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Project Manager Biotech Jobs in Santa Rosa, CA (NOW HIRING)

Education | Experience | Skill Requirements * 10+ years of professional experience within Biotech ... Ability to prioritize and manage several complex projects simultaneously * Proven ability to ...

Sr. Scientist 1

Novato, CA

$107K - $146K/yr

Who We Are BioMarin is a leading rare disease biotechnology company focused on genetically defined ... Accountable for tracking and reporting milestones and deliverables to the CMC Project Manager.

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Project Manager Biotech information

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How much do project manager biotech jobs pay per hour?

As of Jun 25, 2026, the average hourly pay for project manager biotech in Santa Rosa, CA is $50.56, according to ZipRecruiter salary data. Most workers in this role earn between $43.89 and $55.43 per hour, depending on experience, location, and employer.

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.

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 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, and why are they important?

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.
What are popular job titles related to Project Manager Biotech jobs in Santa Rosa, CA? For Project Manager Biotech jobs in Santa Rosa, CA, the most frequently searched job titles are:
What cities near Santa Rosa, CA are hiring for Project Manager Biotech jobs? Cities near Santa Rosa, CA with the most Project Manager Biotech job openings:
Vice President, Medical Affairs

Vice President, Medical Affairs

Alumis

Bodega Bay, CA

$315K - $370K/yr

Full-time

Posted 28 days ago


Job description

Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients.

We have recently completed our pivotal trials of envudeucitinib, our second-generation tyk2 inhibitor in moderate to severe plaque psoriasis and expect results from a potentially pivotal Phase 2b trial in SLE in the third quarter of 2026.

As a key member of the Alumis team, you will provide overall leadership for the Medical Affairs function, overseeing Medical Affairs, Field Medical Liaisons, and publications. The position will liaise closely with the clinicians responsible for carrying out Alumis' clinical studies as well as our commercial group. Applicants should be a "leader/doer" capable of generating strategies and leading cross functionally. This VP, Medical Affairs will report directly to the Chief Medical Officer.


Responsibilities

Lead the Medical Affairs function at Alumis

  • Develop and implement key Medical Affairs strategies and activities to support the development of our lead assets
  • Continue to build and scale the Medical Affairs organization
  • Develop and present Medical Affairs operational plans to Development and Executive management
  • Represent company externally
  • Direct and oversee all aspects of Medical Affairs and pre-launch needs
  • Lead medical launch preparations for our lead Psoriasis candidate, ensuring the scientific narrative is robust and well-vetted.

As a member of the Development Leadership Team, run and continue to build the Medical Affairs function

  • Build and lead a best-in-class global medical affairs team to support launches of multiple indications with a focus on psoriasis for our lead asset, envudeucitinib  
  • Develop key performance indicators and generate analytical reports related to Medical Affairs plans and Medical Science Liaison group activities
  • Develop and implement Medical Communication and Disease State Awareness strategies
  • Partner with KOLs to gather information on current focused therapeutic area issues and questions
  • Collaborate with the Commercial team to develop educational material for providers and patients that are balanced and medically accurate
  • Provide direction and input into the development and implementation of successful reimbursement and market-access strategies
  • Work closely with the members of the clinical development and commercial leadership teams to develop the overall strategic direction for Alumis, evaluate alternative strategies, identify competitive issues, and develop and implement operating plans to achieve company objectives
  • Foster collaborative relationships with academic and clinical experts, publishers, medical and patient associations, and other relevant external and internal stakeholders
  • Develop and manage departmental budgets that effectively achieve desired goals and are balanced with the financial objectives of the broader organization
  • Oversee the publication strategy, ensuring clinical data is presented at major congresses (e.g., AAD, EADV, ACR) and in high-impact peer-reviewed journals.


Education | Experience | Skill Requirements

  • 10+ years of professional experience within Biotech/Pharma in Medical Affairs
  • 5+ years of people leadership experience
  • An understanding of government and industry guidelines, regulations, laws, etc., for appropriate scientific/medical exchange and communication with customers
  • Ability to lead by example, attract and develop talent, build interdependent partnerships, and create a culture of collaboration and teamwork that fosters open communication, constructive conflict resolution and organizational flexibility
  • Ability to prioritize and manage several complex projects simultaneously
  • Proven ability to develop internal relationships in a highly matrixed environment, as well as external relationships with Key Opinion Leaders and industry experts
  • Ability to communicate effectively at all levels and present complex and/or new ideas with clarity and simplicity
  • Ability to prioritize concurrent projects with tight deadlines and operate in a highly compliance-driven environment
  • Excellent written, verbal, and interpersonal skills, and the ability to communicate at all levels within the company
  • Travel (25-40%) may be required to represent the company at medical conferences, presentations, and other meetings
  • Our headquarters are located in the San Francisco Bay Area and regular presence at headquarters is required
  • Extensive prior experience in dermatology, particularly psoriasis is required. Prior experience in SLE is highly desirable. Prior experience taking a product form Phase 3 to a successful launch is also highly desirable.
  • Advanced degree (PharmD, Ph.D. or MD) is required, MD is preferred.

The salary range for this position is $315,000 USD to $370,000 USD annually. This salary range is an estimate, and the actual salary may vary based on the Company's compensation practices.