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Medical Affairs Project Manager Jobs (NOW HIRING)

Job OverviewThe Project Manager (PM) is part of the Medical Affairs team based in East Windsor, NJ, residing in Acrotech's home office headquarters and reporting to the Head of Medical Affairs. The ...

DEKA Research & Development has an immediate opening for a Regulatory Affairs Project Manager to contribute to a dynamic, medical device research and development environment. The individual in this ...

Project Management * Monitor and report on the progress of Medical Affairs projects and programs. With minimal direction provide support to complex, multi-stakeholder projects and programmes ...

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Medical Affairs Project Manager information

How does a Medical Affairs Project Manager typically collaborate with cross-functional teams within a pharmaceutical company?

A Medical Affairs Project Manager regularly works with diverse teams, including clinical development, regulatory affairs, commercial, and medical information. Collaboration often involves coordinating scientific communication, ensuring compliance with industry regulations, and supporting the launch of new products. This role acts as a liaison, facilitating the timely exchange of information and aligning project goals across departments. Effective communication and strong organizational skills are key to managing these collaborative efforts successfully.

What are the key skills and qualifications needed to thrive as a Medical Affairs Project Manager, and why are they important?

To thrive as a Medical Affairs Project Manager, you need a strong background in life sciences or pharmacy, experience in project management, and knowledge of medical regulatory standards. Familiarity with project management tools (like MS Project or Asana), medical information databases, and compliance systems is typically required, along with certifications such as PMP or PRINCE2. Excellent organizational abilities, cross-functional communication, and stakeholder management are crucial soft skills in this role. These skills and qualities ensure effective coordination of medical projects, regulatory compliance, and successful collaboration between clinical, regulatory, and commercial teams.

What does a Medical Affairs Project Manager do?

A Medical Affairs Project Manager oversees and coordinates medical and scientific projects within pharmaceutical, biotech, or healthcare organizations. They work closely with cross-functional teams to ensure the successful planning, execution, and completion of medical initiatives, such as clinical trials, medical education programs, or product launches. Their responsibilities include managing timelines, budgets, compliance, and communication among stakeholders to align projects with regulatory requirements and company goals. They also help translate complex scientific data into actionable strategies for both internal teams and external partners.
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What cities are hiring for Medical Affairs Project Manager jobs? Cities with the most Medical Affairs Project Manager job openings:
What states have the most Medical Affairs Project Manager jobs? States with the most job openings for Medical Affairs Project Manager jobs include:
Infographic showing various Medical Affairs Project Manager job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.
Regulatory & Medical Affairs - Project Manager

Regulatory & Medical Affairs - Project Manager

Eclaro

Lawrence Township, NJ

$75.83 - $80.43/hr

Other

Medical, Dental, Vision, Retirement

Posted 14 days ago


Job description

Regulatory & Medical Affairs - Project Manager Job Number: 26-00704 Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for a Regulatory & Medical Affairs - Project Manager for our client in Lawrence Township, NJ. ECLARO’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world.

If you’re up to the challenge, then take a chance at this rewarding opportunity! Position Overview: We are seeking a Senior Project Manager to join the Launch Excellence (Lx) team and support the end-to-end operations of the Lx capability. This is a highly cross-functional, senior-level role that blends strategic project management with hands-on operational execution across a dynamic, fast-paced launch environment.

The ideal consultant is a self-starter who thrives in collaborative settings, can seamlessly shift priorities based on business need, and brings a strong background in pharmaceutical or biotech commercial operations. This role requires someone who is equally comfortable driving meetings, managing complex PM documentation, supporting platform operations, and partnering with IT, commercial, and cross-functional matrix teams. Responsibilities: Lx Onboarding: Collaborate with Brand Leads and Launch Managers to schedule, align, and execute the Lx Onboarding training series, an Lx-integrated approach for kick-starting teams in their launch plan management.

Support the ongoing optimization of the Lx onboarding process to maximize stakeholder adoption and effective platform utilization. Maintain and document feedback loops to surface continuous improvement opportunities across the onboarding journey. Lx Operations: Manage Lx Playbook Launch Plan and User Activations across the organization.

Maintain and update the Lx Playbook Users Team Channel, including content governance and user list management. Administer Lx Playbook License Management, ensuring accurate tracking and allocation. Generate and distribute Lx Playbook Trends, Metrics, and Data reporting on a monthly and ad hoc basis.

Manage the Lx Mailbox, handling reactive user responses and general platform inquiries in a timely manner. Provide Lx Production Support, including troubleshooting, status calls, and operational issue resolution. Lx Project Management: Own and maintain core PM documentation including the PM Planner, RAID Log, and Tribeca / Lx Production Log.

Track and manage Lx Feedback, ensuring timely documentation and resolution. Maintain a current Resource Inventory and manage the Teams Posts Log. Meeting & Program Management Leadership: Lead the Weekly Program Management Meeting with Tribeca and the internal Lx team.

Participate and assist with the Weekly Lx Operational Connect with Smart Launch, driving agenda, facilitation, and follow-through. Own action item tracking and ensure cross-functional accountability across all Lx meetings and workstreams. SAMai Operations: Review and manage platform access.

Required Qualifications: 7 years of experience in project management, commercial operations, or launch operations within the pharmaceutical or biotech industry. Proven track record managing complex, multi-workstream programs in a senior capacity. Demonstrated ability to adapt priorities fluidly based on evolving business needs across a broad operational scope.

Strong experience building and maintaining PM documentation. Experience with metrics and data reporting, including presenting insights to senior stakeholders. Excellent written and verbal communication skills; confident facilitating cross-functional meetings and driving accountability.

Exceptional collaboration skills; this role requires daily partnership with a wide range of internal teams, IT partners, and external vendors; the ability to build strong working relationships across all levels is essential. Full training on Lx systems and tools will be provided; a willingness and ability to learn new platforms quickly. Work Style: Highly self-directed with strong ability to manage independently in a hybrid environment.

Proactive communicator who anticipates issues, escalates appropriately, and keeps stakeholders aligned. A natural collaborator who brings energy, structure, and follow-through to every team interaction. Comfortable operating across IT, commercial, digital, and cross-functional partner teams simultaneously.

Preferred Skills: Direct experience supporting commercial drug launches in a pharma / biotech setting. Prior Client experience or familiarity with Client commercial operations processes. Experience with specific therapy area launches (oncology, immunology, etc.).

Familiarity with UI / UX feedback cycles and digital platform lifecycle management. PMP certification or equivalent project management credential. SmartLaunch application experience.

Pay Rate: $75.83 - $80.43 / Hour If hired, you will enjoy the following ECLARO Benefits: 401k Retirement Savings Plan administered by Merrill Lynch Commuter Check Pretax Commuter Benefits Eligibility to purchase Medical, Dental & Vision Insurance through ECLARO If interested, you may contact: Paul Quibuyen Christian.Quibuyen@eclaro.com 646-695-2942 Paul Quibuyen | LinkedIn Equal Opportunity Employer: ECLARO values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status, in compliance with all applicable laws.