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Preclinical Project Manager Jobs in Ohio (NOW HIRING)

... preclinical) curriculum, including curriculum integration coordination, coordination of WrightQ ... project management, instructional design, or a related field OR an Associate's degree and five ...

GMP Senior Scientist

Columbus, OH ยท On-site

$70 - $95/hr

... ADC) for preclinical non-cGMP activities. Our Values are founded in our origin story. The name ... Excellent communication, organization, and project management skills with the ability to manage ...

$102 - $116/hr

Independently identify and lead translational research projects arising from clinical and biomarker ... management. * Contribute to budget planning and forecasting for assigned biomarker and ...

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Preclinical Project Manager information

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 are popular job titles related to Preclinical Project Manager jobs in Ohio?

For Preclinical Project Manager jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Preclinical Project Manager jobs in Ohio look for?

The top searched job categories for Preclinical Project Manager jobs in Ohio are:

What cities in Ohio are hiring for Preclinical Project Manager jobs?

Cities in Ohio with the most Preclinical Project Manager job openings:

Infographic showing various Preclinical Project Manager job openings in Ohio 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.

Principal Scientist, Preclinical Surgeon

6045-Ethicon Inc. Legal Entity

Cincinnati, OH โ€ข On-site

$100 - $130/hr

Other

Re-posted 15 days ago


Job description

Principal Scientist, Nonclinical Surgery โ€“ Cincinnati, OH

Functioning as a primary surgeon, with a primary focus on cardiovascular procedures, to provide surgical expertise and technical leadership during research, development, and evaluation of surgical devices using animate, inanimate, and cadaveric models.

Responsibilities
  • Conduct or direct surgical investigations for product development and preclinical evidence generation.
  • Use scientific and surgical expertise to evaluate functionality, efficacy, and safety of medical devices during acquisition, licensure, discovery, development, and product change evaluations.
  • Provide biomedical expertise by making unbiased recommendations to ETHICON teams regarding new technologies and interaction of device concepts on living tissue.
  • Provide technical direction and execution within Preclinical Research for surgical investigation and development of medical devices.
  • Collaborate with Preclinical Research team to apply clinically relevant models for product evaluation while meeting preclinical study design, execution, and timeline requirements.
  • Support the Preclinical Research team with the development of animal models.
  • Communicate business related issues or opportunities to next management level.
  • If supervising staff, ensure subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed are available.
  • Ensure personal and Company compliance with all Federal, State, local, and Company regulations, policies, and procedures; know and follow ETHICON policies and procedures related to work activities performed in area of responsibility.
  • Utilize interpersonal skills and collaboration to enhance team processes and drive surgical efficiency/quality within Preclinical Research, ETHICON, and J&J.
  • Function as key Preclinical Research team member by supporting department, ETHICON, and J&J goals, actively participating in and collaborating with the external scientific community.
  • Perform other duties assigned as needed.
Qualifications
  • Doctorate degree (DVM/VMD from an AVMA accredited program; MD acceptable with significant preclinical experience).
  • Surgeon residency training and board certification (DACVS) preferred.
  • Certification as Surgical Research Specialist (SRS) through the Academy of Surgical Research may be considered.
  • Demonstrated knowledge of surgical principles and theory, with specific training in cardiovascular procedures.
  • Demonstrated knowledge and experience in performing fluoroscopic angiography in large animals.
  • Experience executing preclinical and/or clinical studies, including GLP, with external contract research organizations preferred.
  • Ability to work collaboratively with the preclinical research team.
  • Familiarity with Medical Device Product Development preferred.
  • Knowledge of preclinical regulatory requirements for FDA and notified bodies outside the US preferred.
Required Skills & Experience
  • Extensive knowledge of cardiovascular surgery and interventional procedures.
  • Deep knowledge of animal and human anatomy and physiology, as well as biological systems.
  • Demonstrated analytical problemโ€‘solving and decisionโ€‘making skills.
  • Demonstrated surgical expertise during research, development, & evaluation using animate, inanimate, and cadaveric models.
  • Ability to work as a technical leader, team member, and role model for preclinical staff.
  • Excellent communication skills โ€“ written, oral, and listening.
  • Working with minimal supervision.
  • Ability to clearly document and communicate plans and results.
  • Motivated and diligent to complete studies/surgical procedures on time and with high quality.
  • Able to manage multiple tasks and responsibilities.
  • Serve as a preclinical subject matter expert on technical/surgical evaluation concerning device performance.
  • Bring new scientific principles/innovative technical solutions to projects / studies.
  • Robust surgical technique & mastery of open and laparoscopic procedures spanning multiple animal models.
  • Robotic surgical experience desired, but not required.
  • Knowledge of regulations regarding medical device development and use of live animals in preclinical research.
Other

This position is based in Cincinnati, OH, and requires up to 25% travel.

Equal Employment Opportunity

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

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