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Bioanalytical Project Manager Jobs (NOW HIRING)

ADARx Pharmaceuticals Inc.

Project Manager

San Diego, CA · On-site

$75K - $95K/yr

The Project Manager is critical to advancing multiple pharmaceutical development programs ... Requirements / Qualifications * BS or MS in Toxicology, Bioanalysis or related field of study with ...

MSD

Senior Bioanalytical Associate

Gaithersburg, MD · On-site

$67K - $101K/yr

... bioanalytical projects. DUTIES AND RESPONSIBILITIES: * Perform sample analysis with minimal ... Proficiency in MS Office suite; familiarity with electronic file management using SharePoint (end ...

Syneoshealth

OR

Clinical Project Manager II - Biomarker Study Management Experience required (Sponsor Dedicated ... Oversee biomarker and bioanalytical activities across Sponsor and Collaborative programs * Serve as ...

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Bioanalytical Project Manager information

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$44.5K

$96.6K

$154.5K

How much do bioanalytical project manager jobs pay per year?

As of Jun 20, 2026, the average yearly pay for bioanalytical 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.

Can I make 100k as a project manager?

Bioanalytical Project Managers can earn $100,000 or more annually, especially with experience, advanced certifications, and working in the pharmaceutical or biotech industries. Salaries vary based on location, company size, and project scope, with senior roles and those managing larger teams typically earning higher compensation.

What does a Bioanalytical Project Manager do?

A Bioanalytical Project Manager oversees and coordinates bioanalytical studies, ensuring that projects are completed on time, within budget, and according to regulatory standards. They act as the main point of contact between clients, laboratory teams, and regulatory agencies, managing study timelines, resources, and data quality. Their responsibilities include planning project activities, monitoring progress, troubleshooting issues, and reporting results to stakeholders. They play a critical role in drug development by ensuring that bioanalytical testing meets scientific and compliance requirements.

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

To thrive as a Bioanalytical Project Manager, you need a strong background in bioanalysis, project management experience, and typically a degree in life sciences or a related field. Familiarity with laboratory information management systems (LIMS), regulatory guidelines (such as GLP/GCP), and project management tools like MS Project is essential. Excellent communication, leadership, and organizational skills help manage cross-functional teams and client expectations. These skills ensure the successful planning, execution, and delivery of complex bioanalytical projects within regulatory and timeline constraints.

What is the highest paying project manager job?

In the field of bioanalytical project management, senior roles such as Director of Project Management or Program Manager typically offer the highest salaries, often exceeding $120,000 annually. These positions require extensive experience, leadership skills, and often involve managing multiple projects or teams in a regulated environment.

What is the job description of a bioanalyst?

A bioanalytical project manager oversees the planning, execution, and validation of bioanalytical assays used in drug development and clinical trials. They coordinate laboratory activities, ensure compliance with regulatory standards, and manage timelines and budgets, often requiring knowledge of techniques like LC-MS/MS and relevant certifications. Strong project management and scientific expertise are essential for success in this role.

What are some common challenges faced by Bioanalytical Project Managers, and how can they be addressed?

Bioanalytical Project Managers often face challenges coordinating timelines across multiple stakeholders, such as laboratory teams, clients, and regulatory bodies. Managing shifting project priorities and ensuring data integrity under tight deadlines can also be demanding. To address these challenges, effective communication, proactive risk management, and strong organizational skills are essential. Regular status meetings, clear documentation, and building strong relationships with both internal and external partners help keep projects on track and ensure compliance with regulatory standards.

Are project managers still in demand?

Bioanalytical Project Managers are in demand due to the growth of the biotech and pharmaceutical industries, which require skilled professionals to oversee complex research projects. Strong project management skills, familiarity with regulatory requirements, and experience with laboratory tools increase employability in this field.

What is the difference between Bioanalytical Project Manager vs Bioanalytical Scientist?

AspectBioanalytical Project ManagerBioanalytical Scientist
CredentialsBachelor's or Master's in Life Sciences, PMP often preferredDegree in Biology, Chemistry, or related field; PhD or Master's common
Work EnvironmentProject teams, client meetings, coordination rolesLaboratory research, data analysis, method development
Employer & Industry UsagePharmaceutical, biotech companies, CROsResearch labs, pharmaceutical companies, CROs

The Bioanalytical Project Manager oversees project timelines, budgets, and client communication, ensuring successful completion. In contrast, the Bioanalytical Scientist focuses on experimental design, data collection, and method development. Both roles are essential in the bioanalytical industry but differ in responsibilities and daily tasks.

More about Bioanalytical Project Manager jobs
What cities are hiring for Bioanalytical Project Manager jobs? Cities with the most Bioanalytical Project Manager job openings:
What states have the most Bioanalytical Project Manager jobs? States with the most job openings for Bioanalytical Project Manager jobs include:
What job categories do people searching Bioanalytical Project Manager jobs look for? The top searched job categories for Bioanalytical Project Manager jobs are:
Bioanalytical Project Manager jobs near you
Infographic showing various Bioanalytical Project Manager job openings in the United States as of June 2026, with employment types broken down into 94% Full Time, and 6% Contract. Highlights an 96% In-person, 2% Hybrid, and 2% Remote job distribution, with an average salary of $96,560 per year, or $46.4 per hour.
Manager, Biomarkers and Bioanalytical Operations

Manager, Biomarkers and Bioanalytical Operations

Biogen

San Francisco, CA • On-site

$122K - $163K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago

Biogen rating

9.2

Company rating: 9.2 out of 10

Based on 18 frontline employees who took The Breakroom Quiz

3rd of 71 rated pharmaceutical

Job description

About This Role:
The Biomarker and Bioanalytical Operations Study Manager leads PK, ADA, and biomarker execution across clinical studies, partnering with study teams and CROs to deliver high-quality data on time. This role is critical to achieving key study endpoints and advancing programs through drug development and reports to the Head of Biomarker and Bioanalytical Operations.
What You'll Do
  • Serve as the primary Biomarker and Bioanalytical Operations lead for internal teams and external partners across Phase 1-4 studies

  • Lead end-to-end operational execution of biomarker and bioanalytical activities, including sample collection, processing, shipment, testing, storage, and data delivery

  • Implement clinical biomarker and bioanalytical strategies for early- and late-stage programs

  • Provide operational and sample management expertise to Study Management Teams (SMTs) and Biomarker Sub-Teams (BMSTs)

  • Ensure compliant, high-quality biomarker and bioanalytical sample collection aligned with protocols, ICFs, ethical standards, and regulations

  • Oversee CROs, central labs, and specialty vendors; manage performance, timelines, quality, contracts, and deliverables

  • Review and contribute operational input to protocols, CRFs, ICFs, proposals, budgets, study plans, and contracts

  • Develop study-specific biomarker and bioanalytical sample collection, handling, analysis, transport, and storage strategies

  • Partner cross-functionally (Clinical Biomarker, Clinical Pharmacology, Clinical Operations, Data Management, Business Operations & Contracts Partner) to enable efficient execution of the study

  • Define data collection, transfer, and reconciliation requirements with data management, bioanalytical leads, and vendors

  • Identify operational risks, implement mitigation plans, and support interim and final biomarker and bioanalytical reporting

  • Lead operational meetings, RFPs, vendor selection, and process improvement initiatives

  • Maintain biomarker operations systems and documentation; represent on cross-functional teams

  • Operate independently with general supervision; support investigator meetings and internal/external presentations as needed

Who You Are
You excel in fast-paced clinical development environments dedicated to advancing new therapies to patients. Your expertise in scientific operations, GCLP, and CRO management enables effective collaboration across internal teams and external laboratory partners.
Required Skills
Minimum Education & Experience
  • Advanced degree (PharmD or PhD) with 2+ years of relevant industry experience; MA or MS with 6+ years; or BA/BS or RN with 8+ years of comparable clinical, life sciences, or similar industry experience.

  • Good knowledge of phase I-IV clinical study operations as it pertains to specialty testing (PK, ADA, Biomarkers)

  • Experience working with contracted central labs and biomarker/bioanalytical testing labs including sample management, data management, testing requirements and timelines

  • Experience reviewing clinical protocols, ICFs, SOW, and contracts

  • Experience obtaining contracts and an understanding of Master Agreements and associated contracts

  • Experience working within GCP, GLP, & GCLP guidelines

  • Must be very organized and have the ability to manage multiple projects at a time

Preferred Skills
  • Demonstrated ownership of operational execution and accountability for outcomes

  • Proven ability to manage CROs and external vendors effectively

  • Solid understanding of clinical trial conduct and the drug development process

  • Strong cross-functional collaboration and stakeholder partnership skills

  • Clear, confident verbal and written communication

  • Proactive approach to identifying and managing operational risks

  • Strong organizational and prioritization skills

  • Continuous improvement mindset with a focus on optimizing processes and efficiency

This role involves minimal travel, typically under 10%.
Job Level: Management
Additional Information
The base compensation range for this role is: $122,000.00-$163,000.00
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees' and their families physical, financial, emotional, and social well-being; including, but not limited to:
  • Medical, Dental, Vision, & Life insurances
  • Fitness & Wellness programs including a fitness reimbursement
  • Short- and Long-Term Disability insurance
  • A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
  • Up to 12 company paid holidays + 3 paid days off for Personal Significance
  • 80 hours of sick time per calendar year
  • Paid Maternity and Parental Leave benefit
  • 401(k) program participation with company matched contributions
  • Employee stock purchase plan
  • Tuition reimbursement of up to $10,000 per calendar year
  • Employee Resource Groups participation

Why Biogen?
We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about Biogen.
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

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About Biogen

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At Biogen, our mission is clear - we are pioneers in neuroscience. Biogen discovers, develops, and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases. Together, our employees create, commercialize, and manufacture transformative therapies for our patient population.

Industry

Scientific research and development services

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

1978

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