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Director Medical Biotechnology Jobs (NOW HIRING)

BESTMSLs

Field Director, Medical Affairs

Manhattan, NY · On-site

Director, Medical Science Liaison BESTMSLs Overview Uniphar BESTMSLs is excited to partner with an ... or biotech company, with meaningful field medical leadership experience • Demonstrated track ...

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How much do director medical biotechnology jobs pay per year?

As of Aug 11, 2026, the average yearly pay for director medical biotechnology in the United States is $232,369.00, according to ZipRecruiter salary data. Most workers in this role earn between $198,000.00 and $284,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a director medical biotechnology?

To thrive as a Director of Medical Biotechnology, you need advanced expertise in molecular biology, drug development, and regulatory compliance, typically backed by a PhD or equivalent in a relevant scientific field and significant leadership experience. Familiarity with laboratory information management systems (LIMS), clinical trial management software, and knowledge of FDA or EMA regulatory frameworks are crucial. Strategic thinking, strong communication, and team leadership are vital soft skills for guiding multidisciplinary teams and driving innovation. These capabilities ensure effective oversight of complex projects, regulatory adherence, and successful advancement of biotechnological products to market.

What is the difference between Director Medical Biotechnology vs Senior Medical Scientist?

AspectDirector Medical BiotechnologySenior Medical Scientist
Required CredentialsAdvanced degrees (PhD, MD), leadership experienceMaster's or PhD, specialized scientific expertise
Work EnvironmentLeadership roles in R&D, biotech companies, or pharma firmsLaboratories, research teams, clinical settings
Employer & Industry UsageBiotech firms, pharmaceutical companies, research institutionsResearch labs, clinical research organizations, biotech companies
Common Search & ComparisonOften compared for leadership and strategic rolesCompared for scientific expertise and research focus

The main difference between a Director Medical Biotechnology and a Senior Medical Scientist lies in their responsibilities and seniority. The Director oversees strategic planning, manages teams, and makes high-level decisions, while the Senior Medical Scientist focuses on conducting research, experiments, and scientific analysis. Both roles require advanced degrees and industry experience, but the Director typically has more leadership and managerial duties.

What does a director medical biotechnology do?

A Director of Medical Biotechnology oversees research and development activities in biotechnology organizations, focusing on medical applications such as drug development, diagnostics, and therapeutic solutions. They lead teams of scientists and researchers, manage budgets, ensure compliance with regulatory standards, and set strategic goals for innovation and commercialization. This role also involves collaborating with other departments, external partners, and stakeholders to bring new medical technologies from concept to market. Directors must stay updated on industry trends and scientific advances to guide their organizations effectively.

What are the main challenges a director medical biotechnology faces when leading cross-functional teams in product development?

A Director of Medical Biotechnology often encounters challenges in aligning diverse teams—such as research scientists, regulatory affairs, and commercial departments—toward common project goals. Effective communication and coordination are crucial, as priorities and timelines may differ across functions. Additionally, navigating regulatory requirements while driving innovation and ensuring product safety adds complexity to decision-making. Successful directors foster collaboration, mediate conflicts, and ensure all stakeholders are informed and engaged throughout the development cycle.
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Director Medical Biotechnology jobs near you
Infographic showing various Director Medical Biotechnology job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $232,369 per year, or $111.7 per hour.

Director / Sr. Director, Medical Monitor

Artiva Biotherapeutics

San Diego, CA • Remote

$250K - $350K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 9 days ago

Job description

About Artiva:

We are a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies. Our mission is to develop effective, safe, and accessible cell therapies for patients with devastating autoimmune diseases. We aim to develop therapies that patients and physicians can utilize in a community setting. Our lead product candidate, AlloNK®, is a non-genetically modified, cryopreserved NK cell therapy being evaluated in combination with B-cell targeted monoclonal antibodies (mAbs). We believe the compelling cell killing properties of NK cells, when combined with mAbs for targeting, creates an opportunity to generate potentially transformative therapies.


For more information, visit www.artivabio.com.


Job Summary:

The Senior Director/Sr. Director, Medical Monitor provides medical oversight and safety monitoring across Artiva's clinical trials, ensuring participant safety, data integrity, and regulatory compliance throughout study conduct. This role requires an experienced physician with strong clinical judgment and hands-on medical monitoring experience in Phase 2-3 studies, who collaborates effectively across functions while thriving in a fast-moving biotech environment.

Duties/Responsibilities:

  • Provide ongoing medical monitoring and safety oversight for assigned clinical trials, including real-time review of safety data, adverse events, and laboratory findings.
  • Serve as the primary medical point of contact for investigators and sites on eligibility, protocol interpretation, and patient management questions.
  • Engage with investigators, advisors, and external experts to support trial execution and clinical oversight.
  • Review and assess adverse events and serious adverse events, including causality assessment, and support safety signal detection in partnership with Pharmacovigilance.
  • Conduct ongoing medical and clinical data review, including data listings, protocol deviations, and eligibility, to ensure data quality and participant safety.
  • Provide clinical input into protocols, amendments, informed consent forms, and other study-related documents.
  • Review and interpret clinical and safety data to inform protocol adjustments and trial-level decisions.
  • Develop and maintain medical monitoring plans and safety review processes for assigned studies.
  • Partner closely with Clinical Operations and CROs on trial conduct, site management, and medical monitoring activities.
  • Partner with Biometrics and Regulatory Affairs to ensure clinical data supports statistical and regulatory requirements.
  • Collaborate closely with Translational Medicine, Safety/Pharmacovigilance, Regulatory Affairs, Biometrics, Medical Affairs, and CMC teams.
  • Provide clinical input into biomarker and safety strategies.
  • Contribute to safety reports, DSURs, and responses to health authority questions.
  • Provide clinical input into briefing documents, responses to regulatory questions, and clinical components of submissions.
  • Support readiness for audits, inspections, and regulatory review.

Requirements:

  • MD required.
  • Hands-on medical monitoring experience in Phase 2-3 clinical trials in rheumatology or immunology indications required.
  • Background in immunology, autoimmune disease, rheumatology or cell therapy required.
  • Rheumatologist with Board certification preferred.
  • 5+ years of clinical development and/or medical monitoring experience in biotechnology and/or pharmaceutical organizations.
  • Experience supporting programs through key clinical trial milestones (e.g., study start-up, interim analyses, pivotal study conduct).
  • Strong ability to integrate clinical, safety, and scientific data into sound clinical and risk-benefit decisions.
  • Solid understanding of global clinical development, GCP, and patient safety requirements.
  • Clear and credible communicator with investigators, cross-functional teams, senior management, and external experts.
  • Familiarity with regulatory submissions (e.g., NDA, BLA, MAA) and support of health authority interactions.
  • Comfortable operating as an individual contributor in a lean, fast-moving biotech environment
  • Models transparency, collaboration, and patient-centric decision-making.

In addition to a great culture, we offer:

  • A beautiful facility 
  • An entrepreneurial, highly collaborative, and innovative environment
  • Comprehensive benefits, including:
  • Medical, Dental, and Vision
  • Group Life Insurance
  • Long Term Disability (LTD)
  • 401(k) Retirement Plan
  • Employee Assistance Program (EAP)
  • Flexible Spending Account (FSA)
  • Paid Time Off (PTO)
  • Company paid holidays, including the year-end holiday week
  • Our recognition program, Bonus.ly, is where you can trade in points earned for things you want.


If all this speaks to you, come join us on our journey!


Base Salary: $250,000 - 350,000. Exact compensation may vary based on skills and experience.