Job summary
Job post source
This job is directly from IQVIA
Job overview
The Clinical Project Manager (FSP) at IQVIA oversees a portfolio of observational studies, playing a key role in the Real World Solutions team to ensure successful project delivery and governance.
Responsibilities and impact
The role involves managing execution of high-priority studies, coordinating with stakeholders, leading global cross-functional teams, developing governance structures, monitoring progress and risks, managing budgets, and communicating updates to senior management.
Compensation and benefits
The base pay range is $93,100 to $232,800 annually, with potential bonuses, incentive plans, and a range of health and welfare benefits depending on the position.
Experience and skills
Candidates need a bachelor's degree in life sciences or related field, 2-4 years of project management experience in clinical operations, preferably with CRO experience, and in-depth knowledge of real-world evidence study designs.
Career development
IQVIA offers broad opportunities for career development within its global footprint and Real World Solutions team, supporting growth through diverse project experiences.
Work environment and culture
IQVIA promotes an inclusive work environment valuing diversity and equal opportunity, fostering collaboration in a matrix environment with autonomy.
Company information
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence, focused on accelerating medical treatment development and improving patient outcomes.
Team overview
The candidate will work with epidemiology and data science leads, vendors, and program leads within a multi-disciplinary team managing a portfolio of studies.
Unique job features
This role is distinguished by its focus on observational studies within real-world evidence, high-profile project management responsibilities, and leadership in governance processes.
Company overview
IQVIA is a global leader in advanced analytics, technology solutions, and contract research services for the life sciences industry. They generate revenue by providing data-driven insights and innovative solutions that help pharmaceutical, biotechnology, and medical device companies improve their clinical, commercial, and real-world operations. Formed through the merger of IMS Health and Quintiles in 2016, IQVIA combines deep domain expertise with advanced analytics to drive healthcare forward. Their extensive history and commitment to leveraging data and technology make them a pivotal player in enhancing patient outcomes and healthcare efficiency worldwide.
How to land this job
Position your resume to highlight your experience managing observational studies and your familiarity with real-world evidence study designs, as these are central to the Clinical Project Manager role at IQVIA.
Emphasize your ability to lead cross-functional teams, manage project timelines, anticipate risks, and communicate effectively with stakeholders including vendors and program leads.
Apply through multiple platforms such as the IQVIA corporate careers site, LinkedIn, and other job boards where IQVIA posts to maximize your application visibility.
Connect with current employees in IQVIA’s Real World Solutions or clinical project management teams on LinkedIn; when reaching out, mention your interest in observational research or recent IQVIA projects you found intriguing as ice breakers.
Optimize your resume for ATS by incorporating keywords from the job description like 'observational studies,' 'project management,' 'real-world evidence,' 'cross-functional collaboration,' and 'risk mitigation' to ensure it passes initial screenings.
Use Jennie Johnson’s Power Apply feature to automate tailoring your resume, applying through multiple channels, and identifying LinkedIn connections to network with, allowing you to focus more on preparing for interviews and career growth.
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