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Project Manager Biotech Jobs in Florence, KY (NOW HIRING)

Develop operational project plans; * Manage risk assessment and execution. Qualifications ... biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the ...

Develop operational project plans; * Manage risk assessment and execution. Qualifications ... biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the ...

The primary role of the Project Manager is to provide tactical management, administration, and ... biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the ...

The primary role of the Project Manager is to provide tactical management, administration, and ... biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the ...

The primary role of the Project Manager is to provide tactical management, administration, and ... biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the ...

The primary role of the Project Manager is to provide tactical management, administration, and ... biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the ...

The primary role of the Senior Project Manager is to provide tactical management, administration ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...

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Project Manager Biotech information

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$45

$75

How much do project manager biotech jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for project manager biotech in Florence, KY is $45.89, according to ZipRecruiter salary data. Most workers in this role earn between $39.86 and $50.34 per hour, depending on experience, location, and employer.

What does a project manager in biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a project manager in biotech?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.

How does a project manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

What are popular job titles related to Project Manager Biotech jobs in Florence, KY?

For Project Manager Biotech jobs in Florence, KY, the most frequently searched job titles are:

What job categories do people searching Project Manager Biotech jobs in Florence, KY look for?

The top searched job categories for Project Manager Biotech jobs in Florence, KY are:

What cities near Florence, KY are hiring for Project Manager Biotech jobs?

Cities near Florence, KY with the most Project Manager Biotech job openings:

Infographic showing various Project Manager Biotech job openings in Florence, KY as of June 2026, with employment types broken down into 1% As Needed, 7% Full Time, and 92% Part Time. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $95,459 per year, or $45.9 per hour.

AI Project Manager

Cincinnati, OH • On-site, Remote


Medpace, Inc.
Medical Equipment and Supplies Manufacturing • 1 - 5K employees

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

14th of 74 rated research

Great coworkers

People enjoy working here

Good employer


Full-time

Medical, Retirement, PTO

Re-posted 14 days ago


Job description

Job Summary

Medpace is a leading CRO in Cincinnati and is continuing to add established Project Managers to the company with a focus on Artificial Intelligence to join our Chief AI Officer (CAIO) in our Cincinnati, OH office. 

Responsibilities
  • Working across Medpace on behalf of the Chief AI Office, the individual will manage and provide accountability for day-to-day operations of the overall AI project list and ensure good communications with teams through meetings such as the AI deep dive Tech and AI working group;
  • Serve as primary AI contact for oversight of operational project-specific issues and work with teams on project deliverables;
  • Support the CAIO with global initiatives such as analysis and expansion of Microsoft Co-pilot capabilities by leading the project to communicate the latest advances to the AI working group and to collect proof points of benefits for presentation to the executive committee;
  • Support the CAIO with any requests from the organization communicating to the CAIO for questions and answers concerning the use of AI;
  • Maintain in depth knowledge of AI projects and an understanding of the latest AI capabilities;
  • Work with the CAIO to explore additional AI projects across Medpace and in the communication and dissemination of those projects to various stakeholders;
  • Provide cross-functional oversight of internal project team members and deliverables;
  • Develop operational project plans;
  • Manage risk assessment and execution.
Qualifications
  • Bachelor's degree or higher in a technical, business, or healthcare field;
  • Knowledge of clinical research is preferred;
  • 1+ years of experience as a technical or healthcare project manager;
  • Experience in the management of overall project roadmaps and timeline; and
  • Strong leadership skills with good communication.
Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience

    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Employment Type: OTHER

Medpace logo

About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992


What Medpace employees say

Pay

Benefits

Hours and flexibility

Workplace

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