Contract Project Manager Medical Affairs

Clinical Dynamix; Bridgewater (MA); Hybrid; USD 89,544 - 117,096; Full time

Job summary

A leading pharmaceutical company is seeking a Contract Medical Affairs Project Manager to oversee the Osilodrostat Evidence Generation Plan. This hybrid role, based in Bridgewater, MA, requires strong project management skills and a background in pharmaceutical operations. Candidates should have at least 5 years of experience and a relevant Bachelor's degree, with an advanced degree preferred. Join this innovative team to drive impactful initiatives in medical affairs.

Qualifications

• 5+ years of experience in project management within pharmaceutical or biotech.
• Experience in evidence generation highly desirable.
• PMP or similar project management certification is a plus.

Responsibilities

• Lead project management of the Osilodrostat Evidence Generation Plan.
• Develop and manage project timelines, milestones, and deliverable tracking.
• Coordinate publication planning activities for visibility of data.

Skills

Project management

Communication skills

Stakeholder engagement

Financial tracking

Organizational skills

Education

Bachelor’s degree in life sciences, pharmacy, or public health

Advanced degree preferred

Tools

MS Project

Smartsheet

Asana

PowerPoint

Job description

Contract Medical Affairs Project Manager (Hybrid; 1 year contract)

Overview

The Medical Affairs (MA) Project Manager will oversee the operational execution of the Osilodrostat Evidence Generation Plan, ensuring timely delivery of studies, publications, and guideline updates that support brand growth and Company’s vision. This role will manage cross-functional and external partner coordination, ensuring scientific, compliance, and budgetary excellence across a portfolio of high-impact initiatives.

This range is provided by Clinical Dynamix. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$65.00/hr - $85.00/hr

Responsibilities

• Lead project management of the Osilodrostat Evidence Generation Plan, including RWE studies, ISSs, registries, and clinical trials.
• Develop and manage detailed project timelines, milestones, risk mitigation plans, and deliverable tracking across multiple workstreams.
• Partner with Clinical Development, Medical, HEOR, Regulatory, Legal, and Commercial teams to align evidence strategy with corporate objectives.
• Oversee vendor/partner performance, ensuring high-quality deliverables on time and within budget.
• Support compliant scientific exchange with internal and external stakeholders, ensuring proactive/reactive evidence dissemination by MSLs.
• Prepare and maintain project status dashboards, budget tracking, and progress updates for leadership review.
• Coordinate publication planning activities (abstracts, posters, manuscripts) to ensure visibility of data at major congresses.
• Ensure strict compliance with SOPs, GCP, and ethical/legal standards across all evidence generation activities.

Qualifications

• Bachelor’s degree in life sciences, pharmacy, public health, or related field required; advanced degree (MS, PharmD, MPH, PhD) preferred.
• 5+ years of experience in project management within pharmaceutical/biotech, CRO, or medical communications; direct experience in evidence generation highly desirable.
• Strong knowledge of real-world evidence, investigator-sponsored studies, and clinical trial operations.
• Demonstrated success in managing multiple tasks within multi-million-dollar, multi-year scientific programs.
• Proficiency in project management software (MS Project, Asana, Smartsheet), financial tracking, and PowerPoint.
• Excellent communication, organizational, stakeholder engagement, and presentation skills.
• PMP or similar project management certification a plus.

Knowledge and Skills

• Results-driven with the ability to manage complexity and competing priorities.
• Strategic thinker who can connect scientific objectives to execution.
• Strong collaboration and influencing skills across cross-functional teams.
• High attention to detail, compliance mindset, and operational rigor.

Location/Travel

• The location for this position is the Bridgewater, New Jersey office.
• Hybrid role; Tuesday/Wednesday/Thursday required on-site.
• The position may require some travel (<10%).

Seniority level

Associate

Employment type

Contract

Job function

Project Management

Industries

Pharmaceutical Manufacturing and Biotechnology Research