Clinical Trial Project Manager

Clinical Project Manager

Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring forward ideas that make a real difference. Be part of a mission-driven organization dedicated to advancing clinical research and transforming lives.

The Clinical Project Manager at WEP Clinical is responsible for the setup, implementation, and management of clinical trials, ensuring patient safety, data integrity, and high-quality delivery in compliance with applicable regulations. This role provides leadership across cross-functional teams, manages client relationships, and is accountable for delivering clinical trials on time, within scope, and within budget.

The Ideal Candidate:

• Adaptable
• Detail-oriented
• Collaborative
• Solutions-focused

What You'll Do:

The level of appointment (e.g., Project Manager II or Senior Project Manager) will be determined based on the candidate's experience, skills, and demonstrated capabilities during the interview process. Principal duties and responsibilities include:

• Leading the setup, execution, and close-out of clinical trials in compliance with WEP Clinical SOPs, GCP/ICH guidelines, and regulatory requirements.
• Providing day-to-day accountability for the operational delivery of assigned clinical trials.
• Developing and maintaining study manuals, operational project plans, timelines, and key performance metrics.
• Ensuring proper setup, maintenance, and close-out of eTMF and CTMS systems.

Leadership & Cross-Functional Oversight:

• Serving as project team lead and primary point of contact for internal and external stakeholders.
• Providing oversight and coordination of cross-functional deliverables including monitoring, site management, data management, pharmacovigilance, regulatory, IP supply, and medical writing.
• Ensuring internal and external teams are appropriately trained on study protocols and operational requirements.

Client & Stakeholder Management:

• Acting as the primary client contact for clinical trial operations, deliverables, and issue resolution.
• Leading internal and external meetings, ensuring alignment on project status, risks, and timelines.

Risk & Issue Management:

• Identifying, assessing, and proactively managing risks and issues throughout the clinical trial lifecycle.
• Implementing mitigation strategies and corrective actions where required.

Regulatory & Compliance:

• Overseeing submissions to IRB/ECs and review informed consent forms as required.
• Ensuring compliance with regulatory requirements and internal quality standards.
• Collaborating with Quality Assurance to support audits, CAPAs, and investigations as appropriate.

Financial & Vendor Management:

• Managing project budgets, scope, and financial performance.
• Overseeing vendor performance and deliverables, including review and approval of invoices.
• Reviewing site payments and ensuring alignment with Clinical Trial Agreements.

Documentation & Systems:

• Maintaining accurate and complete trial documentation within internal systems (e.g., SharePoint).
• Ensuring all trial records meet quality and compliance standards.

What You'll Need:

• Bachelor's Degree (health or science field preferred)
• Minimum 5 years' experience in a Project Manager role within clinical trials or clinical research
• Demonstrated experience managing clinical trials from initiation through close-out
• Strong working knowledge of ICH GCP guidelines and clinical trial processes
• Proven ability to lead cross-functional teams and manage multiple priorities
• Strong organizational, problem-solving, and decision-making skills
• Effective verbal and written communication skills
• Proficiency in Microsoft Office tools
• Ability and willingness to travel as required for business needs

Additional Notes:

• This role may be filled at different levels depending on experience and demonstrated capability.
• Responsibilities may expand in scope with increased seniority and complexity of assigned projects.

Location eligibility applies. Candidates must reside in a U.S. state where the company is authorized to hire. This role is not eligible for residents of: California, Colorado, New York, Washington, New Jersey, Massachusetts, Illinois, Hawaii, and District of Columbia.

What We Offer:

• Medical, dental, and vision insurance
• FSA, HSA
• Voluntary Critical Illness, Hospital Indemnity, and Accident Insurance
• Group short-term and long-term disability insurance
• Group Life Insurance
• 401K safe harbor plan and company match
• Paid vacation, holiday, sick and volunteer time
• Paid maternity & paternity leave

What Sets Us Apart:

WEP Clinical partners with biopharmaceutical Sponsors to help them bring treatments closer to the patients who need them most. Through end-to-end clinical trial delivery, home health services, expanded access programs, and market access consultancy, we provide flexible, fit-for-purpose solutions that support drug development, improve access, and help therapies reach the right patients at the right time. With more than 15 years of global experience, we have supported programs across 150+ countries, combining operational scale with the agility and personalized service of a specialized provider. Our work helps bridge critical gaps in care, ensuring safe, ethical, and efficient access to promising new treatments.

We're Committed to Our Team:

WEP has many initiatives to encourage wellness, growth and development, and team relationships. Check out our LinkedIn Life Page to learn more about our team events and all we do to support our employees.

How We Work at WEP Clinical:

At WEP Clinical, we look for individuals who are conscientious, exercise sound judgment, and engage with others thoughtfully and professionally. We believe excellence is achieved through integrity, accountability, and respect for diverse perspectives - and we are committed to helping our people grow and succeed in an inclusive, supportive environment.

Our Services Include:

• Access Programs
• Clinical Trial Services
• Patient Site Solutions
• Clinical Trial Supply
• Market Access and Commercialization

Data Privacy Notice:

WEP Clinical is committed to protecting your personal information throughout the recruitment process. By applying, you acknowledge that your personal data will be processed in accordance with our Privacy Policy and Job Applicant Privacy Notice.

Privacy Policy:

Job Applicant Privacy Notice:

How to Apply:

To be considered for this role, please submit your resume through the WEP Clinical Careers Portal or by using LinkedIn's Easy Apply option. Please ensure your resume is in English.

Important Note:

To streamline our hiring process, we use an Upwage AI screener. If you receive a link from Upwage, it is a legitimate part of our application process and helps ensure every candidate is reviewed consistently. If you are selected to move forward after the screener, a member of our team will contact you directly from an @wepclinical.com email address to guide you through the next steps of the interview process. Please ensure you apply only through our official careers page ( or our verified LinkedIn page.

For Your Safety, Please Note:

We will never communicate with you via Microsoft Teams or text message.

We will never ask for your bank account information at any stage of recruitment.

WEP Clinical is a smoke-free, drug-free, and alcohol-free work environment.

WEP Clinical is an equal-opportunity employer. WEP Clinical does not unlawfully discriminate against employees or applicants for employment based on an individual's race, color, religion, creed, sex, sexual orientation, gender identity or expression,