsible for system data together with the business intelligence it provides. Support project delivery on IT projects for the energy efficiency and utility sectors, including partnering with ICF subject matter experts on project execution.

    Key responsibilities:

    + This position is client facing and you will be responsible for assisting with the planning, execution, and monitoring of the team’s activities across multiple work streams, as well as advising on the strategic approach of the program.

    + Support all aspects of the software development cycle including requirements, design, testing, and delivery of energy efficiency tracking and reporting tools.

    + Work with stakeholders of IT systems to define the system requirements and design approach.

    + Develop an understanding of the client processes and procedures and assist with making improvements relative to technology.

    + Work with a team of senior technologists and to deliver solutions for clients.

    + Support users through training, as well as provide one-on-one technical assistance

    Mid-level: 2-3 yearsSenior-level: 4-5 years

    Required Skills include:

    + Provide Project Management support for a major, highly visible data classification and protection project.

    + Bachelor's degree

    + 8+ years of related IT technical project management experience leading complex, enterprise-level, IT-focused projects involving multiple stakeholders with diverse business needs.

    + Experience in identifying and bringing business analysis, project management and project implementation best practices, while championing innovation and out-of-the-box thinking to solving organizational problems

    + Ability to work within and lead and coordinate the activities of a medium-sized team of technical business analysts, data analysts, and technical SMEs

    + Knowledge and experience with full SDLC using both Waterfall and Agile methodologies

    + Ability to obtain and maintain a government security clearance

    + Agile Experience

    Working at ICF

    Working at ICF means applying a passion for meaningful work with intellectual rigor to help solve the leading issues of our day. Smart, compassionate, innovative, committed, ICF employees tackle unprecedented challenges to benefit people, businesses, and governments around the globe. We believe in collaboration, mutual respect, open communication, and opportunity for growth.

    We can only solve the world's toughest challenges by building an inclusive workplace that allows everyone to thrive. We are an equal opportunity employer, committed to hiring regardless of any protected characteristic, such as race, ethnicity, national origin, color, sex, gender identity/expression, sexual orientation, religion, age, disability status, or military/veteran status. Together, our employees are empowered to share their expertise and collaborate with others to achieve personal and professional goals. For more information, please read our EEO & AA policy (https://www.icf.com/legal/equal-employment-opportunity) .

    COVID-19 Policy: New or prospective U.S. employees must provide proof of complete vaccination on the date of their commencement of employment. If selected for employment, you will provide proof of your full vaccination status, defined as vaccinated two weeks after receiving the requisite number of doses of a COVID-19 vaccine approved or authorized for emergency use by the FDA.

    Reasonable Accommodations are available, including, but not limited to, for disabled veterans, individuals with disabilities, and individuals with sincerely held religious beliefs, in all phases of the application and employment process. To request an accommodation please email icfcareercenter@icf.com and we will be happy to assist. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodations. Read more about non-discrimination: EEO is the law (https://www.eeoc.gov/sites/default/files/migrated\_files/employers/poster\_screen\_reader\_optimized.pdf) and Pay Transparency Statement (https://www.dol.gov/sites/dolgov/files/ofccp/pdf/pay-transp\_English\_unformattedESQA508c.pdf) .

    Pay Range - There are multiple factors that are considered in determining final salary for a position, including, but not limited to, relevant work experience, skills, certifications and competencies that align to the specified role, geographic location, education and certifications as well as contract provisions regarding labor categories that are specific to the position. The salary range for Colorado is -

    Nationwide Remote Office (US99)


    Employment Type

    Full Time

  • Junior Technical Project Manager - Remote
    ICF    Phoenix, AZ 85067
     Posted about 2 hours    

    *We are open to supporting 100% remote work anywhere within the US.*

    Here’s your chance to join our award-winning agency, ICF Next. We’re changemakers, a community of mission driven creatives, communicators, strategists, and technologists. As a Junior Technical Project Manager within our Client Strategy and Loyalty team, you’ll be responsible for bringing our global teams together collaboratively using design thinking combined with a natural curiosity to deliver multiple projects that create experience-led transformation for our clients and their customers.

    If you’re passionate about growing client relationships and leading project teams from project planning through final delivery, we’d love to talk to you. This is a dynamic position and requires an individual with strong communication and collaboration skills who can think strategically and execute tactically. We are looking for a candidate to embrace the ambiguity in order to translate client requirements using agile delivery framework to deliver minimum viable products that can go to market with speed. Our new team member will be a strategic problem-solver that has a willingness to learn and grow with our team and be part of our journey to agile delivery.

    Essential Duties/Responsibilities

    + Ability to work in a matrixed mode and lead cross disciplinary teams, to develop, iterate, and refine technical solutions.

    + Actively communicate with clients to understand and define current needs and priorities.

    + Work collaboratively across disciplines to effectively scope and scale our delivery framework.

    + Establish and maintain schedules, roadmaps, and release plans in accordance with customer and stakeholder needs.

    + Work effectively with our strategists and clients to develop a prioritized backlog (experience with Product Increment planning preferred).

    + Schedule and drive effective agile ceremonies virtually and globally (e.g. backlog refinement, sprint planning, story point estimation, daily stand ups, sprint demos, retrospectives, inspect and adapt).

    + Build strong relationships with our clients to assure that the solution is understood and communicate relevant project information (e.g. status, risk, issues, deliverables).

    + Manage budgets, prepare cost estimates, and track resources using financial management tools.

    + Perform continuous risk assessment and mitigation; work with management to identify and remove resource, feasibility, and technical barriers that can impede development.

    + Maintain a positive, results-oriented work environment by building partnerships with internal and external partners.

    + Foster a culture of creativity, collaboration, innovation, and excellence in the work environment and continuously elevate the quality and caliber of the organization.

    + Manage projects independently, be self-motivated to identify and manage risks, and committed to achieving project goals and milestones.

    + Basic Qualifications:

    + Education: Bachelor’s degree or 4 additional years of professional experience

    + 3+ years project management experience leading digital development efforts

    + Preferred Qualifications:

    + 3+ years of consulting agency experience in a similar role highly preferred

    + Client strategy and loyalty marketing experience

    + Certified Scrum Master preferred

    + PMP certification

    + SAFE certification

    + Competent understanding of agile project management methodologies and principles

    + Demonstrated experience with the software development cycle including working with cross disciplinary teams, including strategy, UX and engineering

    + Ability to provide technical strategic guidance to the customer and project team

    + Experience launching digital solutions, including ongoing analysis and continuous product improvements

    + Working knowledge of the technical software development process, Agile delivery methods including Agile Scrum and/or Kanban

    + Proficiency working with JIRA and Confluence

    + Team player with excellent problem-solving and consensus-building skills

    + Ability to effectively work remotely with minimal supervision

    + Excellent communications skills, both written and verbal

    + Ability to influence and achieve results through effective negotiation and problem solving

    Working at ICF

    Working at ICF means applying a passion for meaningful work with intellectual rigor to help solve the leading issues of our day. Smart, compassionate, innovative, committed, ICF employees tackle unprecedented challenges to benefit people, businesses, and governments around the globe. We believe in collaboration, mutual respect, open communication, and opportunity for growth.

    We can only solve the world's toughest challenges by building an inclusive workplace that allows everyone to thrive. We are an equal opportunity employer, committed to hiring regardless of any protected characteristic, such as race, ethnicity, national origin, color, sex, gender identity/expression, sexual orientation, religion, age, disability status, or military/veteran status. Together, our employees are empowered to share their expertise and collaborate with others to achieve personal and professional goals. For more information, please read our EEO & AA policy (https://www.icf.com/legal/equal-employment-opportunity) .

    COVID-19 Policy: New or prospective U.S. employees must provide proof of complete vaccination on the date of their commencement of employment. If selected for employment, you will provide proof of your full vaccination status, defined as vaccinated two weeks after receiving the requisite number of doses of a COVID-19 vaccine approved or authorized for emergency use by the FDA.

    Reasonable Accommodations are available, including, but not limited to, for disabled veterans, individuals with disabilities, and individuals with sincerely held religious beliefs, in all phases of the application and employment process. To request an accommodation please email icfcareercenter@icf.com and we will be happy to assist. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodations. Read more about non-discrimination: EEO is the law (https://www.eeoc.gov/sites/default/files/migrated\_files/employers/poster\_screen\_reader\_optimized.pdf) and Pay Transparency Statement (https://www.dol.gov/sites/dolgov/files/ofccp/pdf/pay-transp\_English\_unformattedESQA508c.pdf) .

    Pay Range - There are multiple factors that are considered in determining final salary for a position, including, but not limited to, relevant work experience, skills, certifications and competencies that align to the specified role, geographic location, education and certifications as well as contract provisions regarding labor categories that are specific to the position. The salary range for Colorado is -

    Nationwide Remote Office (US99)


    Employment Type

    Full Time

  • Clinical Project Manager - Oncology Cell Therapy (US Remote)
    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. ICON is searching for CTM's in all Regions of US. The position is home-based. Responsibiliti es: As a Clinical Trial Manager (CTM), you have a wide range of responsibiliti es. We’re including a few of the big ones. Primarily, you will work to achieve the most successful clinical trial possible. You will lead cross-function al teams with Project Management, Clinical Operations, and Regulatory Affairs, while understanding and managing client expectations. You will proactively identify, resolve/mitiga te, and escalate risks or issues when necessary. • Provide Project Oversight and Leadership for Clinical Deliverables • Project Resourcing • Quality – Training & Development • Project Finance • Customer Relations (Internal & External) Requirements: •Prefer BS/BA or RN •Prefer CRO experience vs Pharma •Minimum of 3 years of clinical management experience (Clinical Trial Manager, Project Manager, Clin Ops Lead) •Global or regional experience •Management experience from start-up to database lock •Budget/financ e experience is required, resourcing focused tasks •Will typically take on 1-2 protocols at a time, depending on # of site and countries, but sometimes 3 protocols (usually sister studies •Must have experience developing Clinical Monitoring Plans, Data Cleaning Plans, CRA Data Entry Guidelines, etc. •Vendor management experience is preferred but not required • Oncology experience is a must (Cell or Gene therapy preferred) •Nice to have: pediatric oncology or biosimilars experience •Phase 1-3


    Employment Type

    Full Time

  • IRT Project Manager
    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. The IRT Project Manager assumes responsibility for operational execution of the IRT system used in clinical studies in development phases I to IV within clinical operations and oncology development operations. The IRT is a critical system in ensuring safety of all patients taking investigational medicinal product (IMP,) and if not set-up correctly, could jeopardize the usability of data obtained within the clinical studies. As an expert in IRT, the Project Manager leads the set-up and testing of the system, ensuring it meets the requirements of the clinical study protocol and that all associated processes are fully compliant with GxP regulations. The Project Manager continues to assume accountability of the IRT during the system’s life cycle, implementing all required amendments. The Project Manager is also responsible for implementing the clinical supply chain within the IRT for global clinical studies together with the Clinical Supply Manager and ensures the IRT settings allow for optimal stock of IMP for study sites to allocate to patients. Furthermore, the Project Manager is responsible for IMP drug handling training to external investigational sites and internal functions such as CRAs to ensure regulatory GCP compliance. Key Tasks & Responsibilities: + Revises / develops the clinical study protocol with particular focus on the attributes of study drugs including comparators, medical devices, randomization and blinding. + Ensures appropriate supply of study medication for all patients in a clinical trial by implementing optimal IRT supply strategies. + For studies without an IRT, the Project Manager monitors and assesses clinical supply demands to ensure requirements are met. They are also responsible for the supervision of the distribution of clinical supplies from central to local depots and from depots to sites. + Responsible and accountable for assessing the usability of study medication that has been affected by a temperature excursion at site, in co-operation with QA, to ensure that if a drug’s pharmaceutical quality has been compromised it cannot be taken by patients. + Responsible for expiry date management of study medication on the study level and for taking appropriate action to prevent patients taking expired medication. If the shelf life of a batch of study medication can be extended, the Project Manager initiates and supervises the process of labeling IMP with the new expiry date in accordance with the applicable GMP regulations and legal requirements. + Provides guidance on correct storage of study medication according to the applicable Technical Registration Documents. + Support CRA’s with drug accountability activities. + Leads the IRT cross-functional sub-team and is accountable for the set-up and maintenance of the IRT System with special attention to the proper and correct supply of study sites with study medication, including the correct drug dispensation according to the study protocol. + Provides input on IRT supplier selection and performs on-going IRT supplier oversight such as performance management and issue resolution for their assigned studies. + Responsible for providing guidance and training to study teams, CRAs and site personnel on the handling of study medication and the IRT System. + Creates and maintains drug handling instructions / pharmacy manual if required. + Ensures compliance with all relevant SOPs, GMP, GCP and ICH guidelines, as well as with legal and ethical standards. Qualifications & Competencies: + Bachelor’s Degree or equivalent. Pharmacist degree preferred + 5 years of relevant healthcare clinical development experience + Profound knowledge in drug development + Profound knowledge in setting up Interactive Response (IRT) Systems + Profound knowledge in GCP and knowledge of GMP + Excellent project management skills + Excellent communication skills (including fluent English) + Excellent presentation skills 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 Project Manager - Oncology Cell Therapy (US Remote)
    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. ICON is searching for CTM's in all Regions of US. The position is home-based. Responsibiliti es: As a Clinical Trial Manager (CTM), you have a wide range of responsibiliti es. We’re including a few of the big ones. Primarily, you will work to achieve the most successful clinical trial possible. You will lead cross-function al teams with Project Management, Clinical Operations, and Regulatory Affairs, while understanding and managing client expectations. You will proactively identify, resolve/mitiga te, and escalate risks or issues when necessary. • Provide Project Oversight and Leadership for Clinical Deliverables • Project Resourcing • Quality – Training & Development • Project Finance • Customer Relations (Internal & External) Requirements: •Prefer BS/BA or RN •Prefer CRO experience vs Pharma •Minimum of 3 years of clinical management experience (Clinical Trial Manager, Project Manager, Clin Ops Lead) •Global or regional experience •Management experience from start-up to database lock •Budget/financ e experience is required, resourcing focused tasks •Will typically take on 1-2 protocols at a time, depending on # of site and countries, but sometimes 3 protocols (usually sister studies •Must have experience developing Clinical Monitoring Plans, Data Cleaning Plans, CRA Data Entry Guidelines, etc. •Vendor management experience is preferred but not required • Oncology experience is a must (Cell or Gene therapy preferred) •Nice to have: pediatric oncology or biosimilars experience •Phase 1-3


    Employment Type

    Full Time

  • IVRS Project Manager
    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. Responsible for providing end-to-end IVRS support to clinical project teams including but not limited to gathering study specific IVRS user requirements, creating and enforcing IVRS standards, managing vendor performance, monitoring system change requests, and supporting training & education for stakeholders. + Execute IVRS development process from kickoff to system go live, ongoing system change control, and system closeout. + Work with the internal stakeholders and IVR vendors to develop study specific IVR requirements, creates and enforces the use of IVRS standards. Responsibilities may include collaboration with vendors and internal stakeholders to define requirements and develop implementation plans. Ensures adherence to IVRS standards, reviews study team business case proposals, and provides final go / no-go decision regarding requests to utilize custom functionality. + Manage vendor performance and relationship(s) at the study level. Responsibilities may include performing root cause analysis and identifying corrective/preventative actions, and serving as a point of escalation for vendor issues. + Ensure vendor system development processes align with Merck Quality and System Life Cycle expectations. + Monitor system change requests. Ensure adherence to IVRS standards, works with the clinical project team to identify system changes and ensure completion of the changes through its life-cycle. Monitors and analyzes system change requests, and identifies corrective actions for utilization of standards. + May provide support in the following areas: + data transfer issue resolution between IVRS vendors and shipping depots in support of shipping processes, DOF/ERP specifications, and issue resolution. + lock & transfer of allocation schedules to IVRS vendors, the requirement document approval process, or the provision of site & Merck user information to IVRS vendors. + development / maintenance of relevant documentation, including applicable SOPs, job aids, and guidance documents. + process improvement activities. + training and education for stakeholders including develop, or assist in development of, reference and/or training material; may provide cross-functional internal and external communication as needed. Education and Work Experience: + 2-4 years of experience in clinical supplies, clinical research, or database design & development + B.A./B.S. in biology, life sciences, computer science, or related field Knowledge, Skills, and Abilities: + Demonstrated knowledge of IVRS development processes. + High level understanding of clinical supply chain within the pharmaceutical industry. + Knowledge of databases, structure, & corresponding tools used to manage, extract, & report data. + Working knowledge of clinical development and statistical concepts. + Effective written and verbal communication skills. + Ability to organize and manage multiple tasks at one time and meet deadlines in a complex environment working both internal to Merck and external to Merck. + Average proficiency with Microsoft applications (Word, Excel, PowerPoint, Project). + Working knowledge of regulatory requirements (e.g., GMP), quality procedures and SOP execution. 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

  • IRT Project Manager
    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. Responsible for providing end-to-end IVRS support to clinical project teams including but not limited to gathering study specific IVRS user requirements, creating and enforcing IVRS standards, managing vendor performance, monitoring system change requests, and supporting training & education for stakeholders. + Execute IVRS development process from kickoff to system go live, ongoing system change control, and system closeout. + Work with the internal stakeholders and IVR vendors to develop study specific IVR requirements, creates and enforces the use of IVRS standards. Responsibilities may include collaboration with vendors and internal stakeholders to define requirements and develop implementation plans. Ensures adherence to IVRS standards, reviews study team business case proposals, and provides final go / no-go decision regarding requests to utilize custom functionality. + Manage vendor performance and relationship(s) at the study level. Responsibilities may include performing root cause analysis and identifying corrective/preventative actions, and serving as a point of escalation for vendor issues. + Ensure vendor system development processes align with Merck Quality and System Life Cycle expectations. + Monitor system change requests. Ensure adherence to IVRS standards, works with the clinical project team to identify system changes and ensure completion of the changes through its life-cycle. Monitors and analyzes system change requests, and identifies corrective actions for utilization of standards. + May provide support in the following areas: + data transfer issue resolution between IVRS vendors and shipping depots in support of shipping processes, DOF/ERP specifications, and issue resolution. + lock & transfer of allocation schedules to IVRS vendors, the requirement document approval process, or the provision of site & Merck user information to IVRS vendors. + development / maintenance of relevant documentation, including applicable SOPs, job aids, and guidance documents. + process improvement activities. + training and education for stakeholders including develop, or assist in development of, reference and/or training material; may provide cross-functional internal and external communication as needed. Education and Work Experience: + 2-4 years of experience in clinical supplies, clinical research, or database design & development + B.A./B.S. in biology, life sciences, computer science, or related field Knowledge, Skills, and Abilities: + Demonstrated knowledge of IVRS development processes. + High level understanding of clinical supply chain within the pharmaceutical industry. + Knowledge of databases, structure, & corresponding tools used to manage, extract, & report data. + Working knowledge of clinical development and statistical concepts. + Effective written and verbal communication skills. + Ability to organize and manage multiple tasks at one time and meet deadlines in a complex environment working both internal to Merck and external to Merck. + Average proficiency with Microsoft applications (Word, Excel, PowerPoint, Project). + Working knowledge of regulatory requirements (e.g., GMP), quality procedures and SOP execution. 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 Project Manager
    ICON Clinical Research    Phoenix, AZ 85067
     Posted about 2 hours    

    At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That’s our vision. We’re driven by it. And we need talented people who share it. If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. As Senior Project Manager, you will play a key role within ICON Central Labs by ensuring overall client happiness. You will be our client’s main contact for ICON's Central Laboratories’ services and providing day-to-day management of studies. As a trusted partner, you will attend client meetings to provide project updates. You will also be actively involved in training and mentoring junior members of the team. The Role • Acts as our clients contact person in all matters regarding our central laboratory services, following up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and the ICON Site Services Department. • Review newly assigned protocols and Amendments. Oversee and handle the completion of the Clinical Laboratory Worksheet. • Enter protocol parameter information into PACS//ICOLIMS and other systems for new and/or amended protocols. Preparing QC materials. • Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by crafting and updating the study specific Communication and Escalation Plan. Ensure adherence to the protocol specific monitoring plan. Maintaining study files and ensuring that all appropriate documents are properly maintained. Ensure that all necessary documents are archived at study closure. • Provide Sponsors with study management reports. • Dedicatedly monitor study budget. • Set the timelines for and monitor the progress of shipment requests for storage samples and verify data. • Attend and represent ICON at Sponsor Investigator Meetings, Kick-Off Meeting, Bid Defences or Initiations. • Develop new tools, train new employees • Performs additional relevant responsibilities as requested by management. What you need • 3-5 years’ work experience within a central laboratory environment OR extensive clinical laboratory experience. • Have a Degree in a Life Sciences or related discipline. • Customer focussed with the ability to build excellent rapport with business partners. • Excellent knowledge of Excel and PowerPoint. • Comfortable with presenting to groups. • Experience in attending Bid Defences. • Super organised and remains calm in taking care of multiple priorities and working to tight deadlines. • Passionate about developing a career within Project Management. Benefits of Working in ICON: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON 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 through the form below.


    Employment Type

    Full Time

  • Project Manager
    ICON Clinical Research    Phoenix, AZ 85067
     Posted about 2 hours    

    At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.That’s our vision. We’re driven by it. And we need talented people who share it.If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. Role: Project Manager Real World Evidence Location: Remote (US)Recognize, exemplify and adhere to ICON's values, which center on our commitment to People, Clients and Performance.• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.• Travel (approximately 20-30%) domestic and/or international. Travel to other sites within the network may be required to support increases in workload and, or studies/projects as needed.• Lead the planning and implementation of cross-functional project(s).• Facilitate the definition of project scope, goals and deliverables• Define project tasks and resource requirements.• Develop full-scale cross-functional project plans.• Assemble and coordinate project staff• Manage project budget• Plan and schedule project timelines• Develop and Manage Risk Mitigation Strategies for projects• Track project deliverables using appropriate tools• Provide direction and support to project team• Quality assurance• Constantly monitor and report on progress of the project to all stakeholders• Present reports defining project progress, problems and solutions.• Implement and manage project changes and interventions to achieve project outputs• Project evaluations and assessment of results• Other duties as assignedBenefits of Working in ICON:Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.ICON 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 through the form below.


    Employment Type

    Full Time

  • Senior Project Manager
    ICON Clinical Research    Phoenix, AZ 85067
     Posted about 2 hours    

    At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.That’s our vision. We’re driven by it. And we need talented people who share it.If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.As Senior Project Manager, you will play a key role within ICON Central Labs by ensuring overall client happiness. You will be our client’s main contact for ICON's Central Laboratories’ services and providing day-to-day management of studies. As a trusted partner, you will attend client meetings to provide project updates. You will also be actively involved in training and mentoring junior members of the team.The Role• Acts as our clients contact person in all matters regarding our central laboratory services, following up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and the ICON Site Services Department.• Review newly assigned protocols and Amendments. Oversee and handle the completion of the Clinical Laboratory Worksheet.• Enter protocol parameter information into PACS//ICOLIMS and other systems for new and/or amended protocols. Preparing QC materials.• Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by crafting and updating the study specific Communication and Escalation Plan. Ensure adherence to the protocol specific monitoring plan. Maintaining study files and ensuring that all appropriate documents are properly maintained. Ensure that all necessary documents are archived at study closure.• Provide Sponsors with study management reports.• Dedicatedly monitor study budget.• Set the timelines for and monitor the progress of shipment requests for storage samples and verify data.• Attend and represent ICON at Sponsor Investigator Meetings, Kick-Off Meeting, Bid Defences or Initiations.• Develop new tools, train new employees• Performs additional relevant responsibilities as requested by management.What you need• 3-5 years’ work experience within a central laboratory environment OR extensive clinical laboratory experience.• Have a Degree in a Life Sciences or related discipline.• Customer focussed with the ability to build excellent rapport with business partners.• Excellent knowledge of Excel and PowerPoint.• Comfortable with presenting to groups.• Experience in attending Bid Defences.• Super organised and remains calm in taking care of multiple priorities and working to tight deadlines.• Passionate about developing a career within Project Management.Benefits of Working in ICON:Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.ICON 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 through the form below.


    Employment Type

    Full Time


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