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Bioanalytical Project Manager Jobs in Frederick, MD

Perform comprehensive quality review of bioanalytical assay data for accuracy, completeness, data ... Experience with project management tools such as Smartsheet preferred. * Ability to work ...

Perform comprehensive quality review of bioanalytical assay data for accuracy, completeness, data ... Experience with project management tools such as Smartsheet preferred. * Ability to work ...

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Bioanalytical Project Manager information

See Frederick, MD salary details

$44.2K

$96K

$153.6K

How much do bioanalytical project manager jobs pay per year?

As of Aug 21, 2026, the average yearly pay for bioanalytical project manager in Frederick, MD is $96,007.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,600.00 and $112,400.00 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?

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.

What are popular job titles related to Bioanalytical Project Manager jobs in Frederick, MD?

For Bioanalytical Project Manager jobs in Frederick, MD, the most frequently searched job titles are:

What job categories do people searching Bioanalytical Project Manager jobs in Frederick, MD look for?

The top searched job categories for Bioanalytical Project Manager jobs in Frederick, MD are:

What cities near Frederick, MD are hiring for Bioanalytical Project Manager jobs?

Cities near Frederick, MD with the most Bioanalytical Project Manager job openings:

Infographic showing various Bioanalytical Project Manager job openings in Frederick, MD as of August 2026, with employment types broken down into 83% Full Time, 16% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $96,007 per year, or $46.2 per hour.

Senior Study Coordinator

Meso Scale Discovery

Gaithersburg, MD • On-site

$67K - $101K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago


Job description

POSITION SUMMARY:

The Senior Study Coordinator (SC) provides support to the Bioanalytical Laboratory (BAL) staff for sample testing studies, including those performed under applicable elements of Good Laboratory Practices (GLP) and Good Clinical Laboratory Practices (GCLP), with minimal supervision. This includes, but is not limited to, project related support by creating study-specific documentation, assisting the Bioanalytical Principal Investigators (BPIs) in tracking project timelines and deliverables, and performing Quality Control review of study data. The Senior SC works closely with the BPIs to support the execution of BAL studies.

DUTIES AND RESPONSIBILITIES: 

• Independently drafts protocols, sample analysis plans (SAPs), protocol and SAP amendments, bioanalytical reports, and study schedules, using proposal outline or client-supplied information

• Reviews study records and reports for compliance against protocol, Standard Operating Procedures (SOPs), and GLP/GCLP requirements, as applicable

• Serves as a contact in communication and interaction with other departments and clients on project timelines and deliverables

• Participates in pre-initiation and other study related meetings as required

• Performs Quality Control review of study data and independently works with BPIs to resolve any identified issues

• Manages study documentation for multiple concurrent, moderate to high complexity projects

• Assists BPIs in analyzing and evaluating data for reports and managing data transfers to clients as requested

• Works closely with the data management team to create mock reports and test data transfers and report results to client

• Maintains well-documented, organized, and up-to-date study files including study schedule, protocol, and correspondence, as applicable

• Prepare study files for Archiving at the conclusion of the study

• Assists BPI in monitoring study phases, including updating and maintaining project tracking systems as appropriate

• Adheres to applicable principles of GLP and GCLP

EXPERIENCE AND QUALIFICATIONS:

• Bachelor’s degree in biology, chemistry, or other related scientific discipline, or equivalent work experience required

o Master’s degree is preferred

• Minimum of 2 years of experience in biological sample testing or reagent/assay development is required; experience in a clinical testing laboratory or contract research organization is highly preferred

• Experience in customer-facing, technical support, and/or consultative roles preferred

• Training in and experience with GLP and/or GCLP is preferred

KNOWLEDGE, SKILLS AND ABILITIES:

• Strong scientific fundamentals and analytical background

• Understanding of ligand-binding assays

• Excellent communication skills with the ability to organize, present, and articulate ideas both verbally and in writing

• A professional presence and strong interpersonal skills for interacting in a courteous, timely, and diplomatic manner with all levels of employees as well as external clients/customers

• Ability to receive, understand, and follow verbal and written directions

• Ability to communicate/delegate tasks/projects in a clear, concise manner that is easily understandable to all levels of support

• Excellent organizational skills with the ability to prioritize workload and meet deadlines with an appropriate sense of urgency

• Proficiency in MS Office suite; familiarity with electronic file management using SharePoint Ability to multi-task and work productively in a demanding environment with changing priorities

• Attention to detail with demonstrated commitment to excellence and performance

PHYSICAL DEMANDS: 

• This position requires the ability to communicate and exchange information, utilize equipment necessary to perform the job, and move about the office.

WORK ENVIRONMENT:

• This position is performed in a traditional office environment with periodic requirements to work with laboratory personnel in their designated work areas. 

COMPENSATION SUMMARY:

The annual base salary for this position ranges from $67,900 to $101,000. This salary range represents a general guideline as MSD considers other factors when presenting an offer of employment, such as scope and responsibilities of the position, external market factors, and the candidate’s knowledge, skills, abilities, education and experience. Employees may qualify for a discretionary or non-discretionary bonus in addition to their base salary. These annual bonuses are intended to recognize individual performance and enable employees to benefit from the Company's overall success.

BENEFITS SUMMARY:

At MSD, we offer a comprehensive benefits package to support our employees' well-being and financial security. In addition to competitive salaries, our benefits include medical, dental, and vision coverage, along with prescription benefits. We provide a 401(k) plan with company matching, flexible spending accounts, and company-paid short- and long-term disability insurance as well as group life and accidental death and dismemberment insurance. Our offerings also encompass paid vacation, paid sick leave, paid holidays, and paid parental leave, along with an employee assistance program. Additional voluntary perks include a fitness club membership contribution, pet insurance, identity theft protection, home and auto insurance discounts, and optional supplemental life insurance.

EEO/AA STATEMENT:

MSD is an Equal Opportunity/Affirmative Action Employer. We are committed to fostering a diverse and inclusive workplace where all individuals are treated with respect and dignity. We welcome applications from all qualified candidates, making employment decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, genetic information, marital status, national origin, age, protected veteran status, pregnancy, disability status, or any other protected characteristic. For our full EEO/AA and Pay Transparency statement, please click on the following link: https://www.mesoscale.com/en/our_company/careers/equal_employment_opportunity_statement. 

Meso Scale Diagnostics uses E-Verify to validate the work eligibility of candidates.