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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 ...

Kelly Services

Bioanalytical Scientist

Bridgewater, NJ · On-site

$27 - $38/hr

Scientist, Bioanalytical Kelly Outsourcing Consulting Group Kelly OCG, a managed solution provider ... Shows strong ownership of tasks and projects, ensuring compliance and reliability. * Provides ...

Kelly Services

Sr Technician, Bioanalytical

Somerset, NJ · On-site

$29 - $37/hr

Sr Technician, Bioanalytical Kelly Outsourcing Consulting Group Kelly OCG, a managed solution ... Shows strong ownership of tasks and projects, ensuring compliance and reliability. * Provides ...

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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 Jul 11, 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.

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 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.

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 July 2026, with employment types broken down into 1% Locum Tenens, 29% Internship, 11% Full Time, 55% Nights, and 4% Summer. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $96,560 per year, or $46.4 per hour.
Project Manager

Project Manager

ADARx Pharmaceuticals Inc.

San Diego, CA • On-site

$75K - $95K/yr

Full-time

Re-posted 3 days ago

Job description

The Project Manager is critical to advancing multiple pharmaceutical development programs simultaneously, ensuring cross-functional alignment across clinical operations and clinical development. This role drives timelines, coordinates internal and external stakeholders, mitigates risks, and helps accelerate program execution from development through clinical and commercial readiness.

Responsibilities

  • Develop and maintain clinical, nonclinical, and/or CMC timelines and project plans using inputs from the responsible subject matter experts from each function
  • Support Clinical Project Team Leads as needed with action item follow up, meeting minute publications, and other tasks pursuant to project / program deliverables
  • Manage external CROs via routine teleconferences and written correspondence to ensure that project deliverables are on time and within budget
  • Keep internal stakeholders appraised of project status and advise of risks to project timeline and actions needed to mitigate identified risks
  • QC and/or contribute to various reports, data, data tables, presentations, and/or documents for regulatory submissions (e.g., IND, IB) using advanced functions of MS Word, Excel and e-sub compliance software, as appropriate

On-Site Protocol:

Physical presence at the ADARx Pharmaceuticals worksite is required. The Company deems full critical engagement to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

Requirements / Qualifications

  • BS or MS in Toxicology, Bioanalysis or related field of study with 1-4+ years or relevant experience in the pharmaceutical industry
  • PMP certification is preferred
  • Must be highly organized, detail oriented, with the ability to multi-task and be flexible and adaptive in a fast-paced environment.
  • Excellent oral and written communication
  • Familiarity with MS Project, Smartsheet or other timeline / resource management tool
  • Hands-on experience in a GxP or regulated environment
  • Demonstrated understanding of various ICH guidance documents
  • Ability to travel on occasion for vendor audits, conferences, etc.

Required Key Attributes:

  • Must be able to work independently with supervision as needed.
  • Must be collaborative, work well with other Clinical Development team members in a matrix team environment.
  • Excellent written and verbal communication skills are essential for this role.
  • Strong organizational skills with attention to detail and accuracy.
  • Ability to maintain a high level of confidentiality and exercise discretion.
  • Adaptable / Flexible - willing and able to adjust to multiple demands and shifting priorities as well as an ability to meet day-to-day challenges.

ADARx Pharmaceuticals is an EEO employer committed to an exciting, diverse, and enriching work environment. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

Company Overview:

ADARx Pharmaceuticals, Inc., (the “Company” or “ADARx”) located in San Diego, is a late-clinical stage biotechnology company committed to turning cutting-edge science into life-saving therapeutics. ADARx has developed proprietary RNA targeting platforms and technology for silencing or editing target mRNA. ADARx has a growing pipeline of RNA targeting therapeutics for treating diseases across a range of therapeutic areas including genetic, cardiometabolic, complement-mediated diseases and central nervous system.