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Preclinical Project Manager Jobs in Ohio (NOW HIRING)

GMP Senior Scientist

Columbus, OH ยท On-site

$85K - $116K/yr

... 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 ...

Supervisor, Necropsy

Ashland, OH ยท On-site

$70K/yr

Manager inventory and supply ordering. * Oversee development of special procedures (technical ... projects. * Assist with training staff and development of soft skills. * Assist pathology ...

New

... clinical and preclinical candidates in development for various psychiatric and neurological ... Document Management System Support. * Support documentation lifecycle (Document Scanning ...

Document Management System Support. * Support documentation lifecycle (Document Scanning ... Support area initiatives and projects. Skills / Abilities: * Experience in Pharmaceutical Quality ...

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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 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.

Scientist, Preclinical Research, Robotics & Digital Solutions - MedTech Surgery

Cincinnati, OH โ€ข On-site

Other

Retirement, PTO

Posted yesterday

New


Job description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function

Discovery & Pre-Clinical/Clinical Development

Job Sub Function

Animal Medicine

Job Category

Scientific/Technology

All Job Posting Locations:

Cincinnati, Ohio, United States of America

Job DescriptionAbout Surgery

Fueled by innovation at the intersection of biology and technology, weโ€™re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of MedTech surgery? Ready to join a team thatโ€™s reimagining how we heal? Our MedTech Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the worldโ€™s most prevalent conditions such as obesity, cardiovascular disease and cancer. Patients are waiting. Your unique talents will help patients on their journey to wellness.

Johnson & Johnson MedTech Surgery is recruiting for a Scientist, Preclinical Research, Robotics & Digital Solutions, located in Cincinnati, Ohio. This position has the unique opportunity to support Preclinical activities within the Johnson & Johnson MedTech Surgery Robotics program.

Purpose

Johnson & Johnson MedTech has been working to make surgery better for more than a century. With substantial breadth and depth in surgical technologies, orthopedic and interventional solutions, we aspire to improve and enhance medical care for people worldwide. Together, we are working to shape the future of health through differentiated products and services.

Johnson & Johnsonโ€™s long-term vision is to use digital technology as part of a holistic approach to surgery across the episode of care to enhance surgical efficiency, promote better clinical outcomes and increase patient satisfaction. This position will serve as a scientific contributor for the development and execution of preclinical evidence strategies necessary to competitively position a product for domestic and international regulatory and clinical acceptance.

You Will Be Responsible For
  • Supports product evaluations involving animate, inanimate, and cadaveric models
  • Performs research supporting development of products or procedures in minimally invasive robotic surgery
  • Assisting or conducting investigations for medical device development and preclinical evidence generation aligned to R&D, Regulatory, and Commercial needs
  • Coordinate and ensure accurate documentation of laboratory activities
  • Conduct lab activities in compliance with USDA, AAALAC, and J&J Animal use policies
  • Ensure compliance with 21 CFR Part 58 โ€“ Good Laboratory Practices
  • Contribute and support the design of appropriate studies to meet premarket and postmarket needs
  • Design, plan and execute preclinical animal studies for the assessment of safety, performance, and effectiveness
    • Act as study coordinator in support of the Study Director
    • May act as Study Director on less complex projects
  • Assess, communicate, and manage the risks associated to the preclinical evaluation of products.
  • Assist in appropriate interpretation and dissemination of all evidence generated, based on evidence dissemination strategy, including study reports, abstracts, manuscripts, etc.
  • Demonstrate the ability to work effectively in a team-oriented environment that embraces ownership and accountability for innovation, change, risk, and flexibility
  • Build successful relationships internally and develop partnerships with key business partners
  • May require up to 15% domestic and international travel
Qualifications / Requirements
  • A minimum of a bachelorโ€™s degree in Biological Science or a related discipline
  • A minimum of 3 years of related scientific / technical experience within preclinical research
  • Experience in preclinical science and processes along with an understanding of medical device development processes, related healthcare market environment, clinical trends, and preclinical regulations
  • Track record of contributing to preclinical programs on time, within budget and in compliance to SOPs and regulations
  • Experience working in a GLP environment and direct experience executing preclinical studies
  • Understanding of good documentation practices
  • Familiarity with animal welfare regulations and IACUC
Preferred
  • Experience working in Medical Devices or Robotics
  • Experience working with large animal models
  • Experience in support of global regulatory submissions for medical devices, biologics, or drugs (including PMA/BLA/NDA and/or their global counterparts)
Benefits

Subject to the terms of their respective plans, employees are eligible to participate in the Companyโ€™s consolidated retirement plan (pension) and savings plan (401(k)).

This position is eligible to participate in the Companyโ€™s long-term incentive program.

Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:

  • Vacation โ€“120 hours per calendar year
  • Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado โ€“48 hours per calendar year; for employees who reside in the State of Washington โ€“56 hours per calendar year
  • Holiday pay, including Floating Holidays โ€“13 days per calendar year
  • Work, Personal and Family Time - up to 40 hours per calendar year
  • Parental Leave โ€“ 480 hours within one year of the birth/adoption/foster care of a child
  • Bereavement Leave โ€“ 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
  • Caregiver Leave โ€“ 80 hours in a 52-week rolling period10 days
  • Volunteer Leave โ€“ 32 hours per calendar year
  • Military Spouse Time-Off โ€“ 80 hours per calendar year

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.

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.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicantsโ€™ needs. If you are an individual with a disability and would like to request an accommodation, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.

If you are under 18 years of age you (the candidate) may need to obtain the necessary working papers or other documentation required by state law to start the assignment, as well as get a parentโ€™s consent for the background check

Preferred Skills:

Analytical Reasoning, Clinical Trial Protocols, Data Savvy, Detail-Oriented, Drug Discovery Development, Quality Control (QC), Research Ethics, Researching, Scientific Research, Supervision, Technologically Savvy, Unflappability, Use of Laboratory Equipment, Veterinary Care, Veterinary Medicine, Veterinary Sciences, Vivarium Management

The anticipated base pay range for this position is :

$92,000.00 - $148,350.00

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