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Biotechnology Project Manager Jobs in Hackensack, NJ

... biotechnology and healthcare companies in the agency setting ... Collaborates across team members to manage timelines, coordinate deliverables and bring key ...

Assure compliance with Medidata's standard project management methodologies and Medidata SOPs Qualifications : * Strong understanding of clinical research (pharma, device and/or biotech sectors) and ...

... manager forum, director forum, and AI fluency programs, to strengthen alignment, knowledge sharing ... Experience in pharmaceutical, biotech, or another highly regulated environment. * PhD degree with 7 ...

... manager forum, director forum, and AI fluency programs, to strengthen alignment, knowledge sharing ... Experience in pharmaceutical, biotech, or another highly regulated environment. * PhD degree with 7 ...

... biotechnology and healthcare companies in the agency setting ... Collaborates across team members to manage timelines, coordinate deliverables and bring key ...

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Biotechnology Project Manager information

See Hackensack, NJ salary details

$23

$50

$83

How much do biotechnology project manager jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for biotechnology project manager in Hackensack, NJ is $50.43, according to ZipRecruiter salary data. Most workers in this role earn between $43.80 and $55.34 per hour, depending on experience, location, and employer.

What does a biotechnology project manager do?

A Biotechnology Project Manager oversees and coordinates projects within the biotechnology industry, ensuring that research and development initiatives, product launches, or clinical trials are completed on time and within budget. They work with cross-functional teams, including scientists, engineers, and regulatory experts, to set project goals, manage resources, and monitor progress. Their responsibilities also include risk management, stakeholder communication, and ensuring compliance with industry regulations. This role is vital for driving innovation and bringing new biotech products or solutions to market efficiently.

What is the difference between Biotechnology Project Manager vs Research Scientist?

AspectBiotechnology Project ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Project Management certification often preferredMaster's or PhD in Biotechnology or related field
Work EnvironmentProject teams, corporate labs, industry settingsResearch labs, academic institutions, industry research divisions
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech startupsUniversities, research institutes, biotech companies

The main difference is that a Biotechnology Project Manager oversees project planning, coordination, and execution within biotech companies, focusing on timelines and budgets. In contrast, a Research Scientist conducts experiments and develops new biotech products or knowledge. Both roles require strong biotech credentials, but their daily tasks and focus areas differ significantly.

What are the key skills and qualifications needed to thrive as a biotechnology project manager, and why are they important?

To thrive as a Biotechnology Project Manager, you need a solid background in biological sciences or engineering, project management expertise, and often an advanced degree such as an MSc or PhD. Familiarity with tools like Microsoft Project, Gantt charts, regulatory compliance systems, and certifications such as PMP are commonly required. Strong leadership, communication, and problem-solving skills set exceptional candidates apart in managing cross-functional teams and complex timelines. These skills and qualities are essential to effectively coordinate scientific projects, ensure regulatory compliance, and deliver successful outcomes in a dynamic biotech environment.

What are some common challenges faced by biotechnology project managers in cross-functional team environments?

Biotechnology Project Managers often work with multidisciplinary teams composed of scientists, regulatory specialists, manufacturing experts, and business development professionals. One common challenge is ensuring clear communication and alignment across these diverse groups, especially when technical jargon or differing priorities create misunderstandings. Additionally, managing project timelines in a highly regulated environment, where unexpected trial results or compliance issues may cause delays, requires strong adaptive planning. Successful Biotechnology Project Managers foster collaboration by setting clear goals, conducting regular check-ins, and proactively addressing potential roadblocks.
What are popular job titles related to Biotechnology Project Manager jobs in Hackensack, NJ? For Biotechnology Project Manager jobs in Hackensack, NJ, the most frequently searched job titles are:
What job categories do people searching Biotechnology Project Manager jobs in Hackensack, NJ look for? The top searched job categories for Biotechnology Project Manager jobs in Hackensack, NJ are:
What cities near Hackensack, NJ are hiring for Biotechnology Project Manager jobs? Cities near Hackensack, NJ with the most Biotechnology Project Manager job openings:

Associate Director, Project Management - Value & Implementation (VIPM) (Hybrid)

MSD Malaysia

Rahway, NJ • On-site

$142.40 - $224.10/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago


Job description

Job Description

Global Project and Alliance Management (GPAM) is part of the Research and Development organization at our Company, which is also referred to as our Company's Research Laboratories. GPAM is comprised of Project Managers in Value & Implementation (which is this job), Development, and CMC; Discovery Portfolio Managers; Alliance Managers; Project Management Office (PMO); and Administrative Professionals.

Position Description/Summary: The GPAM Associate Director, Value & Implementation Project Manager (VIPM), is a core member of Value & Implementation (V&I) Team, partnering with team leaders to develop strategies and execute our Company's drug and vaccine V&I efforts to progress the R&D pipeline and realize its full potential. The Associate Director is expected to provide project management leadership and drive cross-functional teams with sufficient influence and mastery of project management to take on challenging assignments with minimal guidance. Projects could span any therapeutic areas in which our Company is actively engaged. In addition to project work, the Associate Director is expected to contribute to ongoing business process improvement and talent development in GPAM. This position may be based in either Rahway, NJ; Upper Gwynedd, PA; or Zurich, Switzerland.

Primary Responsibilities
  • Managing the Value and Implementation process, including projects of significant complexity
  • Driving cross-functional teams and leading by influence to develop comprehensive strategies and ensure successful execution
  • Act as enterprise leaders by guiding teams through the creation, approval, and execution of integrated project plans appropriate to the project’s phase of development and complexity
  • Integrating strategic and tactical input from disciplines (e.g., Medical Affairs, Outcomes Research, Market Access, Biostatistics and Research Decision Sciences, Commercial, and other areas) as applicable to the project
  • Building and maintaining project plans and critical project information in enterprise project management systems and databases
  • Using these tools to integrate activities across key team members, proactively identify risks, and ensure clear and effective communication with key team, management, and cross-departmental stakeholders
  • Leveraging relationships and networks to improve and enhance team dynamics; proactively identifying and removing obstacles to drive business results
  • Navigating our Company process and organizational norms to enable teams to understand corporate business requirements, thereby enabling decision-making
  • Leading key team meetings including creating thoughtful agendas, ensuring appropriate participation, contributing project management insights, and following up to ensure the team continues to make progress while holding others accountable
  • Participating in GPAM departmental initiatives and workstreams aimed at improving the way that we work and the way that we interact with one another and other departments
  • Improving business processes to find new efficiencies and connect people to the information that they need
  • Providing mentoring, coaching, and oversight to Specialist and Senior Specialist project managers working on common projects
  • Sharing lessons learned and best practices to impact the GPAM community positively
Required Education, Experience, and Skills
  • Bachelor’s degree required; concentration in a scientific or applied discipline preferred
  • Minimum of five (5) years of experience in project management or a related role required; in a pharmaceutical/biotech industry preferred
Preferred Experience and Skills
  • Advanced degree (e.g., MPH, MS, MBA, Ph.D., PharmD) preferred
  • Experience and knowledge of different components of value and implementation strongly preferred; including how the various functional areas contribute to a comprehensive strategy
  • Project management certification (PMP) and/or formal coursework/training in project management strongly preferred
Travel Requirements
  • 10%
Required Skills
  • Adaptability
  • Biostatistics
  • Business Processes
  • Business Process Improvements
  • Change Management
  • Clinical Research
  • Cross-functional Leadership
  • Drug Development
  • Multiple Therapeutic Areas
  • Outcomes Research
  • Process Optimization
  • Program Implementation
  • Project Human Resource Management
  • Project Management Information Systems (PMIS)
  • Project Planning
  • Publications Management
  • Regulatory Compliance
  • Risk Management
  • Sourcing and Procurement
  • Strategic Planning
  • Strategic Thinking
Preferred Skills
  • Implementation Management
  • Implementation Planning
  • Matrix Leadership
US and Puerto Rico Residents Only

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts

San Francisco Residents Only

We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only

We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Benefits
  • Medical
  • Dental
  • Vision healthcare and other insurance benefits (for employee and family)
  • Retirement benefits, including 401(k)
  • Paid holidays
  • Vacation
  • Compassionate and sick days
Salary Range

The salary range for this role is $142,400.00 - $224,100.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

Employment Details
  • Employee Status: Regular
  • Relocation: No relocation
  • VISA Sponsorship: No
  • Travel Requirements: 10%
  • Flexible Work Arrangements: Hybrid
  • Shift: Not Indicated
  • Valid Driving License: No
  • Hazardous Material(s): n/a
Job Posting End Date

Job Posting End Date: 08/6/2026

Company Overview

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

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