1

Biopharma Project Manager Jobs (NOW HIRING)

Project Manager

Lake Zurich, IL · On-site

$110K - $120K/yr

Design and manage projects for all KPI & analytical reporting via Qlik (Power BI) steams and applications for the biopharma team and build a strong cross-functional relationship with commercial ...

Project Manager

Lake Zurich, IL · On-site

$110K - $120K/yr

Design and manage projects for all KPI & analytical reporting via Qlik (Power BI) steams and applications for the biopharma team and build a strong cross-functional relationship with commercial ...

Project Manager

Lake Zurich, IL · On-site

$110K - $120K/yr

Design and manage projects for all KPI & analytical reporting via Qlik (Power BI) steams and applications for the biopharma team and build a strong cross-functional relationship with commercial ...

Project Manager

Lake Zurich, IL · On-site

$110K - $120K/yr

Design and manage projects for all KPI & analytical reporting via Qlik (Power BI) steams and applications for the biopharma team and build a strong cross-functional relationship with commercial ...

The Global Project Manager (GPM) is critical to the successful conduct of Biopharmaceutical-sponsored clinical trials as a matrix leader of the core project team. The GPM is responsible for the ...

The Global Project Manager (GPM) is critical to the successful conduct of Biopharmaceutical-sponsored clinical trials as a matrix leader of the core project team. The GPM is responsible for the ...

CDMO Project Manager

Saint Louis, MO · On-site

$89K - $133K/yr

Louis, Missouri Your Role We are looking for a successful, true Project Manager for our Cherokee ... biopharmaceutical operations * Exceptional attention to detail with experience in meticulous ...

Position Summary We are seeking a seasoned Deputy Project Manager to help lead the construction of a large-scale biopharmaceutical manufacturing plant in Texas. In this critical leadership role, you ...

next page

Showing results 1-20

Biopharma Project Manager information

See salary details

$44.5K

$96.6K

$154.5K

How much do biopharma project manager jobs pay per year?

As of Sep 10, 2026, the average yearly pay for biopharma project manager in the United States is $96,560.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,000.00 and $113,000.00 per year, depending on experience, location, and employer.

What does a biopharma project manager do?

A Biopharma Project Manager oversees the planning, execution, and completion of projects within the biopharmaceutical industry. They coordinate cross-functional teams, manage timelines and budgets, and ensure that project goals align with regulatory requirements and company objectives. Their role is critical for bringing new drugs and therapies from development to market efficiently while maintaining compliance and quality standards.

What are some common challenges biopharma project managers face when coordinating cross-functional teams?

Biopharma Project Managers frequently encounter challenges in aligning the goals and timelines of diverse teams such as R&D, regulatory affairs, clinical operations, and manufacturing. These teams often have different priorities and work rhythms, which can create communication gaps or delays. Effective project managers proactively facilitate clear communication, set realistic expectations, and regularly update stakeholders to ensure everyone is moving toward shared project milestones. Building strong relationships and fostering a collaborative environment are crucial for overcoming these hurdles and driving projects to successful completion.

What are the key skills and qualifications needed to thrive as a biopharma project manager, and why are they important?

To thrive as a Biopharma Project Manager, you need a solid background in life sciences or pharmaceutical development, project management expertise, and often a relevant degree such as a PMP certification or advanced scientific degree. Familiarity with project management tools (like MS Project or Smartsheet), regulatory systems (such as FDA or EMA guidelines), and budgeting software is typically required. Excellent communication, leadership, and problem-solving skills are crucial for managing cross-functional teams and ensuring project milestones are met. These competencies are vital for delivering complex projects on time and within budget, while ensuring compliance and fostering innovation in a highly regulated industry.

What is the difference between Biopharma Project Manager vs Clinical Research Coordinator?

AspectBiopharma Project ManagerClinical Research Coordinator
CredentialsTypically requires a bachelor’s degree in life sciences, project management certification (e.g., PMP)Usually holds a bachelor’s degree in health sciences or related field; certifications like CCRP are common
Work EnvironmentManages projects across departments in biotech or pharmaceutical companiesWorks directly on clinical trial sites, coordinating patient recruitment and data collection
Employer & IndustryBiotech, pharmaceutical companies, contract research organizationsHospitals, clinical research organizations, academic medical centers

The Biopharma Project Manager oversees the planning and execution of biopharmaceutical projects, focusing on timelines, budgets, and team coordination. In contrast, the Clinical Research Coordinator handles the day-to-day operations of clinical trials, ensuring compliance and data accuracy. Both roles require knowledge of clinical processes but differ in scope and responsibilities.

What are popular job titles related to Biopharma Project Manager jobs?

For Biopharma Project Manager jobs, the most frequently searched job titles are:

Infographic showing various Biopharma Project Manager job openings in the United States as of September 2026, with employment types broken down into 86% Full Time, 13% Part Time, and 1% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $96,560 per year, or $46.4 per hour.

Project Manager

Lake Zurich, IL • On-site

$110K - $120K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 14 days ago


Job description

Job SummaryThe individual should have a good working knowledge and understanding of the biosimilars market and support complex projects charged with successful completion of tasks required to support the biopharma division. Creates integrated project plans and schedules, drives identification and mitigation of project risks, performs ongoing project monitoring and ensures adequate dissemination of information to project stakeholders. Responsible for managing multiple projects simultaneously in a fast-paced start-up environment. The incumbent is expected to work with cross-functional teams across Global and US Marketing, Market Access, Sales, Medical Affairs, Finance, Commercial Excellence, and more.
Salary Range: $110,000 - $120,000 per year
Position is eligible to participate in a bonus plan with a target of 10% of the base salary. Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities. Our benefits and programs are comprehensive and thoughtfully crafted to ensure our colleagues live healthy lives and have support when it matters most.Responsibilities
  • Manage all aspects of any assigned strategic development project(s); inclusive of direct shipping contracts for strategic customers and reporting of all financial benefits and KPIs related to these project(s).
  • Design and manage projects for all KPI & analytical reporting via Qlik (Power BI) steams and applications for the biopharma team and build a strong cross-functional relationship with commercial excellence business partners to help prioritize the needs of the biopharma.
  • Manage complex projects related to both medical and pharmacy benefit dispense biosimilars across various therapeutic areas including immunology, oncology, etc.
  • Assist and drive the project and workstream to develop an innovative 340B strategy related to contract pharmacies that includes revamping of system transactions withing Model N. Document the government regulation and policies that help define and shape the innovative 340B policy. Work cross functionally with 3rd parties and build strong relationships as needed to assist in this project.
  • Define the scope of work for each new project, clearly identify tasks and responsibilities for all project team members and establish target completion dates for key project milestones. Interface with department managers and senior management to facilitate allocation and prioritization of resources necessary to achieve key project milestones within established timelines. Administer the time tracking tool to ensure proper capacity planning and actuals reporting of project resources for assigned projects.
  • Maintain and routinely update biopharma leadership and necessary teams of status and KPIs of ongoing projects or strategic development opportunities.
  • Identify and resolve emerging risks / issues that may impact project, department or regional goals. Recognize potential threats to project success and elevate issues to department management when necessary.
  • Conduct lessons learned and project close-out sessions to obtain information that can be used to improve future projects. Contribute & develop biopharma project management knowledgebase through development and revision of project management tools and templates.
  • Manage project budgets and participate in quarterly forecasting and budgeting exercises.
Requirements
  • Bachelor's degree in a finance/accounting field required. MBA preferred.

  • 5+ years of pharmaceutical work experience with 3+ years managing a portfolio of projects in the pharmaceutical industry.

  • Strong ability to think analytically, execute to a goal/vision, influence, problem solve, and impact/drive change in a heavily matrixed global environment.

  • Demonstrates independence and must be self-driven.

  • Work with cross functional teams.

  • Excellent communication and presentation skills, both oral and written.

  • Must be able to think innovatively and strategically and have a desire for learning.

  • Proficient in Microsoft Excel, Word, Project, Power Point, SAP, Qlik, and TM1.

  • Ability to travel, including international travel.

  • The Company's primary business language is English. The successful candidate must be able to effectively speak, read, write, and understand English to perform the essential functions of the position, including independently understanding policies, procedures, training materials, and workplace communications written in English due to our heavily regulated work environment.

Additional Information

We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability,401K with company contribution, andwellness program.

Please note that joining our team does not create a guaranteed or permanent employment arrangement. All employment is atwill, meaning both the employee and Fresenius Kabi have the right to end the employment relationship at any time, in accordance with applicable federal and state laws.

Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.