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Clinical Research - Medical Assistant

Layton, UT · On-site

$25 - $34/hr

Clinical Research Coordinator (CRC I) - Pediatric & Vaccine Studies Layton & Murray, Utah $25.00 ... Our positions are not temporary or contract, they are direct hire with full benefits. Our purpose ...

Actalent

Clinical Research Coordinator

San Antonio, TX · On-site

$23 - $28/hr

Clinical Research Coordinator This role coordinates and manages all aspects of clinical research ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

Actalent

Clinical Research Coordinator

Norfolk, NE

$25 - $33/hr

Job Title: Part-Time Clinical Research Coordinator Hours: 20 per week (flexible Monday-Friday ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

Actalent

Clinical Research Coordinator

Norfolk, VA · On-site

$25 - $35/hr

Clinical Research Coordinator (Cardiology) - Norfolk, VA Start Date: ASAP This role provides ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

Mayo Clinic

Clinical Research Coordinator

Rochester, MN · On-site

$24.75 - $32.75/hr

As a Clinical Research Coordinator, you will have the opportunity to work with a variety of people ... Positions may vary in FTE, from supplemental to full-time. Some positions may also be temporary ...

Mayo Clinic

Clinical Research Coordinator

Rochester, MN · On-site

$27.99 - $41.98/hr

Positions may vary in FTE, from supplemental to full-time. Some positions may also be temporary ... As a Clinical Research Coordinator, you will: * Independently coordinate complex (i.e ...

Actalent

Clinical Research Coordinator

Chandler, AZ · On-site

$27 - $36/hr

Clinical Research Coordinator II / III Location: Peoria, AZ Schedule: Full-time Position Summary We ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

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Temporary Clinical Research information

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$12

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How much do temporary clinical research jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for temporary clinical research in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

How much does a CRC make?

A Clinical Research Coordinator (CRC) in Houston typically earns between $50,000 and $70,000 annually, depending on experience, certifications, and the complexity of the trials. Entry-level CRCs may start at lower salaries, while experienced coordinators with certifications like CCRP can earn higher wages. Salaries may also vary based on the employer and workload.

Can you be a CRA with no experience?

Becoming a Clinical Research Associate (CRA) typically requires some background in healthcare, life sciences, or related fields, along with knowledge of Good Clinical Practice (GCP) guidelines. While entry-level CRA positions may be available, most employers prefer candidates with prior experience in clinical trials or related roles, and some may offer training programs for newcomers. Certification and familiarity with clinical trial management systems can also improve job prospects for those with limited experience.

What are the key skills and qualifications needed to thrive in the Temporary Clinical Research position, and why are they important?

To excel in Temporary Clinical Research, candidates typically need a background in life sciences or healthcare, familiarity with clinical trial protocols, and attention to regulatory compliance. Experience with data collection software, electronic data capture (EDC) systems, and Good Clinical Practice (GCP) certification are highly valuable. Strong organizational, communication, and problem-solving skills help professionals adapt quickly and contribute effectively in temporary project-based settings. These abilities ensure accurate, ethical research conduct and seamless integration with research teams, even on short-term assignments.

What is a Temporary Clinical Research job?

A Temporary Clinical Research job involves assisting in medical or scientific studies for a limited period. Responsibilities may include data collection, patient interaction, regulatory compliance, and administrative support. These roles are often project-based and may be available in hospitals, universities, or pharmaceutical companies. Temporary positions allow professionals to gain experience in clinical research without committing to a long-term role.

Is it hard to get a CRA job?

Securing a Clinical Research Associate (CRA) position can be competitive, often requiring relevant experience, a degree in life sciences or related fields, and knowledge of Good Clinical Practice (GCP) guidelines. Entry-level roles may be easier to obtain with strong educational backgrounds and certifications like the CCRP, but advancing to more senior CRA positions typically demands proven experience in clinical trial monitoring. The hiring process often involves interviews, background checks, and demonstrating familiarity with clinical trial management tools.

Which is better, CRC or CRA?

A Clinical Research Coordinator (CRC) manages daily trial activities at the site level, including patient interactions and data collection, while a Clinical Research Associate (CRA) monitors multiple sites to ensure protocol compliance and data integrity. Both roles require knowledge of Good Clinical Practice (GCP) and relevant certifications, but CRCs typically work on-site, and CRAs often travel to monitor sites remotely or in person. The choice depends on whether you prefer hands-on site management or overseeing multiple sites from a monitoring perspective.

What are the typical responsibilities of someone working in a Temporary Clinical Research position?

In a Temporary Clinical Research role, you can expect to assist with tasks such as collecting and managing study data, coordinating participant visits, and ensuring compliance with study protocols. You may also help with regulatory documentation, support the recruitment of research subjects, and collaborate closely with investigators, sponsors, and other research team members. Since these positions are project-based, you’ll need to adapt quickly to new environments and processes. This role provides valuable hands-on experience in clinical research, and can be a great stepping stone for those aiming to advance to permanent or higher-level positions in the field.

More about Temporary Clinical Research jobs
What cities are hiring for Temporary Clinical Research jobs? Cities with the most Temporary Clinical Research job openings:
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Temporary Clinical Research jobs near you
Clinical Research Technician (Temporary)

Clinical Research Technician (Temporary)

University of Michigan

Ann Arbor, MI • On-site

Full-time

Medical, Dental, Vision, Retirement

Posted 4 days ago

University Of Michigan rating

8.1

Company rating: 8.1 out of 10

Based on 140 frontline employees who took The Breakroom Quiz

131st of 535 rated colleges and universities

Job description

How to Apply
A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.
Mission Statement
Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. Our mission is guided by our Strategic Principles and has three critical components; patient care, education and research that together enhance our contribution to society.
Job Summary
The Clinical Research Technician will support coordination and implementation of ongoing clinical research studies focused on hypertension treatment and stroke prevention. Responsibilities include participant recruitment, screening, enrollment, scheduling study visits, participant follow up, and maintenance of study documentation.
Responsibilities*
  • Coordinate day-to-day activities for assigned clinical research studies
  • Recruit, screen, and enroll study participants in accordance with protocol requirements
  • Schedule and manage study visits, including follow-up activities
  • Serve as a primary point of contact for study participants, ensuring clear communication and positive participant experience
  • Maintain accurate and timely study documentation, including regulatory and source documents
  • Assist with data collection and entry in study databases
  • Support study teams and investigators with operational tasks related to study execution
  • Collaborate with research staff and leadership to ensure adherence to study timelines and goals

Required Qualifications*
  • Associate degree in Health Science or an equivalent combination of related education and experience is necessary.
  • Minimum 1 year of directly related experience in clinical research and clinical trials is necessary. (Please review SoCRA?s Definition of a Clinical Research Professional for qualifying experience prior to applying.)

or
An advanced degree in a health-related areas such as: Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD.
or
Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research.
Desired Qualifications*
  • Bachelor's degree in health sciences, public health, or related field, or equivalent combination of education and experience
  • Strong organizational, communication, and interpersonal skills
  • Ability to manage multiple tasks and priorities in a fast-paced research environment
  • Experience interacting with human subjects or working in a clinical or research setting is preferred
  • Prior experience coordinating clinical research studies
  • Familiarity with participant recruitment and retention strategies
  • Experience with data entry and research documentation systems (e.g., REDCap)

Why Join Michigan Medicine?
Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in 1850. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world's most distinguished academic health systems. In some way, great or small, every person here helps to advance this world-class institution. Work at Michigan Medicine and become a victor for the greater good.
What Benefits can you Look Forward to?
  • Excellent medical, dental and vision coverage effective on your very first day
  • 2:1 Match on retirement savings

Modes of Work
Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes .
Work Locations
Hurley Hospital, Flint, MI
Underfill Statement
This position may be underfilled at a lower classification depending on the qualifications of the selected candidate.
Additional Information
Work environment: This position works closely with a multidisciplinary research team and requires frequent interaction with study participants. The role may involve a combination of on-site and remote work, depending on study needs.
Appointment Type: Full-Time, Term-Limited (1 year, with potential for extension based on funding)
Application Deadline
Job openings are posted for a minimum of seven calendar days. The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled any time after the minimum posting period has ended.
U-M EEO Statement
The University of Michigan is an equal employment opportunity employer.
Job Detail
Job Opening ID
278576
Working Title
Clinical Research Technician (Temporary)
Job Title
Clinical Research Technician
Work Location
Ann Arbor Campus
Ann Arbor, MI
Modes of Work
Onsite
Full/Part Time
Full-Time
Regular/Temporary
Regular
FLSA Status
Nonexempt
Organizational Group
Medical School
Department
MM Emergency Medicine UM Adult
Posting Begin/End Date
6/08/2026 - 6/15/2026
Career Interest
Research
Temporary Job Opening

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About University of Michigan

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The University of Michigan (U-M), based in Ann Arbor, MI, US, is one of America's most esteemed institutions in higher education. Established in 1817, it presides in the industry of education and research, providing a range of services including undergraduate, graduate, and professional education programs. Complementing this is an extensive research activity that has significantly contributed to various fields, from healthcare to engineering, humanities to sports. Upholding its mission "to serve the people of Michigan and the world through preeminence in creating, communicating, preserving and applying knowledge, art, and academic values", U-M consistently ranks among the top universities globally, a testament to its tradition of excellence in learning and research, and a deep commitment to innovation and discovery.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Ann Arbor, MI, US

Year founded

1817

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