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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

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

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

Albuquerque, NM · On-site

$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 - Union, SC

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 ...

Main Line Health

Clinical Research Coord II

Wynnewood, PA · On-site

$23.25 - $31/hr

The Clinical Research Coordinator will manage a variety of device trials and support Phase II-IV ... This position is eligible for up to $6,000 per year based upon your Full or Part Time status.

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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 Sep 13, 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:

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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 September 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Study Manager Medical Device

Plano, TX • On-site

Kelly Services
See more jobs at Kelly Servicesexternal

$134K - $145K/yr

Full-time, Part-time

Medical, Dental, Vision, Life, Retirement

This job post has expired today. Applications are no longer accepted.

Job description

Clinical Study Manager
  • Pay: $134,000-$145,000
  • FT or PT: Full-Time
  • Location: Plano, Texas (Hybrid)

Kelly® Science & Clinical is seeking a Clinical Study Manager for a direct-hire position at our innovative medical device client. If you’re passionate about leading clinical investigations for novel medical technologies and ready to take the next step in your career, trust The Experts at Hiring Experts.

As the Clinical Study Manager, you will lead the planning, execution, and oversight of clinical studies spanning the full medical device product lifecycle, including premarket and postmarket initiatives. This high-impact role ensures studies are conducted in alignment with ISO 14155, FDA regulations, EU MDR, and Good Clinical Practice (GCP). You will serve as the primary operational lead for assigned research projects, managing study timelines, budgets, site performance, vendor relationships, and data integrity. You’ll collaborate cross-functionally with Regulatory Affairs, Quality, Medical Affairs, and Product Development teams to support robust clinical evidence generation.

Key Responsibilities:

  • Lead and coordinate all aspects of clinical research, from study start-up to closeout (IDE, post-market, PMCF, registries, and observational studies)
  • Develop and manage project plans, study timelines, milestones, and budgets
  • Oversee clinical study documentation including protocols, informed consent forms, CRFs, statistical plans, and agreements
  • Manage site selection, qualification, initiation, monitoring, and performance oversight
  • Ensure compliance with regulatory and GCP requirements, supporting audits and inspections
  • Supervise vendors (CROs, labs) and monitor resource allocation and expenditures
  • Guide Clinical Research Associates and study team members with operational leadership
  • Drive risk management, data quality, and continuous process improvement

Requirements:

  • Bachelor’s degree in Life Sciences, Engineering, or related field; Master’s or PhD preferred
  • 3–8+ years of clinical research experience, including 2+ years in medical device study management
  • Strong knowledge of ISO 14155, FDA regulations, EU MDR, and GCP
  • Experience with EDC, CTMS, and eTMF systems
  • Exceptional project management, organizational, and communication skills
  • Certification (ACRP, SOCRA) and experience with interventional/procedural studies (IR, vascular, cardiology) preferred
  • Ability to travel up to 40% to clinical sites and industry meetings

Ready to make an impact in medical device innovation? 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.