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Bioanalytical Project Manager Jobs in Edison, NJ

Senior Scientist, Analytical R&D

Rahway, NJ · On-site

$100K - $127K/yr

Lead and apply project management skills to analytical method validation and transfer activities ... Bioanalytical Analysis, Biochemical Assays, Bioprocess Engineering, Bioproducts, Cell-Based Assays ...

PK/PD Senior Scientist

Parsippany, NJ · On-site +1

$114K - $185K/yr

Collaborate with bioanalytical team to assess suitability of analytical assays and forecast ... project. * Present research results to scientific teams, management, and regulatory agencies.

... bioanalytical assays that are required for the GLP or CGLP studies. She/he may be involved in ... Strong project management skills. * Ability to articulate QA-GLP perspective and the status of QA ...

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Bioanalytical Project Manager information

See Edison, NJ salary details

$46.1K

$100K

$159.9K

How much do bioanalytical project manager jobs pay per year?

As of Jun 27, 2026, the average yearly pay for bioanalytical project manager in Edison, NJ is $99,964.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,600.00 and $117,000.00 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.

What are popular job titles related to Bioanalytical Project Manager jobs in Edison, NJ? For Bioanalytical Project Manager jobs in Edison, NJ, the most frequently searched job titles are:
What job categories do people searching Bioanalytical Project Manager jobs in Edison, NJ look for? The top searched job categories for Bioanalytical Project Manager jobs in Edison, NJ are:
What cities near Edison, NJ are hiring for Bioanalytical Project Manager jobs? Cities near Edison, NJ with the most Bioanalytical Project Manager job openings:
Infographic showing various Bioanalytical Project Manager job openings in Edison, NJ as of June 2026, with employment types broken down into 96% Full Time, 3% Part Time, and 1% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $99,964 per year, or $48.1 per hour.
Bioanalytical Principle Investigator-Biomarkers

Bioanalytical Principle Investigator-Biomarkers

Syneoshealth

Princeton, NJ • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 17 days ago


Syneos Health rating

8.5

Company rating: 8.5 out of 10

Based on 19 frontline employees who took The Breakroom Quiz

18th of 73 rated pharmaceutical


Job description

Bioanalytical Principle Investigator-Biomarkers

Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver - for one another, our customers, and, most importantly, for those in need.
Discover what your 25,000 future colleagues already know:
Why Syneos Health
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to building an inclusive culture - where you can authentically be yourself. Central to this is our purpose - Driven to Deliver - which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life.
We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

Plan, organize, manage and monitor their work unit's activities according to their field of expertise, the work plan, and the needs of the organization in order to achieve the expected results.

Collaborate on various critical activities such as workforce planning, hiring, provide input in performance management and daily monitoring of productivity; facilitate knowledge development and ensure the team's efficiency and mobilization.

Help to develop their work unit's performance indicator systems and the analysis of established objectives. Identify opportunities for improvement. Determine, as needed, the necessary actions to be taken in order to streamline efficiency.

Monitor and manage budgets of assigned projects and ensure adeherence and complete revenue recgnition. Perform budget follow-up for pertinent stakeholders and recommend actions in an effort to achieve the expected results.

Communicate the necessary information to ensure colleagues and the organization are aware of their team's work plan, policies, projects, processes, results, and actions.

Collaboration with partners in the Training team to ensure training is available for team members.

Represent their work units, both internally and externally, as to consultation and/or information and/or reference.

Advise internal/external clients of their division's particular areas of expertise by assessing needs, and by carrying out analysis and follow-ups.

Participate in regulatory agency inspections and client audits as well as the ensuing response process.

Project manager role:

Primary client liaison and point of contact for assigned sponsor projects. Receive and distribute information as appropriate from each of these sponsors. Keep the sponsors fully informed of timelines, project milestones and ensure timely communication on bioanalytical studies.

Support business development activities to grow and maintain new and existing clients.

Serve as the Principal Investigator for pre-clinical and bioanalytical studies.

Prepare, revise and/or approve all documentation related to the assigned projects.

Parnet with Business Development and the Cost Proposal team to prepare various quotes related to service requests made by clients.

Responsible for the technical and regulatory requirements of the bioanalytical study.

At times, may direct and participate in the development of new bioanalytical methods. Provide technical expertise to the laboratory staff.

Administrative responsibilities including a detailed, accurate short-term forecast of revenue (3 months) and a less detailed long-term forecast (6-9 months) Daily interaction with the scientific team and management to establish priorities of assignments.

Result analysis/reporting manager role:

Review audit reports and observations in order to maintain a high level of quality and consistency.

Ensure monitoring of corrective actions and preventive actions (CAPA).

Ensure the smooth functioning and quality of result analysis. Involve in problem solving and decision-making.

Involve in bioanalytical report writing and prioritization.

Ensure compliance and evaluate, identify and communicate the regulatory risks to senior management.

Participate in the harmonization of work methods between the different divisions/services as well as the different sites.

Participate in drafting/revising SOPs.

Optimize and ensure the implementation of their teams working procedures and techniques in order to improve quality.

Direct and guide archive management within the division.

Review data and results ahead of client / internal delivery to ensure data is in line with quality expectations.

Additional Qualifications

Experience in the management of technical and scientific staff.

Demonstrated leadership, line management, tactical and strategic thinking skills.

Extensive knowledge of GLP/EMA guidelines and other applicable regulatory requirement.

Must demonstrate good computer skills especially in the utilization of Microsoft Word and Excel.

Excellent communications, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade.

Experience within a client-service environment, either in a contract laboratory or within a core group at a pharmaceutical company. Demonstrate scientific problem solving skills.

At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.

Salary Range:

$79,800.00 - $139,600.00

The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role.

Get to know Syneos Health


Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information


Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.


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