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Biological Project Manager Jobs in Riverside, CA

JenaValve

Project Manager, Regulatory Affairs

Irvine, CA · On-site

$130K - $140K/yr

Job Title : Project Manager, Regulatory Affairs Supervisor/Manager Title: Senior Manager ... Bachelor's degree in a scientific discipline (engineering, biology, etc.) or equivalent is required.

Stantec

Senior Biologist

Irvine, CA · On-site

Demonstrable experience in all aspects of project management, biological impact assessment and mitigation strategy development, and preparation and review of biological resources documents.

Stantec

Associate Biologist/Botanist

San Bernardino, CA · On-site

$62K - $90K/yr

Lead and mentor project field teams and provide support to project managers undertaking renewable ... Experience in preparing technical documentation including biological survey reports, technical ...

Stantec

Senior Biologist On-Call

San Bernardino, CA · On-site

The candidate will work closely with project managers, scientists, engineers, and other specialists with the development and delivery of biological studies for projects involving electric ...

Stantec

Associate Biologist On-Call

Irvine, CA · On-site

The candidate will work closely with project managers, scientists, engineers, and other specialists with the development and delivery of biological studies for projects involving electric ...

Stantec

Senior Biologist On-Call

Irvine, CA · On-site

The candidate will work closely with project managers, scientists, engineers, and other specialists with the development and delivery of biological studies for projects involving electric ...

Stantec

Associate Biologist/Botanist

San Bernardino, CA · On-site

$65 - $95/hr

Stantec is seeking a consulting biologist with a minimum of 5 years of experience to join our ... Lead and mentor project field teams and provide support to project managers undertaking renewable ...

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All JobsBiological Project JobsBiological Project Manager JobsBiological Project Manager Jobs in Riverside, CA

Biological Project Manager information

See Riverside, CA salary details

$27

$59

$83

How much do biological project manager jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for biological project manager in Riverside, CA is $59.83, according to ZipRecruiter salary data. Most workers in this role earn between $50.38 and $71.20 per hour, depending on experience, location, and employer.

What is a biological project manager?

Biological Project Managers are professionals who oversee and coordinate biological research projects, ensuring they are completed on time, within scope, and on budget. They work with scientists, research teams, and other stakeholders to plan, execute, and monitor projects involving biology-related tasks, such as laboratory research, field studies, or product development. Their responsibilities often include resource allocation, risk management, and communication between different departments or organizations. They play a crucial role in facilitating collaboration and ensuring that scientific goals are met efficiently.

How does a biological project manager typically coordinate with cross-functional teams during a project's lifecycle?

Biological Project Managers frequently collaborate with scientists, regulatory experts, quality assurance professionals, and external partners to keep projects on track. They facilitate communication between these groups, ensuring everyone is aligned on goals, timelines, and compliance requirements. Regular meetings, status reports, and shared project management tools are commonly used to address challenges and adapt to shifting priorities. This cross-functional coordination is crucial for the timely and successful completion of complex biological research and development projects.

What are the key skills and qualifications needed to thrive as a biological project manager, and why are they important?

To thrive as a Biological Project Manager, you need a solid background in biology or life sciences, project management experience, and a relevant degree (often a master's or higher). Familiarity with project management software (such as MS Project or Asana), laboratory management systems, and sometimes certifications like PMP are typical requirements. Exceptional organizational skills, leadership, and effective communication are vital soft skills for coordinating teams and stakeholders. These competencies ensure that complex biological projects are completed efficiently, on time, and within budget while meeting scientific and regulatory standards.

What is the difference between Biological Project Manager vs Biological Scientist?

AspectBiological Project ManagerBiological Scientist
Required CredentialsBachelor's or Master's in Biology, Project Management certification often preferredDegree in Biology or related field, Ph.D. often preferred
Work EnvironmentProject teams, laboratories, research facilitiesLaboratories, research institutions, universities
Employer & Industry UsageBiotech companies, pharmaceutical firms, research organizationsAcademic institutions, research labs, biotech companies

The main difference is that Biological Project Managers oversee research projects, coordinating teams and resources, while Biological Scientists focus on conducting experiments and research. Both roles require biology expertise, but project managers emphasize planning and management, whereas scientists focus on scientific discovery.

What are popular job titles related to Biological Project Manager jobs in Riverside, CA?

For Biological Project Manager jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Biological Project Manager jobs in Riverside, CA look for?

The top searched job categories for Biological Project Manager jobs in Riverside, CA are:

Biological Project Manager jobs near you

Project Manager, Regulatory Affairs

JenaValve

Irvine, CA • On-site

$130K - $140K/yr

Full-time

Posted 26 days ago

Key responsibilities

  • Prepare timely, high-quality regulatory documentation and submissions for investigational device applications, commercial registrations, and amendments.

  • Collaborate with stakeholders to develop technical, clinical, or labeling content to support regulatory submissions and ensure global requirements are met.

  • Communicate with regulatory bodies, legal agents, distributors, and suppliers to obtain necessary regulatory approvals and support post-market surveillance activities.

Job description

Job Title: Project Manager, Regulatory Affairs
Supervisor/Manager Title: Senior Manager, Regulatory Affairs
Job Location & Environment: Remote
Job Description Summary: Responsible for timely preparation and submission of organized, scientifically valid global regulatory affairs submissions (clinical, pre-, and post-market applications), query responses and correspondence tracking. Maintains regulatory information for competitive intelligence, literature maintenance, and standards review programs. Interacts with internal departments and external representatives (i.e., distributors, legal agents, regulatory agencies). Provides expertise in translating regulatory requirements into practical, workable strategy and planning documents. Provides counsel to project team members and regulatory affairs staff as applicable. Supports serious adverse event reporting, and completion of post-market surveillance activities (complaints, MDR and vigilance reports). Performs other projects and duties as assigned.
Job Responsibilities:
  • Prepare timely, high-quality, technical documentation and regulatory submissions for investigational device applications, commercial registrations, annual reports, and amendments/supplements.
  • Serve as a regulatory team member of product development and sustaining teams, providing clear, concise regulatory strategy to ensure applicable global requirements are met for product development and quality system projects.
  • Collaborate with key stakeholders to develop technical, clinical, or labeling content (including Clinical Operations, Marketing, R&D, Manufacturing and Quality) to support company objectives and regulatory submissions.
  • Provide coaching and support to other members of the regulatory department.
  • Communicate with regulatory bodies, legal agents, distributor partners, and suppliers on project-related activities necessary to ensure appropriate regulatory approvals are in place in covered regions.
  • Review document change orders for impact on US, EU and international regulatory filings per standard procedures.
  • Manage standards review process and assist company SME's to interpret existing or new regulatory requirements for company products and procedures, labeling, marketing projects, clinical studies, testing, and record keeping.
  • Support serious adverse event reporting process, Medical Device Reports (MDRs), Vigilance reports, field safety notices, and other communication with regulatory authorities and external stakeholders.
  • Review and approve FMEAs/risk analyses, protocols, reports, NCRs, CAPAs, and other technical documents.
  • Participate in internal audits and external audits as needed.
  • Update and maintain departmental procedures as required.
  • Perform other duties as assigned.

Required Education and Experience:
  • Bachelor's degree in a scientific discipline (engineering, biology, etc.) or equivalent is required.
  • Minimum of 5 to 8 years in medical device Regulatory Affairs.
  • Experience with US Class III cardiovascular devices preferred.
  • Experience with EU MDR implementation preferred.
  • Comprehensive knowledge of quality systems and relationship to business.
  • Experience in applying global medical device regulations and product development process.
  • Ability to interpret regulatory standards and guidance and provide direction to project teams.
  • Ability to work in a fast-paced, technically challenging environment where drive is critical to success.
  • Self-motivated and self-disciplined; able to prioritize multiple tasks and responsibilities.
  • Effective interpersonal skills/diplomacy and problem-solving techniques.
  • Excellent applied thinking and technical writing skills.
  • Strong communication and organization skills required.

Skills and Abilities Required for This Job:
  • Strong verbal and written communication, organization, and project management skills required.
  • Works on problems of diverse scope and analyzes data and information to make sound decisions, recommendations, and regulatory filings of high quality.
  • Self-directed with minimum instruction on routine work, and general instruction on new assignments.
  • Ability to handle challenges and uncertain circumstances, with adaptability to shifting company priorities.
  • Exercises good judgment within generally defined practices and policies in all aspects of the job.
  • Diplomacy and cultural sensitivity are essential attributes.
  • Software proficiency in Microsoft Office Suite.
  • The employee must occasionally lift and/or move up to 20 pounds.

Physical Requirements:
  • Ability to travel up to 20%.

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