RWE Associate Clinical Project Manager – FSP

IQVIA

Durham, NC

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JOB DETAILS

SALARY

$68,400–$171,000 Per Year

SKILLS

Best Practices, Biology, Biotech and Pharmaceutical, Change Control, Change Management, Clinical Practices/Protocols, Clinical Research, Clinical Trial, Clinical Trial Management, Communication Skills, Contract Requirements, Corrective Action, Customer Support/Service, Detail Oriented, English Language, Establish Priorities, Forecasting, GCP (Good Clinical Practices), Healthcare, ICH Regulations, Leadership, Medical Treatment, Oncology, Operational Strategy, Patient Care, Presentation/Verbal Skills, Problem Solving Skills, Process Management, Project Planning, Project Tracking, Project/Program Management, Regulations, Regulatory Compliance, Regulatory Requirements, Risk Analysis, Standard Operating Procedures (SOP), Team Player, Time Management, Vendor/Supplier Management, Virology, Writing Skills

LOCATION

Durham, NC

POSTED

11 days ago

**_Job Overview_** _IQVIA is hiring to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent Pharma company. Associate Clinical Project Managers (aCPM) are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The aCPM is a member of the core project team responsible for project delivery of clinical and RWE studies across three therapeutic areas (oncology, virology, inflammation) to meet contractual requirements in accordance with SOPs, policies and practices. The aCPM supports the efforts of the Operations Lead and Project Managers to drive operational excellence and strategic leadership with our customers._ **_Essential Functions_** _• Provide input into the development of integrated study management plans with the core project team and/or sub-team._ _• Accountable for assigned portion of clinical studies while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with client standard processes, policies and procedures._ _• Collaborate with other functional groups where necessary to support milestone achievement and to manage study issues and obstacles._ _• Monitor progress and prepare/present project and/or sub-team information proactively to internal stakeholders. Support the project leader to prepare/present project and/or sub-team information proactively to external stakeholders._ _• Identify risk (positive and negative) and contingencies and partner with project leader in problem solving and resolution efforts._ _• Achieve project quality by identifying quality risks and issues, responding to issues raised by project sub-team members and partner with project leader planning/implementing appropriate corrective and preventative action plans._ _• May serve as primary (for small projects) or back-up project contact with customer._ _• Lead the efforts of a project sub-team, responsible for managing cross-collaboration of the sub-team to support milestone achievement and to manage issues and obstacles._ _• Support the project leader in ensuring the financial success of the project._ _• Forecast and identify opportunities to accelerate activities, build best practices, and transition knowledge from clinical to RWE pipeline_ _• Identify changes in scope and partner with project leader to manage change control process as necessary._ _• Identify lessons learned and implement best practices._ _• May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements_ **_Qualifications_** _• Associate's Degree In life sciences or related field required Req Or_ _• Bachelor's Degree In life sciences or related field required Req_ _• 2 years clinical research experience Req_ _• Requires intermediate level knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education combined with experience.; Req_ _• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge, therapeutic knowledge desired.;_ _• Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills._ _• Problem solving - Strong problem solving skills._ _• Organisation - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances._ _• Prioritisation - Ability to handle conflicting priorities._ _• Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output._ _• Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients. Strong customer service skills._ _• Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences._ IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $68,400.00 - $171,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled

About the Company

IQVIA

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. Healthcare is an industry designed to help humans. As a global community, we continuously invest and commit to advancing human health. To deliver value and real outcomes. To rise to the challenge to find the next breakthrough by making the most of increasingly limited resources. We are inspired by the potential and propelled by the possibilities. We share the vision to drive healthcare forward. To see how we can help accelerate progress and achievements. Others are developing these medical breakthroughs. We do our part by using breakthroughs in insights, technology and human intelligence to reimagine and deliver ways to help make them a reality. It’s bigger than better clinical trials. Or advances in technologies and analytics. Or faster insights. It’s about exploring a new path to better health outcomes via Human Data Science. It’s about harnessing the power of the IQVIA CORE™ to channel the insights, commercial and scientific depth, and executional expertise that drive maximum value for our customers. Motivated by the industry we help, we’re committed to providing solutions that enable life sciences companies to innovate with confidence, maximize opportunities, and, ultimately, drive human health outcomes forward.

COMPANY SIZE

10,000 employees or more

INDUSTRY

Healthcare Services

FOUNDED

1982

WEBSITE

https://www.iqvia.com/