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Director Medical Device Clinical Research Jobs (NOW HIRING)

Noctrix Health

Director, Clinical Affairs

Pleasanton, CA · On-site

$89K - $121K/yr

The Director, Clinical Affairs will serve as a key cross-functional leader and liaison among ... Minimum of 8 years of clinical affairs or clinical research experience within the medical device ...

Noctrix Health

Director, Clinical Affairs

Pleasanton, CA · On-site

$89K - $121K/yr

The Director, Clinical Affairs will serve as a key cross-functional leader and liaison among ... Minimum of 8 years of clinical affairs or clinical research experience within the medical device ...

Provident Research Inc

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Senior Clinical Research Associate Cardiac Medical Device

Phoenix, AZ · Remote

$135K - $141K/yr

SR CRA Cardiac Medical Device (home based) Remote Become Part of a Major Initiative to Monitor Life ... clinical research areas Relevant industry certifications preferred (i.e. CCRA, RAC, CDE ...

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Director Medical Device Clinical Research information

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How much do director medical device clinical research jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for director medical device clinical research in the United States is $54.33, according to ZipRecruiter salary data. Most workers in this role earn between $32.45 and $71.63 per hour, depending on experience, location, and employer.

What does a director of medical device clinical research do?

A Director of Medical Device Clinical Research oversees the planning, execution, and management of clinical trials for medical devices. They ensure that studies comply with regulatory requirements, manage clinical research teams, and collaborate with cross-functional departments such as regulatory affairs, quality assurance, and product development. Their responsibilities also include developing clinical strategies, ensuring patient safety, overseeing data analysis, and communicating results to stakeholders. The ultimate goal is to ensure that medical devices are safe, effective, and meet all regulatory standards before reaching the market.

What are the key skills and qualifications needed to thrive as a director of medical device clinical research?

To thrive as a Director of Medical Device Clinical Research, you need advanced expertise in clinical trial design, regulatory compliance, and medical device development, typically supported by a relevant advanced degree (e.g., MD, PhD, or MS) and significant industry experience. Familiarity with tools like EDC (electronic data capture) systems, clinical trial management software, and understanding of FDA and ISO regulatory frameworks are essential. Strong leadership, strategic thinking, and excellent communication skills set top candidates apart by enabling effective team management and cross-functional collaboration. These competencies are crucial for ensuring rigorous study execution, regulatory approval, and successful product development in a highly regulated environment.

What are some common challenges faced by a director of medical device clinical research, and how can they be managed?

A Director of Medical Device Clinical Research often encounters challenges such as navigating complex regulatory requirements, ensuring robust clinical trial design, and managing cross-functional teams spread across multiple locations. Effective communication with regulatory bodies, proactive risk management, and fostering strong collaboration between clinical, regulatory, and product development teams are key to overcoming these hurdles. Staying updated on evolving industry standards and leveraging project management tools can further streamline trial execution and maintain compliance.

What is the difference between Director Medical Device Clinical Research vs Clinical Research Manager?

AspectDirector Medical Device Clinical ResearchClinical Research Manager
CredentialsTypically requires advanced degrees (e.g., MS, PhD), industry certifications, and extensive experienceRequires a bachelor's or master's degree in life sciences or related field, with relevant experience
Work EnvironmentOversees multiple clinical trials, manages teams, and interacts with regulatory bodiesManages day-to-day clinical trial operations, coordinates sites, and ensures protocol compliance
Employer & Industry UsageCommonly employed by medical device companies, biotech firms, and CROsFound in similar settings, often reporting to directors or senior managers

The main difference is that the Director Medical Device Clinical Research holds a higher strategic and leadership role, overseeing multiple projects and teams, while the Clinical Research Manager focuses on operational management of individual trials. Both roles require relevant experience and industry knowledge, but the director position involves broader oversight and strategic planning.

What cities are hiring for Director Medical Device Clinical Research jobs?

Cities with the most Director Medical Device Clinical Research job openings:

What are the most commonly searched types of Medical Device Clinical Research jobs?

The most popular types of Medical Device Clinical Research jobs are:

What states have the most Director Medical Device Clinical Research jobs?

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

Director Medical Device Clinical Research jobs near you
Infographic showing various Director Medical Device Clinical Research job openings in the United States as of June 2026, with employment types broken down into 3% As Needed, 38% Full Time, 28% Part Time, 3% Temporary, and 28% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $113,010 per year, or $54.3 per hour.

Director, Clinical Affairs

Noctrix Health

Pleasanton, CA • On-site

$89K - $121K/yr

Full-time

Posted 6 days ago

Job description

Noctrix Health is redefining the treatment of chronic neurological disorders with clinically validated therapeutic wearables. Our team of medical device specialists, neuroscientists, and consumer electronics engineers is dedicated to delivering prescription-grade therapy with an outstanding user experience. We have pioneered the world's first drug-free wearable therapy, clinically proven to alleviate symptoms in adults with drug-resistant Restless Legs Syndrome (RLS). Join us in transforming healthcare, improving lives, and driving meaningful change through innovative medical technology.
We are seeking an experienced and strategic Director, Clinical Affairs to lead the planning, execution, and oversight of clinical studies supporting the development, regulatory approval, reimbursement, and commercialization of Noctrix Health's medical devices. This leader will be accountable for the successful delivery of clinical programs, ensuring studies are executed efficiently, compliantly, on schedule, and within budget while generating high-quality clinical evidence that supports regulatory and business objectives.
The Director, Clinical Affairs will serve as a key cross-functional leader and liaison among Clinical Affairs, Clinical Research, Regulatory Affairs, Quality, Product Development, and external partners. This individual will provide leadership across clinical operations, including sponsor oversight, site management, CRO and vendor management, clinical data quality, study execution, and evidence generation.
This position reports to the Senior Vice President, Clinical & Regulatory Affairs.
This is a full-time, hybrid position that is located at our Pleasanton headquarters.
Responsibilities:
  • Lead the planning, execution, and oversight of medical device clinical studies from study start-up through close-out
  • Contribute to clinical development strategies supporting product development, regulatory submissions, reimbursement initiatives, commercialization, and post-market evidence generation
  • Provide effective sponsor oversight of clinical trials, including monitoring activities, site performance, protocol compliance, enrollment, and clinical data quality
  • Ensure clinical studies are conducted in accordance with applicable FDA requirements, Good Clinical Practice (GCP), ISO 14155, approved protocols, and company procedures
  • Develop and manage study timelines, budgets, resource plans, enrollment forecasts, and key milestones
  • Proactively identify clinical program risks, develop mitigation strategies, and resolve operational challenges that could impact study timelines, quality, or budget
  • Lead clinical site identification, selection, initiation, engagement, performance management, and close-out activities
  • Build and maintain productive relationships with investigators, study coordinators, research institutions, and other clinical partners
  • Select, manage, and oversee CROs, clinical vendors, consultants, and service providers to ensure quality, timeline, and budget expectations are achieved
  • Support the development and review of clinical study protocols, informed consent forms, case report forms, clinical reports, and other study documentation
  • Partner with Regulatory Affairs to support regulatory submissions requiring clinical evidence and ensure clinical programs are aligned with regulatory strategy
  • Ensure the integrity, completeness, quality, and traceability of clinical data and study documentation
  • Support adverse event review, safety monitoring, clinical risk management, audits, regulatory inspections, and applicable Quality System activities
  • Collaborate with Product Development, Quality, Regulatory Affairs, and Clinical Research to incorporate clinical insights into product development, risk management, labeling, and post-market activities
  • Support the generation of clinical evidence for reimbursement, payer engagement, market access, and commercialization initiatives
  • Establish and monitor clinical program KPIs, study performance metrics, and operational dashboards
  • Provide executive leadership with regular updates regarding study progress, enrollment, budgets, risks, clinical evidence generation, and key program milestones
  • Lead, mentor, and develop Clinical Affairs personnel while establishing clear performance expectations and promoting operational excellence
  • Identify and implement opportunities to improve clinical processes, systems, vendor management, and study execution as the organization scales

Requirements:
  • Bachelor's degree in Nursing, Life Sciences, Biomedical Engineering, or a related scientific or technical discipline
  • Minimum of 8 years of clinical affairs or clinical research experience within the medical device industry
  • Demonstrated leadership experience managing Clinical Affairs personnel, CROs, clinical vendors, and external partners
  • Proven experience managing medical device clinical programs from study start-up through execution and close-out
  • Experience with multiple clinical study models, including multicenter, decentralized, and hybrid clinical trials
  • Strong knowledge of FDA clinical trial requirements, Good Clinical Practice (ICH-GCP), ISO 14155, and applicable clinical research regulations
  • Demonstrated experience providing sponsor oversight of medical device clinical studies
  • Experience developing and managing clinical study budgets, timelines, enrollment forecasts, resources, and operational plans
  • Experience supporting clinical evidence generation for regulatory submissions
  • Strong understanding of clinical study documentation, data quality, safety reporting, monitoring, and inspection-readiness requirements
  • Proven ability to identify and mitigate clinical program risks while managing multiple priorities and studies simultaneously
  • Excellent leadership, project management, organizational, and problem-solving capabilities
  • Strong written and verbal communication skills with the ability to communicate clinical strategy, study performance, and risks to executive leadership
  • Demonstrated ability to effectively collaborate across Clinical Research, Regulatory Affairs, Quality, Product Development, and other functions

Preferred Qualifications:
  • Master's degree or other advanced degree in a relevant scientific, clinical, or technical discipline
  • Experience within a startup or growth-stage medical device organization
  • Experience supporting pivotal or other clinical studies used for FDA submissions and product approvals/clearances
  • Experience generating clinical evidence to support reimbursement, payer coverage, or market access initiatives
  • Experience with neurological, neuromodulation, wearable, or connected medical devices
  • Experience supporting FDA inspections, clinical site audits, and other regulatory or Quality System inspections
  • Experience building or scaling Clinical Affairs functions, processes, and teams
  • Experience working with international clinical studies and regulatory requirements

Compensation:
  • Base Pay: $240,000-$280,000 per year
  • Annual Bonus Eligibility

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