ZipRecruiter

Log In

1

Contractual Preclinical Study Monitor Jobs (NOW HIRING)

RPM ReSearch

Study Coordinator, Manager

Birmingham, AL · On-site

$80K - $110K/yr

... preclinical studies. You will play an instrumental role in optimizing workflows, monitoring financial impact, enhancing cross-functional processes, and elevating the quality of deliverables. This is ...

next page

Showing results 1-20

All JobsContractual Preclinical Study Monitor Jobs

Contractual Preclinical Study Monitor information

What cities are hiring for Contractual Preclinical Study Monitor jobs? Cities with the most Contractual Preclinical Study Monitor job openings:
What are the most commonly searched types of Preclinical Study Monitor jobs? The most popular types of Preclinical Study Monitor jobs are:
What states have the most Contractual Preclinical Study Monitor jobs? States with the most job openings for Contractual Preclinical Study Monitor jobs include:
Contractual Preclinical Study Monitor jobs near you
Infographic showing various Contractual Preclinical Study Monitor job openings in the United States as of July 2026, with employment types broken down into 89% Full Time, 9% Part Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution.

Associate Project Manager -Preclinical Studies

Pharmaron

Exton, PA • On-site

$50K - $55K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 7 days ago

Job description

Associate Project Manager -Preclinical Studies
Location
Exton, PA (onsite)
Salary Range: $50,000-55,000
About Pharmaron
Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.
We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit .
Job Summary
This is an excellent opportunity for an early-career professional with a life sciences background who enjoys working at the intersection of science, client service, and project coordination.
Are you looking to combine your scientific knowledge with project management in a collaborative drug discovery environment? We are seeking an Associate Project Manager with 1-2yrs' experience to support preclinical In Vivo Pharmacokinetics (PK) and Drug Metabolism and Pharmacokinetics (DMPK) studies. In this role, you'll partner with scientists, clients, and cross-functional teams to ensure studies are delivered on time, within budget, and to the highest quality standards.
What You'll Do
As an Associate Project Manager, you will oversee projects from quote generation through final study deliverables while serving as a key communication link between clients and internal teams.
Key responsibilities include:
  • Prepare scientifically accurate study quotes and budgets.
  • Develop and process change orders as project scope evolves.
  • Coordinate project timelines, milestones, and deliverables to ensure successful execution.
  • Maintain proactive communication with clients and internal stakeholders throughout each study.
  • Monitor project progress, identify risks, and help resolve issues before they impact timelines.
  • Support the in vivo PK team by assisting with scientific report drafting and documentation.
  • Coordinate resources, including personnel, equipment, laboratory space, and external vendors.
  • Manage multiple active projects simultaneously while maintaining exceptional attention to detail.
  • Maintain accurate project documentation and records across internal systems.
  • Participate in project meetings and contribute to continuous improvement initiatives.
  • Stay informed of industry trends, regulatory requirements, and drug development best practices.
  • Collaborate with Scientific, Executive, Legal, Accounting, Sales & Marketing, and Operations teams across multiple U.S. laboratory sites.

Qualifications
Required
  • Bachelor's degree in Pharmaceutical Sciences, Life Sciences, Chemistry, Pharmacology, or a related scientific discipline.
  • Minimum of one year of pharmaceutical, biotechnology, CRO, or related industry experience.
  • Experience with scientific writing or report preparation.
  • Strong written and verbal communication skills.
  • Excellent organizational, documentation, and proofreading abilities.
  • Ability to manage multiple priorities in a fast-paced, collaborative environment.
  • Strong problem-solving skills with exceptional attention to detail.

Preferred
  • Experience working within a Contract Research Organization (CRO).
  • Working knowledge of preclinical DMPK and bioanalysis.
  • Understanding of in vivo pharmacokinetics in rodents and large animal models.
  • Familiarity with LC-MS/MS bioanalysis.
  • Knowledge of pharmaceutical drug discovery and development processes.
  • Experience with project pricing, budgeting, client contracts, or scope management.

What Makes You Successful
You are someone who:
  • Enjoys collaborating with multidisciplinary teams.
  • Communicates effectively with clients and internal stakeholders.
  • Thrives in a dynamic, fast-paced environment.
  • Takes initiative and adapts quickly to changing priorities.
  • Is highly organized and committed to delivering quality work.
  • Can anticipate project challenges and develop practical solutions.

Work Environment
  • Full-time, on-site position.
  • Occasional travel to other U.S. laboratory locations.
  • Combination of office and laboratory work environments.
  • Ability to work at a computer for extended periods and occasionally within laboratory settings.

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
  • Insurance including Medical, Dental & Vision with significant employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance
  • 401k plan with generous employer match
  • Access to an Employee Assistance Program

How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
#LI-PR1

Apply