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Project Manager Biotech Jobs in Oklahoma (NOW HIRING)

Senior IT Portfolio & Governance Lead

Tulsa, OK ยท On-site +1

$119K - $120K/yr

... biotechnology? AtCepheid,one ofDanaher's15+ operating companies, our work saves lives-and we're all ... The position partners with project managers, resource managers, and business stakeholders to ...

It is key to our becoming one of the world's leading biotechnology companies. We are global ... Project and Program management and phenomenal communication skills * Degree educated THRIVE What ...

Manage project scope, budget, delivery risks, quality assurance, and stakeholder communications ... Biotech operations * Clinical supply management * Batch manufacturing * Product traceability

Strategic Sourcing Manager

Oklahoma City, OK ยท On-site

$119K - $155K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Project Management Experience - able to lead teams that cut across geographic and functional ...

... scope projects with site and regional impact - Build and execute productivity plans through ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

... scope projects with site and regional impact - Build and execute productivity plans through ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

... scope projects with site and regional impact - Build and execute productivity plans through ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

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Project Manager Biotech information

See Oklahoma salary details

$20

$42

$70

How much do project manager biotech jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for project manager biotech in Oklahoma is $42.70, according to ZipRecruiter salary data. Most workers in this role earn between $37.07 and $46.83 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 Oklahoma?

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

What cities in Oklahoma are hiring for Project Manager Biotech jobs?

Cities in Oklahoma with the most Project Manager Biotech job openings:

Infographic showing various Project Manager Biotech job openings in Oklahoma as of August 2026, with employment types broken down into 89% Full Time, 10% Part Time, and 1% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $88,810 per year, or $42.7 per hour.

Senior Program Manager / Wheeler Bio

Oklahoma City, OK โ€ข On-site

$90 - $130/hr

Other

Posted 12 days ago


Job description

Description

Important: This role requires handsโ€‘on project leadership experience in regulated pharmaceutical, biotechnology, or aerospace environments, including direct oversight of manufacturing or technical operations. Candidates without this background will not be considered.

Position Overview

Seeking a driven and resourceful Senior Program Manager to lead complex multi-phase biologics development and manufacturing projects within a CDMO environment. As part of the Commercial team, this position is accountable for the planning and successful delivery of projects in alignment with contracted commitment to clients, regulatory requirements, and Wheelerโ€™s revenue goals. Acting as the primary point of contact for clients, the Senior Program Manager will manage timelines, budgets, resources, and crossโ€‘functional project teams. This role requires a strategic mindset with exceptional organizational, communication, and critical thinking skills.

Key Responsibilities

Project Leadership & Execution: Lead process development and/or GMP manufacturing projects with endโ€‘toโ€‘end oversight, managing all project phases to ensure adherence to timelines, budget, quality, and regulatory standards. Develop and maintain Project Plans to manage critical path activities and drive onโ€‘time delivery of revenue generating milestones. Effectively handle changes by evaluating and managing change orders, assessing their impact, and ensuring proper documentation, approval, and stakeholder communication.

Client Management: Establish and maintain strong relationships with clients through proactive engagement and clear, concise communication throughout project cycle.

Crossโ€‘functional Collaboration: Work closely with process development, manufacturing, quality assurance, regulatory, supply chain, and thirdโ€‘party vendors to coordinate resources and ensure alignment on project deliverables. Partner with the Finance Team to ensure accurate and timely completion of financial transactions.

Risk Management: Proactively identify, assess, and mitigate project risks to ensure project continuity. Develop contingency plans and address potential roadblocks to project success.

Performance Reporting: Generate regular project status reports and documentation to provide stakeholders with visibility into project progress, variances, challenges, and successes.

Continuous Improvement: Identify areas for process improvement and contribute to the development of best practices to enhance organizational efficiency and project outcomes.

Qualifications

Education: Bachelorโ€™s degree in Life Sciences, Engineering, or a related field. Advanced degree and/or PMP certification is a plus.

Experience: 3+ years in people leadership and 5+ years in project/program management in regulated pharmaceutical, biotechnology or aerospace environments. Experience in Technical Operations in both productโ€‘based and serviceโ€‘based settings is highly desirable.

Technical Knowโ€‘How: Keen understanding of biologics processes, cGMP manufacturing, supply chain, and regulatory requirements. Expertise in Lean and other process improvement methodologies, with a proven track record of delivering measurable results is a plus.

Ideal Candidate
  • Proficient in project management tools (e.g., MS Project, Smartsheet) for effective timeline and resource management.
  • Master communicator, with ability to navigate stakeholder conflicts and negotiate for best outcomes.
  • Critical thinker; able to apply analytical techniques to solve for array of project challenges.
  • Solid decisionโ€‘maker; adopts dataโ€‘informed approach in guiding Teams methodically to better outcomes.
  • Adaptable; able to thrive in a fastโ€‘paced, dynamic environment and pivot quickly when faced with changing business priorities and tight deadlines.
  • Committed to continuous learning and professional development, with a growth mindset and a passion for excellence.
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