Evidence Generation Project Manager at ClinChoice

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Full Time

Start Date

Immediate

Expiry Date

07 Jan, 26

Salary

0.0

Posted On

09 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Project Management, Clinical Trials, Operational Excellence, Recruitment Tracking, Risk Mitigation, Stakeholder Management, GCP, ICH Guidelines, Real-World Evidence, Health Economics, Attention to Detail, Communication, Flexibility, Team Coordination, Dashboard Development, Timeline Management

Industry

Pharmaceutical Manufacturing

Description

Are you interested in partnering directly with a single sponsor while enjoying the stability, resources, and career growth opportunities that come with working for a global CRO? At ClinChoice, our team describes it as the best of both worlds. ClinChoice is seeking an Evidence Generation Project Manager to support one of our partner organizations - a leading global biopharmaceutical company at the forefront of biomedicine innovation. This role will focus on post-marketing and Phase IV clinical trials and offers a remote work arrangement with approximately 40% travel. It is a full-time (1.0 FTE), 1-year contract position, open to both freelancers and W-2 contractors. As a global, full-service CRO, ClinChoice is committed to quality, professional development, and a supportive, collaborative culture. In this client-facing role, we’re looking for a confident project manager who can work independently while fostering strong, trust-based relationships with client counterparts. Main Job Tasks and Responsibilities: Will report to the Director of Evidence Generation. Daily focus on operational excellence of all the post marketing clinical trials. Will be responsible for all timelines and execution planning of post marketing Phase 4 trials, RWE, HEOR etc. Recruitment timelines and acceleration planning for all studies and projects. Support coordination of execution at all levels for evidence generation. Someone with PM experience in clinical trials that is great at building trackers and leads without authority. Has 2-5 years of clinical trial project management experience. Can work in a very fast paced environment and keep track of 8-10 clinical trials at one time. Education and Experience: Bachelor’s degree in life sciences, public health, or related field required; advanced degree (MS, MPH, PharmD) preferred. 2–5 years of project management experience in clinical research, preferably within post-marketing (Phase IV), RWE, or HEOR studies. Proven ability to manage multiple (8–10) concurrent studies in a fast-paced, matrixed environment. Strong track record of operational excellence in clinical trial execution, including timeline management, recruitment tracking, and risk mitigation. Hands-on experience developing and maintaining project plans, dashboards, and trackers to drive accountability and transparency. Demonstrated ability to lead without direct authority, coordinating cross-functional teams and external vendors/CROs. Familiarity with GCP, ICH guidelines, and post-marketing evidence generation processes. Excellent organizational, communication, and stakeholder management skills. Comfortable working with ambiguity, shifting priorities, and competing deadlines while maintaining attention to detail. Flexibility to travel to the sites- 40%. The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for? About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. We are on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Join our passionate team and make a meaningful impact on global healthcare! Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset, and they are the fulcrum around which all ClinChoice activities are built, and close management and training is the core instrument to develop and maintain highly qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. Keywords: Evidence Generation, Evidence Project Manager, Real-World Evidence (RWE), Health Economics and Outcomes Research (HEOR), Post-Marketing Studies, Phase IV Clinical Trials, Observational Studies, Late Phase Research, Real-World Data (RWD), Non-Interventional Studies (NIS)

Responsibilities

The Evidence Generation Project Manager will focus on operational excellence for post-marketing clinical trials and will be responsible for timelines and execution planning. This role requires coordination of execution at all levels for evidence generation.