ZipRecruiter

Log In

1

Preclinical Project Manager Jobs in Raritan, NJ (NOW HIRING)

previous pagenext page

Showing results 21-40

All JobsPreclinical Project JobsPreclinical Project Manager JobsPreclinical Project Manager Jobs in Raritan, NJ

Preclinical Project Manager information

See Raritan, NJ salary details

$39.4K

$105.2K

$165.9K

How much do preclinical project manager jobs pay per year?

As of Sep 9, 2026, the average yearly pay for preclinical project manager in Raritan, NJ is $105,150.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,400.00 and $126,000.00 per year, depending on experience, location, and employer.

What does a preclinical project manager do?

A Preclinical Project Manager oversees the planning, coordination, and execution of preclinical research projects that typically involve laboratory and animal studies before clinical trials in humans can begin. They work closely with scientists, regulatory teams, and stakeholders to ensure that studies are conducted according to protocols, timelines, and regulatory requirements. Their responsibilities include managing budgets, resources, and communication among various teams to advance drug candidates or medical devices through the early stages of development. Effective Preclinical Project Managers help ensure that projects meet scientific and business objectives, and that all data generated is reliable and compliant with industry standards.

How does a preclinical project manager typically coordinate with cross-functional teams during a drug development project?

A Preclinical Project Manager works closely with scientists, regulatory affairs, toxicology, and external vendors to ensure all preclinical studies are executed on time and within budget. They facilitate regular meetings to align project milestones, address challenges, and manage documentation for compliance. Effective communication and proactive issue resolution are key, as the role often requires balancing the needs of diverse stakeholders while keeping the overall project timeline on track.

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

To thrive as a Preclinical Project Manager, you need a solid background in life sciences or pharmaceutical research, often with an advanced degree and experience managing preclinical studies. Familiarity with project management tools, regulatory guidelines (such as GLP), and software like Microsoft Project or similar platforms is typically required. Strong organizational, leadership, and communication skills are vital for coordinating cross-functional teams and ensuring project timelines are met. These skills and qualifications are crucial for efficiently advancing drug candidates through preclinical development while ensuring compliance and project success.

What job categories do people searching Preclinical Project Manager jobs in Raritan, NJ look for?

The top searched job categories for Preclinical Project Manager jobs in Raritan, NJ are:

What cities near Raritan, NJ are hiring for Preclinical Project Manager jobs?

Cities near Raritan, NJ with the most Preclinical Project Manager job openings:

Preclinical Project Manager jobs near you
Infographic showing various Preclinical Project Manager job openings in Raritan, NJ as of August 2026, with employment types broken down into 94% Full Time, and 6% Contract. Highlights an 84% In-person, and 16% Remote job distribution, with an average salary of $105,150 per year, or $50.6 per hour.

Distinguished Scientist, Safety Assessment Project Expert

Morristown, NJ • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

$200 - $250/hr

Other

Posted 10 days ago

Job description

Main Responsibilities
  • Serve as a Preclinical Safety Project Team Member on multi-functional R&D project teams (small molecules, biotherapeutics, oligonucleotides, and other modalities); develop and implement toxicology and safety pharmacology strategies.
  • Support nonclinical safety activities across early-/late-stage development and Life Cycle Management/marketed products.
  • Write nonclinical summaries for Investigator Brochures, INDs, CTAs, NDAs/BLAs, Pediatric Investigation Plans, Scientific Advice, and other regulatory documents; review internal/external reports to provide scientific preclinical safety perspective.
  • Ensure high scientific standards in conducting and reporting nonclinical safety and investigative toxicology studies; provide leadership with experience interpreting reproductive and developmental toxicity (preferred).
  • Provide internal expertise for global nonclinical safety issues for committees/expert groups; prepare publications and presentations.
  • Participate in special projects/inter-industry working groups.
  • Provide scientific input on R&D study design and analysis, including in-licensing opportunity evaluations.
Qualifications
  • PhD or DVM in biochemistry, toxicology, pharmacology, biology, physiology, pathology, statistics, or related field; 12+ years pharmaceutical industry experience.
  • Demonstrated knowledge of GLP and ICH policies and regulatory nonclinical testing requirements.
  • Demonstrated experience preparing and submitting IND and CTD submissions.
Minimum/Preferred Skills
  • Experience as a GLP Study Director.
  • Experience with ophthalmology toxicity study conduct and interpretation.
  • Certification by the American Board of Toxicology.
  • Excellent presentation and writing skills.
  • English.
Benefits
  • At least 14 weeks’ gender-neutral parental leave.
#J-18808-Ljbffr

Apply