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Bioanalytical Project Manager Jobs in California

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 ...

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Bioanalytical Project Manager information

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.

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Bioanalytical Project Manager jobs near you
Infographic showing various Bioanalytical Project Manager job openings in California as of June 2026, with employment types broken down into 93% Full Time, 5% Part Time, 1% Temporary, and 1% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution.
TEMP - Sr. Scientist, Bioanalytical Outsourcing

TEMP - Sr. Scientist, Bioanalytical Outsourcing

Neurocrine Biosciences, Inc.

San Diego, CA • On-site

$97K - $132K/yr

Full-time

Posted 29 days ago

Job description

Who We Are:
Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in patients with Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X, Facebook and YouTube. (*in collaboration with AbbVie)
About the Role:
Responsible for all aspects of bioanalytical method development, validation and sample analysis at contract research organizations (CRO) according to project-relevant regulatory requirements and industry standards. Working with Preclinical Operations establish contracts and work orders for bioanalytical projects. Work with Clinical Pharmacology and Clinical Operations to plan and track bioanalytical method development, validation and sample analysis to support study initiation, execution and reporting. Ensure CROs capture and deliver on important expectations and agreed-to tasks in support of Neurocrine's clinical development programs.
Your Contributions (include, but are not limited to):
  • Oversee all aspects of bioanalytical method development, validation and sample analysis at contract research organizations (CRO) according to project-relevant regulatory requirements and industry standards for small and large molecule development
  • Work with R&D Operations and legal departments to establish contracts and work orders for bioanalytical projects
  • Oversee sample transfer and tracking from clinical sites or central lab to bioanalytical CROs
  • Ensure CROs are provided with requisite supplies and information to conduct sample analysis, including provision of reference and internal standards, CoA recertification, and statement of work completion
  • Plan and track critical reagent preparation, bioanalytical method development, validation and sample analysis activities to meet data requirements according to study protocols and timelines
  • Review bioanalytical validation plans, protocols and bioanalytical data to ensure alignment with current regulatory requirements
  • Attend regular meetings with CROs to facilitate updates. Capture important expectations and agreed to tasks in post-meeting minutes and share minutes with CROs and hold them accountable
  • Provide routine status updates to NBI Clinical, Clinical Pharmacology, QA, Accounting and Data Sciences colleagues
  • Review data transfer protocols, ensure proper data format, investigate data discrepancies and support data consolidation
  • Presents data and recommendations to internal and external stake holders
  • Other tasks as assigned

Requirements:
  • BS in Pharmacokinetics, Pharmaceutical Sciences, clinical pharmacology, or a related scientific discipline and 4+ years of experience in clinical-stage pharmaceutical development OR
  • MS in Pharmacokinetics, Pharmaceutical Sciences, clinical pharmacology, or a related scientific discipline and 3+ years of similar experience noted above OR
  • PhD in Pharmacokinetics, Pharmaceutical Sciences, clinical pharmacology, or a related scientific discipline and some relevant experience as noted above
  • Hands-on experience with the development, validation and troubleshooting of the bioanalytical methods and clinical sample analysis for small and large molecules
  • Knowledgeable on current relevant regulatory guidance / regulations (ICHM10)
  • Demonstrates solid level of understanding project / group goals and methods
  • Consistently recognizes anomalous and inconsistent results and interprets experimental outcomes
  • Able to explain the process behind the data and implications of the results
  • Strong knowledge of one or more scientific disciplines, becoming expert in one discipline
  • Strong knowledge of scientific principles, methods and techniques
  • Strong knowledge and demonstrated ability working with a variety of laboratory equipment/tools
  • Detail oriented yet can see broader picture of scientific impact on team
  • Excellent computer skills
  • Ability to meet multiple deadlines, with a high degree of accuracy and efficiency
  • Strong project management skill
  • Excellent problem-solving and analytical thinking skills
  • Strong written, presentation, and verbal communication skills
  • Proactive, innovative, with good problem-solving skills
  • Ability to work as part of a team; may train lower levels

The pay you should reasonably expect to receive is $53.27 - $77.21 per hour. Decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills.
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Neurocrine Biosciences is an EEO/Disability/Vets employer.
We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don't line up to exactly what we have outlined in the job description.

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