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Part Time Medical Device Clinical Research Jobs (NOW HIRING)

IQVIA

Clinical Research Coordinator

Sioux Falls, SD · On-site

$35 - $42/hr

We partner with top pharmaceutical, biotechnology, and medical device companies to accelerate ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Research Coordinator

Wichita, KS

$35 - $42/hr

We partner with leading pharmaceutical, biotechnology, and medical device organizations to improve ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Research Coordinator

Union, SC · On-site

$35 - $42/hr

We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Research Coordinator

Jefferson City, MO

$35 - $42/hr

We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Research Coordinator

Albuquerque, NM

$35 - $42/hr

We collaborate with leading pharmaceutical, biotechnology, and medical device organizations to ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

We partner with the world's leading pharmaceutical, biotechnology, and medical device organizations ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

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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 Aug 23, 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?

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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 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 $107,336 per year, or $51.6 per hour.

Sr Clinical Research Associate-Class III Device

Kelly Services

Minneapolis, MN

$110K/yr

Full-time, Part-time, Contractor

Medical, Dental, Vision, Life, Retirement

Posted 13 days ago

Job description

Title: Senior Clinical Research Associate-Medical Device

Pay: Starting at $110,000, DOE

FT or PT: Full-time, Contract-to-hire (about 3 months to conversion)

Location: Remote with domestic travel (25-50% anticipated)

Kelly® Science & Clinical is seeking a Senior Clinical Research Associate for a temp-to-hire position at an early-stage, innovation-driven medical device client. If you’re passionate about supporting high-impact clinical studies and improving patient care in surgical settings, and are ready to take the next step in your career, trust The Experts at Hiring Experts.

As a Senior Clinical Research Associate, you will be responsible for overseeing the execution of clinical trials from site start-up to site closure, ensuring compliance with study protocols, regulatory requirements, and maintaining quality documentation. Key responsibilities include coordinating and conducting site qualification, initiation, and monitoring visits; managing site operations; reviewing informed consent procedures; assessing investigational product accountability; and supporting the development of study documentation and site-facing presentation materials. You will develop strong relationships with clinical site staff, proactively identify and mitigate risks, and facilitate timely communication among stakeholders.

Requirements:

  • Bachelor’s Degree or higher in healthcare or science related field (alternately, relevant experience may be considered)
  • Minimum 5 years’ experience as a Clinical Research Associate
  • At least 3 years of monitoring Class III medical device trials
  • Proficiency with Epic required
  • Thorough knowledge of clinical research concepts, FDA regulations, and Good Clinical Practice (GCP)
  • Strong organizational, communication, and critical thinking skills
  • Willingness and ability to travel domestically 25-50% of the time
  • Experience in breast cancer, breast reconstruction, or related therapeutic areas preferred
  • Proficient in Microsoft Office and comfortable learning new clinical trial management systems

Our client offers a fast-paced, high-growth environment with opportunities for professional development and impactful work. If you have a passion for clinical research and medical devices, apply today!


As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.