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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 ...

WHOOP

Director, Clinical Operations

Boston, MA · On-site

$210 - $230/hr

As the Director, Clinical Operations, you will lead the clinical operations function responsible ... and medical device clinical research requirements. * Excellent written and verbal communication ...

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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 26, 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.

Senior Clinical Research Associate - Cardiovascular Medical Device

T45 Labs

New York, NY • On-site, Remote

Full-time

Posted 8 days ago

Job description

Senior Clinical Research Associate - Cardiovascular Medical Device
Status: Full-time, Exempt
Reports to: Senior Clinical Operations Manager
Location: Remote
Overview
VahatiCor is an early-stage cardiovascular medical device company developing break through cardiovascular technologies, including Class III catheter-based systems. We operate with a purpose-driven, agile, and collaborative culture, where each team member plays a meaningful role in advancing solutions that improve patient outcomes. As our clinical program grows, we are building a dedicated clinical operations team to support early feasibility studies and future pivotal trials.
The Senior Clinical Research Associate (CRA) will own site activation, clinical study startup, site management, enrollment performance, and protocol execution across VahatiCor's cardiovascular medical device clinical trials. This role serves as the primary operational partner to clinical sites, driving site readiness, investigator engagement, enrollment success, and consistent protocol execution throughout the study lifecycle. The ideal candidate brings deep experience in sponsor-side medical device clinical research, clinical operations, site management, and early-stage medical device clinical trials.
Responsibilities
Site Activation & Study Startup
  • Lead site qualification, feasibility, and readiness activities for assigned cardiovascular medical device clinical trial sites.
  • Own clinical study startup and site activation activities, including collection and review of essential regulatory and startup documentation.
  • Ensure investigators, study coordinators, and site personnel are prepared to enroll patients efficiently and compliantly.
  • Partner with the Clinical Trials Manager and study leadership on site contracting and budgeting activities and ensure timely site activation.
  • Track startup milestones and proactively identify and resolve activation barriers.

Site Management & Enrollment
  • Serve as the primary operational contact for assigned cardiovascular clinical trial sites
  • Build and maintain strong relationships with investigators, coordinators, and site personnel.
  • Drive patient screening and enrollment activities to achieve study recruitment goals.
  • Own site performance across assigned sites and implement actions to improve enrollment, protocol adherence, and study execution.
  • Partner with sites to address operational challenges and maintain study momentum.

Training & Clinical Study Execution
  • Conduct Site Initiation Visits (SIVs) and provide study-specific training to investigators and site personnel.
  • Deliver ongoing site education throughout study execution.
  • Ensure cardiovascular medical device clinical study activities are conducted in accordance with the protocol, Good Clinical Practice (GCP), applicable FDA medical device regulations, and company procedures.
  • Participate in investigator meetings, study team meetings, and site training activities.

Clinical Trial Monitoring & Quality
  • Conduct clinical trial monitoring activities as required to ensure study quality, compliance, and protocol adherence.
  • Review site documentation and study records for completeness and accuracy.
  • Identify protocol deviations, compliance concerns, and operational risks and escalate appropriately.
  • Ensure site documentation is complete, accurate, maintained in accordance with study requirements, and inspection-ready at all times.

Cross-Functional Collaboration
  • Partner cross-functionally with Clinical Operations, Clinical Affairs, Regulatory, and Quality to support effective study execution.
  • Communicate site feedback, enrollment trends, operational challenges, and emerging risks to study leadership.
  • Contribute to continuous improvement of site activation, enrollment, and study execution processes.

Required Experience & Qualifications
  • Bachelor's degree in Life Sciences, Nursing, Biomedical Engineering, or a related scientific discipline.
  • 7+ years of clinical research experience supporting medical device clinical trials.
  • Sponsor-side medical device clinical research experience is required. Candidates whose experience is primarily CRO-based without direct sponsor-side medical device experience will not meet the requirements for this role.
  • Prior clinical operations experience within an early-stage medical device company is required.
  • Demonstrated experience owning clinical study startup, site activation, patient enrollment, and clinical trial execution activities.
  • Experience owning site qualification, Site Initiation Visits (SIVs), clinical trial monitoring, and site management activities.
  • Cardiovascular medical device clinical trial experience is highly valued, particularly experience with catheter-based or other interventional cardiovascular technologies.
  • Demonstrated understanding of Good Clinical Practice (GCP), FDA medical device regulations, and clinical research operations.
  • Strong written and verbal communication skills.
  • Strong organizational, relationship-building, and problem-solving skills.
  • Ability and willingness to travel up to 60% to conduct site startup, activation, training, monitoring, and study execution activities.
  • Thrives in a dynamic, fast-paced, early-stage medical device environment where adaptability, initiative, and collaboration are critical to success.

Why Work for VahatiCor?
  • Help bring a first-of-its-kind therapy to patients with coronary microvascular dysfunction, a large and historically underserved patient population with limited treatment options.
  • Work alongside an experienced leadership team with deep expertise in cardiovascular medical devices, clinical research, regulatory affairs, and commercialization.
  • Make a visible impact in a collaborative, fast-moving environment where individual contributions directly influence the future of the technology, the clinical program, and the company.

Eligibility
Candidates must be permanently authorized to work in the United States without the need for current or future visa sponsorship. We are currently unable to sponsor employment visas or permanent residency (PERM) applications.
Location and Compensation
This is a remote position supporting clinical sites throughout the Eastern United States. We are prioritizing candidates who reside in the Eastern or Central time zone and are located within reasonable proximity to a major airport to support travel requirements. Travel of up to 60% is required based on study and site needs.
The anticipated annual base salary range for this position is $113,000 - $153,000. Actual compensation will be determined based on experience, qualifications, geographic location, and other job-related factors. VahatiCor is committed to fair and equitable pay practices. In addition to base salary, the total compensation package may include bonus opportunities, equity, and company-sponsored benefits.
Equal Opportunity Statement
VahatiCor is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Employment decisions are based on qualifications, merit, and business needs. We do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic.
Third-Party Recruiter Notice
We do not accept unsolicited resumes from staffing agencies or recruiters without a signed agreement in place. Any resumes submitted without such an agreement will be considered the property of VahatiCor and no fees will be paid if the candidate is hired. Agencies interested in submitting candidates may email careers@t45labs.com.

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