... project. Previous Biotech/pharma experience is required. *** Position Description: Manage, evaluate ... and assess information related to Mechanical and Electrical systemsnecessary to construct the ...
... project. Previous Biotech/pharma experience is required. *** Position Description: Manage, evaluate ... and assess information related to Mechanical and Electrical systemsnecessary to construct the ...
... project. Previous Biotech/pharma experience is required. *** Position Description: Manage, evaluate ... and assess information related to Mechanical and Electrical systemsnecessary to construct the ...
... project. Previous Biotech/pharma experience is required. *** Position Description: Manage, evaluate ... and assess information related to Mechanical and Electrical systemsnecessary to construct the ...
Senior Project Manager
Lexington, KY · On-site
Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...
Senior Project Manager
Lexington, KY · On-site
Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...
Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...
Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...
Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...
Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...
Senior Project Manager
Lexington, KY · On-site
Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...
Senior Project Manager
Lexington, KY · On-site
Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...
Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...
Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...
CRA 1, IQVIA Biotech
$71K - $145K/yr
The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...
CRA 1, IQVIA Biotech
$71K - $145K/yr
The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...
CRA 1, IQVIA Biotech
Lexington, KY · On-site
$71K - $145K/yr
The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...
CRA 1, IQVIA Biotech
Lexington, KY · On-site
$71K - $145K/yr
The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...
Project Manager I, RWE
Louisville, KY · On-site
Creates and maintains the Trial Master File Management (TMF) Plan. Routinely reviews the TMF to ... Prior experience in a contract research organization (CRO), pharmaceutical, or biotechnology ...
New
Project Manager I, RWE
Louisville, KY · On-site
Creates and maintains the Trial Master File Management (TMF) Plan. Routinely reviews the TMF to ... Prior experience in a contract research organization (CRO), pharmaceutical, or biotechnology ...
New
... management of daily trial operations. Often functions as a global lead to provide client interface ... biotechnology, and medical device firms. For more information, visit www.ctifacts.com Why CTI?
... management of daily trial operations. Often functions as a global lead to provide client interface ... biotechnology, and medical device firms. For more information, visit www.ctifacts.com Why CTI?
... management of daily trial operations. Often functions as a global lead to provide client interface ... biotechnology, and medical device firms. For more information, visit www.ctifacts.com Why CTI?
... management of daily trial operations. Often functions as a global lead to provide client interface ... biotechnology, and medical device firms. For more information, visit www.ctifacts.com Why CTI?
Creates and maintains the Trial Master File Management (TMF) Plan. Routinely reviews the TMF to ... Prior experience in a contract research organization (CRO), pharmaceutical, or biotechnology ...
Creates and maintains the Trial Master File Management (TMF) Plan. Routinely reviews the TMF to ... Prior experience in a contract research organization (CRO), pharmaceutical, or biotechnology ...
Project Manager I - Cell & Gene Therapy (Sponsor Dedicated - US Remote; Preference for Hybrid Los An
Louisville, KY · On-site
Proficiency in clinical systems (e.g., CTMS, EDC, eTMF ) and project management tools. * Confident ... biotech leader, while maintaining CRO support and infrastructure. * Advance life-saving research
Project Manager I - Cell & Gene Therapy (Sponsor Dedicated - US Remote; Preference for Hybrid Los An
Louisville, KY · On-site
Proficiency in clinical systems (e.g., CTMS, EDC, eTMF ) and project management tools. * Confident ... biotech leader, while maintaining CRO support and infrastructure. * Advance life-saving research
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Project management experience within a biopharmaceutical company * Strong advocacy, communication ...
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Project management experience within a biopharmaceutical company * Strong advocacy, communication ...
... Regulatory Affairs, Project Management, and external customers. • Support New Product ... pharmaceutical, biotechnology, medical device, or related regulated industry. • Minimum of 3 ...
... Regulatory Affairs, Project Management, and external customers. • Support New Product ... pharmaceutical, biotechnology, medical device, or related regulated industry. • Minimum of 3 ...
... Regulatory Affairs, Project Management, and external customers. • Support New Product ... pharmaceutical, biotechnology, medical device, or related regulated industry. • Minimum of 3 ...
... Regulatory Affairs, Project Management, and external customers. • Support New Product ... pharmaceutical, biotechnology, medical device, or related regulated industry. • Minimum of 3 ...
... Regulatory Affairs, Project Management, and external customers. • Support New Product ... pharmaceutical, biotechnology, medical device, or related regulated industry. • Minimum of 3 ...
... Regulatory Affairs, Project Management, and external customers. • Support New Product ... pharmaceutical, biotechnology, medical device, or related regulated industry. • Minimum of 3 ...
... Regulatory Affairs, Project Management, and external customers. • Support New Product ... pharmaceutical, biotechnology, medical device, or related regulated industry. • Minimum of 3 ...
... Regulatory Affairs, Project Management, and external customers. • Support New Product ... pharmaceutical, biotechnology, medical device, or related regulated industry. • Minimum of 3 ...
... Regulatory Affairs, Project Management, and external customers. • Support New Product ... pharmaceutical, biotechnology, medical device, or related regulated industry. • Minimum of 3 ...
... Regulatory Affairs, Project Management, and external customers. • Support New Product ... pharmaceutical, biotechnology, medical device, or related regulated industry. • Minimum of 3 ...
Biotech Project Management information
See Kentucky salary details
$33.4K - $43.2K
2% of jobs
$43.2K - $52.9K
6% of jobs
$52.9K - $62.7K
10% of jobs
$68K is the 25th percentile. Wages below this are outliers.
$62.7K - $72.4K
13% of jobs
$72.4K - $82.2K
14% of jobs
The median wage is $85.7K / yr.
$82.2K - $91.9K
15% of jobs
$91.9K - $101.7K
13% of jobs
$103.9K is the 75th percentile. Wages above this are outliers.
$101.7K - $111.4K
12% of jobs
$111.4K - $121.2K
7% of jobs
$121.2K - $130.9K
5% of jobs
$130.9K - $140.7K
3% of jobs
$33.4K
$89.2K
$140.7K
How much do biotech project management jobs pay per year?
As of Jul 27, 2026, the average yearly pay for biotech project management in Kentucky is $89,182.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,200.00 and $106,800.00 per year, depending on experience, location, and employer.
What are the key skills and qualifications needed to thrive in the Biotech Project Management position, and why are they important?
To thrive in Biotech Project Management, you need a strong background in life sciences, experience in project planning and execution, and ideally a relevant degree (such as biology, biotechnology, or project management certification). Familiarity with project management software (like MS Project or Asana), regulatory compliance systems, and possibly certifications like PMP is often expected. Exceptional communication, leadership, problem-solving, and time management skills will help you stand out in this role. These competencies ensure projects remain on schedule, compliant, and collaborative in the fast-paced, highly regulated biotech industry.
What are the most common challenges faced by professionals in Biotech Project Management roles?
Biotech Project Management professionals often juggle cross-disciplinary teams, tight timelines, and complex regulatory requirements, which can make prioritizing tasks a challenge. Navigating scientific uncertainties and adapting to project scope changes are daily realities given the fast pace of biotech innovation. Having strong organizational and people skills helps to manage competing priorities while keeping all stakeholders aligned. By mastering these challenges, professionals can significantly contribute to the timely advancement of vital scientific initiatives.
What is a Biotech Project Management job?
A Biotech Project Management job involves overseeing and coordinating research, development, and commercialization projects in the biotechnology industry. Project managers in this field ensure that scientific, regulatory, and business objectives are met on time and within budget. They work closely with cross-functional teams, including scientists, regulatory experts, and business stakeholders, to drive project success. Strong organizational, problem-solving, and communication skills are essential for managing risks and ensuring compliance with industry regulations.
What are popular job titles related to Biotech Project Management jobs in Kentucky? For Biotech Project Management jobs in Kentucky, the most frequently searched job titles are:
What job categories do people searching Biotech Project Management jobs in Kentucky look for? The top searched job categories for Biotech Project Management jobs in Kentucky are:
Other
Posted yesterday
Turner Construction rating
7.5
Based on 69 frontline employees who took The Breakroom Quiz
31st of 80 rated construction
Job description
*** This position is for a full time traveling assignment supporting our Advanced Technology Group on a Biotech project. Previous Biotech/pharma experience is required. ***
Position Description: Manage, evaluate, and assess information related to Mechanical and Electrical systemsnecessary to construct the project on time in a safe manner, within budget, and to the qualityspecified by the contract documents.
Essential Duties & Responsibilities:
Specifically relating to the mechanical and electrical systems:- Lead the Turner project team, subcontractors, owner's consultants and representatives to ensure optimal alignment and efficient systems installation.
- Prepare and manage the contract item's list for all components, materials, and systems to ensure that all ROJ dates are in compliance with the project schedule with the appropriate approval status.
- Participate in schedule update meetings and provide the latest information for an informed and accurate schedule.
- Evaluate and manage the processing of RFI's.
- Manage the budget including the review, evaluation, and negotiation of all change orders with understanding of the financial status of all subcontractors.
- Supervise, coach and mentor Assistant MEP Engineers.
- Co-lead the MEP Coordination Process with the VDC Engineer, ensuring overall installation is in compliance with the design requirements, operations and maintenance fundamentals, and quality standards.
- Prepare scope of work documents with a division of responsibility for trades and specific scopes of work for temporary operations.
- Partner with the MEP Superintendent to resolve conflicts between the mechanical and electrical systems with the site logistics plan and in compliance with the project schedule.
- Co-lead with the MEP Superintendent the overall turnover process including start-up, testing, commissioning and closeout.
- Conduct regular project walkthroughs with the MEP staff to ensure that work is proceeding in accordance with the contract documents, coordination drawings, and approved submittals.
- Identify and inform field staff of difficult installation requirements in sufficient time to allow for proper planning and execution.
- Manage and secure all municipal and agency documentation required for temporary certificates of information and system operation.
- Create and implement the quality control plan with the MEP Superintendent.
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About Turner Construction
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Turner Construction, headquartered in New York, NY, US, is a recognized leader in the construction industry. It was established in 1902 and has since curved its niche as one of the most reputable construction firms. Turner Construction provides a broad range of services like general contracting, construction management, design-build, and consulting. Devoted to environment-friendly building practices, it is considered a pioneer in green building and sustainability efforts. Their top-tier projects include Madison Square Garden, Yankee Stadium, and the United Nations Secretariat Building in New York City. The company's mission is to deliver an exceptional product by relentless commitment to their core principles – teamwork, integrity, commitment, and community.
Industry
Construction
Company size
10,000+ Employees
Headquarters location
New York, NY, US
Year founded
1902