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Part Time Medical Device Clinical Research Jobs (NOW HIRING)

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Senior Medical Research Associate

Lenexa, KS · On-site

We advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of all ...

ICON

Senior Medical Research Associate

Lenexa, KS · On-site

We advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of all ...

Protouch Staffing

Clinical Research GI

Scottsdale, AZ · On-site

Job Title: Part-Time Clinical Research Gastroenterologist - (Must Own Clinic/Practice) Location ... The physician will provide medical oversight, ensure protocol compliance, monitor participant ...

IQVIA

MedTech Part Time Clinical Consultant

Paducah, KY · On-site

$60/hr

Improve patient outcomes by delivering ventricular medical device education in a variety of ... clinical research services, commercial insights and healthcare intelligence to the life sciences ...

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All JobsMedical Device Clinical Research JobsPart Time JobsPart Time Medical Device Clinical Research Jobs

Part Time Medical Device Clinical Research information

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$49K

$107.3K

$189K

How much do part time medical device clinical research jobs pay per year?

As of Sep 15, 2026, the average yearly pay for part time medical device clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is a part time medical device clinical research?

A part time medical device clinical research job involves supporting clinical trials or studies that evaluate the safety and effectiveness of medical devices, but on a reduced or flexible schedule. Professionals in this role may assist with tasks such as data collection, patient monitoring, regulatory documentation, and coordinating with healthcare teams. These positions are ideal for those seeking work-life balance or who have other commitments, while still contributing to important medical advancements. Part time roles can be found in hospitals, research organizations, or medical device companies.

What are the typical responsibilities of a part time medical device clinical research professional?

In a part-time medical device clinical research role, you will typically assist with study coordination, data collection, and documentation to ensure compliance with regulatory standards. This may involve supporting patient enrollment, monitoring trial progress, and helping to prepare reports or presentations. You will often collaborate closely with clinical research coordinators, investigators, and regulatory teams to ensure the study runs smoothly. The part-time nature of the job can offer flexibility, but it also requires excellent time management to balance multiple tasks and deadlines within limited hours.

What skills and qualifications are needed for a part time medical device clinical research professional?

To thrive in Part Time Medical Device Clinical Research, you need a background in life sciences or healthcare, knowledge of clinical trial protocols, and familiarity with regulatory requirements such as Good Clinical Practice (GCP). Experience with electronic data capture (EDC) systems, clinical trial management software, and possibly certifications like SOCRA or ACRP are highly beneficial. Strong attention to detail, communication skills, and the ability to work both independently and collaboratively make candidates stand out. These competencies are crucial for ensuring compliant, accurate, and efficient clinical research that supports medical device safety and efficacy.

What is the difference between Part Time Medical Device Clinical Research vs Part Time Medical Device Quality Assurance?

AspectPart Time Medical Device Clinical ResearchPart Time Medical Device Quality Assurance
Required CredentialsTypically requires a background in life sciences, clinical research certifications, or related degreesOften requires quality assurance certifications, such as ISO standards or GMP training
Work EnvironmentConducts studies in clinical settings, hospitals, or research facilitiesWorks in manufacturing sites, labs, or compliance departments
Employer & Industry UsageUsed by clinical research organizations, medical device companies, and hospitalsUsed by manufacturing firms, regulatory agencies, and quality departments

Part Time Medical Device Clinical Research focuses on conducting clinical trials and gathering data on medical devices, while Part Time Medical Device Quality Assurance ensures products meet safety and quality standards. Both roles are essential in the medical device industry but serve different functions in the product lifecycle.

More about Part Time Medical Device Clinical Research jobs

What cities are hiring for Part Time Medical Device Clinical Research jobs?

Cities with the most Part Time 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 Part Time Medical Device Clinical Research jobs?

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

What job categories do people searching Part Time Medical Device Clinical Research jobs look for?

The top searched job categories for Part Time Medical Device Clinical Research jobs are:

Part Time Medical Device Clinical Research jobs near you
Infographic showing various Part Time Medical Device Clinical Research job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Physician - Cardiologist (Part time)

Decatur, GA • On-site

Alcanza Clinical Research
51 - 200 employees
Learn more about Alcanza Clinical Researchexternal

Part-time

Medical, Dental, Vision, Life, Retirement

Re-posted 7 days ago

Job description

Clinical Research Physician - Cardiologist (Part time)
Department: Operations
Employment Type: Part Time
Location: Accel Research Sites - Decatur, GA
Reporting To: Adrienne Hilliard
Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site.
Key Responsibilities
Essential Job Duties:
  • Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes
  • Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance
  • Evaluates and assesses participants to ensure only eligible participants enroll into the trials.
  • Participates and engages in successful delivery and retention of study participants.
  • Interacts positively and collaboratively with sponsors, clients and team members.
  • Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs.
  • Actively involved in protocol training for staff.
  • Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues.
  • Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company.

Skills, Knowledge and Expertise
Minimum Qualifications: MD or DO degree, an active physician license (in good standing) in the state of practice for this role is required. Board certification is required.
Required Skills:
  • Clinical skills and clinical procedures based in area of specialty.
  • Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm).
  • Must possess strong organizational skills, attention to detail, and math proficiency.
  • Well-developed written and verbal communication skills. Bi-lingual (English / Spanish) proficiency is highly preferred.
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, employees, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
  • Ability to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.
  • Must possess a high degree of urgency, self-motivation, integrity and dependability.
  • Ability to work independently to identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.

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