ZipRecruiter

Log In

1

Senior Director Medical Device Jobs (NOW HIRING)

Kellton Tech

Medical Device Assembler

Madison, WI · On-site

$23 - $24/hr

Medical device, pharmaceutical industry Competencies: Self-directed Teamwork Good communication skills Proficient with computer systems Critical thinking Decision making Quality focused ...

Ideayabio

Senior Director, Medical Writing

San Diego, CA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

IDEAYA is seeking a highly motivated, well-organized, and skilled Senior Director, Medical Writing to provide strategic and operational leadership across oncology programs spanning early- and late ...

Centene

Senior Director, Medical Economics

OR · On-site +1

$148K - $274K/yr

  • Medical

  • Retirement

  • PTO

The Senior Director, Medical Economics leads analytic service delivery by aligning strategic objectives with the development of tools and capabilities and appropriate deployment of supporting ...

New

Socket.dev

Senior Director, Medical Economics

Nevada, IA · On-site

$148 - $274/hr

  • Medical

  • Retirement

  • PTO

The Senior Director, Medical Economics leads analytic service delivery by aligning strategic objectives with the development of tools and capabilities and appropriate deployment of supporting ...

New

Cellectis

Senior Director, Medical Affairs

Manhattan, NY · On-site

$175/hr

Clinical Development Position Summary Cellectis is seeking a highly experienced Senior Director, Medical Affairs to help shape and operationalize the company's medical affairs strategy across its ...

Centene

Senior Director, Medical Economics

$148K - $274K/yr

  • Medical

  • Retirement

  • PTO

The Senior Director, Medical Economics leads analytic service delivery by aligning strategic objectives with the development of tools and capabilities and appropriate deployment of supporting ...

New

previous pagenext page

Showing results 21-40

All JobsBusiness JobsProduct Development JobsProduct Manager JobsSenior Director Medical Device Jobs

Senior Director Medical Device information

See salary details

$39.5K

$142.9K

$279.5K

How much do senior director medical device jobs pay per year?

As of Aug 17, 2026, the average yearly pay for senior director medical device in the United States is $142,920.00, according to ZipRecruiter salary data. Most workers in this role earn between $101,500.00 and $161,000.00 per year, depending on experience, location, and employer.

What does a senior director in medical device do?

A Senior Director in Medical Device leads and manages teams responsible for the development, regulatory approval, and commercialization of medical devices. They oversee product strategy, ensure compliance with industry regulations, and collaborate with cross-functional teams such as R&D, marketing, and quality assurance. Their role also involves setting department goals, managing budgets, and building relationships with key stakeholders to drive business growth.

How does a senior director in medical device typically collaborate with cross-functional teams to drive product development?

As a Senior Director in Medical Device, you will regularly collaborate with diverse teams such as R&D, regulatory affairs, quality assurance, marketing, and manufacturing. Your role involves facilitating communication between departments to ensure product development aligns with both regulatory standards and market needs. You’ll often lead cross-functional meetings, set project priorities, and resolve bottlenecks to keep projects on track. This collaborative environment is crucial for successfully bringing innovative medical devices to market while meeting strict compliance and quality requirements.

What are the key skills and qualifications needed to thrive as a senior director in medical device, and why are they important?

To thrive as a Senior Director in Medical Devices, you need extensive experience in product development, regulatory compliance, and a strong background in life sciences or engineering, often supported by an advanced degree. Familiarity with FDA regulations, ISO standards, quality management systems, and project management tools is typically required. Leadership, strategic thinking, and excellent communication are essential soft skills for guiding cross-functional teams and driving innovation. These skills ensure the safe, compliant, and successful delivery of medical devices in a highly regulated and competitive industry.
More about Senior Director Medical Device jobs

What cities are hiring for Senior Director Medical Device jobs?

Cities with the most Senior Director Medical Device job openings:

What states have the most Senior Director Medical Device jobs?

States with the most job openings for Senior Director Medical Device jobs include:

What job categories do people searching Senior Director Medical Device jobs look for?

The top searched job categories for Senior Director Medical Device jobs are:

Senior Director Medical Device jobs near you
Infographic showing various Senior Director Medical Device job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $142,920 per year, or $68.7 per hour.

Director / Sr. Director, Medical Monitor

Artiva Biotherapeutics, Inc.

San Diego, CA • On-site

$250K - $350K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 17 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.

Apply