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Biotechnology Project Manager Jobs in Haddonfield, NJ

Braskem

Project & Construction Manager

Marcus Hook, PA · On-site

... in biotechnology and chemical catalysis. For more information, visit www.braskem.com/usa ... The Project Manager for the Marcus Hook site is responsible for end-to-end delivery of capital ...

New

INC Research

Senior Project Data Manager

Philadelphia, PA · On-site

$52.25 - $70.75/hr

... biotech and medical device industries. We do this across six continents, and we'll do it for you ... Acts as Project Leader on a stand alone contract ("project") for Data Management, to include: a ...

INC Research

Senior Project Data Manager

Philadelphia, PA · On-site

$52.25 - $70.75/hr

... biotech and medical device industries. We do this across six continents, and we'll do it for you ... Acts as Project Leader on a stand alone contract ("project") for Data Management, to include: a ...

DPS Group

Sr. Project Architect

Conshohocken, PA · On-site

$97K - $124K/yr

DPS seeks a person with a strong architectural background in biotech/biopharm and/or R&D laboratory design. The Senior Project Architect will report to the Architecture Department Manager. Key ...

KBR

Project Engineering Lead

Philadelphia, PA

Support the PMC Project Manager, while providing leadership, direction, and oversight to a ... Experience supporting pharmaceutical or biotechnology facilities. * Prior experience in an Owner ...

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Biotechnology Project Manager information

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How much do biotechnology project manager jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for biotechnology project manager in Haddonfield, NJ is $44.55, according to ZipRecruiter salary data. Most workers in this role earn between $38.65 and $48.85 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 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 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 job categories do people searching Biotechnology Project Manager jobs in Haddonfield, NJ look for?

The top searched job categories for Biotechnology Project Manager jobs in Haddonfield, NJ are:

What cities near Haddonfield, NJ are hiring for Biotechnology Project Manager jobs?

Cities near Haddonfield, NJ with the most Biotechnology Project Manager job openings:

Biotechnology Project Manager jobs near you
Infographic showing various Biotechnology Project Manager job openings in Haddonfield, NJ as of August 2026, with employment types broken down into 80% Full Time, 19% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $92,662 per year, or $44.5 per hour.

Associate Director, R&D Project Management

Biopharma Careers

King Of Prussia, PA • On-site

$170 - $210/hr

Other

Posted 2 days ago

New

Job description

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide.

Could you be our next Associate Director, Project Management? The job is in our King of Prussia, PA or Maidenhead UK office. This is a hybrid position and is onsite three days a week. You will report to TA Portfolio Delivery Lead.

Position Description:

Responsible for leading the successful operational delivery of global, cross functional R&D projects of strategic importance to CSL's product portfolio.

Main Responsibilities & Accountabilities:
  • Work closely with project leader to define strategy and operational tactics
  • Responsible for the preparation and management of project budgets, sensitivities, resources, project timelines, project scope and all other project documentation
  • Accountable for the accuracy and quality of reports to senior stakeholders
  • Lead cross functional development teams through tactical execution of project plans
  • Identify, manage and resolve project issues and mitigate risks
  • Ensure documentation of key team information, decisions, actions, modifications to scope, resources, timelines and milestones in project management systems is current.
  • Identify, evaluate the critical path, scenarios and challenge assumptions to increase robustness of project plans
  • Monitor performance vs. plan (budget and timeline)
  • Coordinate program updates to Sr. Management
  • Provide coaching and mentorship to more junior members of the R&D Global Project Management Department
Qualifications and Experience
  • Bachelor degree or equivalent in Science, Engineering, or a related field.
  • 10+ years' experience in the biotechnology or pharmaceutical industry
  • 5+ years' experience as project manager leading cross-functional project teams in a matrixed, global environment, in-depth knowledge in drug research, development and manufacturing processes
  • Demonstrated experience in delivering projects to meet business objectives on time, within budget and with quality.

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About CSL Behring

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.

To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/ .

Our Benefits

For more information on CSL benefits visit How CSL Supports Your Well-being | CSL .

You Belong at CSL

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging

Equal Opportunity Employer

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement .

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