1

Clinical Research Trainee Jobs (NOW HIRING)

Clinical Research Coordinator

Madison, WI · On-site

$24.50 - $32.50/hr

... trainees. The Department of Radiation Medicine currently houses 45 faculty members: 18 clinical radiation oncologists (five MD/PhD physician-scientists leading laboratory research programs), 18 ...

Provide guidance and operational training to junior staff, trainees, students, and temporary personnel as requested by the Government. * Coordinate multiple clinical research studies simultaneously ...

Provide guidance and operational training to junior staff, trainees, students, and temporary personnel as requested by the Government. * Coordinate multiple clinical research studies simultaneously ...

Clinical Research Coordinator

Ithaca, NY · On-site

$24 - $31.75/hr

... trainees. The successful candidate will serve as an integral part of this research team. Required ... Clinical database management experience (i.e. REDCap) and proficiency with statistical software (i ...

Clinical Research Coordinator II Job Summary: The Department of Orthopedics & Rehabilitation is ... The coordinator will work closely with the sports medicine clinic staff, students, and trainees to ...

Responsible for all other activities, clinical and administrative, as needed. * Provides technical direction to research staff. * Operates with direct guidance and work assignments are generally ...

Responsible for all other activities, clinical and administrative, as needed. * Provides technical direction to research staff. * Operates with direct guidance and work assignments are generally ...

Showing results 21-40

Clinical Research Trainee information

See salary details

$9

$31

$68

How much do clinical research trainee jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for clinical research trainee in the United States is $31.53, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $39.18 per hour, depending on experience, location, and employer.

What is a clinical research trainee?

Clinical Research Trainees are individuals, often students or recent graduates, who are gaining practical experience in the field of clinical research. They assist in the design, implementation, and monitoring of clinical trials under the supervision of experienced researchers. Their responsibilities may include data collection, managing study documentation, ensuring compliance with regulatory guidelines, and supporting patient recruitment. The role provides foundational knowledge and hands-on skills necessary for a career in clinical research or related healthcare fields.

What are the typical responsibilities of a clinical research trainee during a clinical trial?

As a Clinical Research Trainee, you will typically assist with the coordination and execution of clinical trials under the supervision of experienced research staff. Your daily tasks may include collecting and managing patient data, assisting with patient recruitment and informed consent, preparing study documentation, and ensuring compliance with regulatory guidelines. Trainees often collaborate closely with clinical teams, principal investigators, and external partners, gaining hands-on experience across various study phases. This role provides valuable exposure to clinical research protocols and is a great foundation for advancing into more senior research or coordinator positions.

What are the key skills and qualifications needed to thrive as a clinical research trainee, and why are they important?

To thrive as a Clinical Research Trainee, you need a solid background in life sciences or healthcare, attention to detail, and a foundational understanding of research methodologies, typically supported by a relevant degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and clinical trial management software is essential. Strong organizational skills, effective communication, and the ability to collaborate within multidisciplinary teams are standout soft skills. These competencies ensure that clinical trials are conducted ethically, efficiently, and in compliance with regulatory standards.

What is the difference between Clinical Research Trainee vs Clinical Research Coordinator?

AspectClinical Research TraineeClinical Research Coordinator
Required CredentialsTypically pursuing or holding a relevant degree (e.g., life sciences, healthcare)Usually has a degree or certification in clinical research or related field
Work EnvironmentTraining setting, often in academic or research institutionsActive role in managing clinical trials at research sites or hospitals
Employer & Industry UsageEducational programs, research institutions, pharmaceutical companiesHospitals, clinics, research organizations
Common Search & Comparison IntentUnderstanding entry-level roles and training opportunitiesClarifying responsibilities and career progression in clinical research

While both roles are involved in clinical research, a Clinical Research Trainee is typically in a learning or internship phase, gaining foundational knowledge. In contrast, a Clinical Research Coordinator actively manages and oversees clinical trials, requiring more experience and responsibility.

More about Clinical Research Trainee jobs

What cities are hiring for Clinical Research Trainee jobs?

Cities with the most Clinical Research Trainee job openings:

What are the most commonly searched types of Clinical Research jobs?

The most popular types of Clinical Research jobs are:

What states have the most Clinical Research Trainee jobs?

States with the most job openings for Clinical Research Trainee jobs include:

Infographic showing various Clinical Research Trainee job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $65,588 per year, or $31.5 per hour.

Clinical Research Coordinator

University of Wisconsin-Madison

Madison, WI • On-site, Remote

$24.50 - $32.50/hr

Full-time

Medical, Retirement, PTO

Re-posted 24 days ago


University Of Wisconsin-Madison rating

8.3

Company rating: 8.3 out of 10

Based on 56 frontline employees who took The Breakroom Quiz

126th of 619 rated colleges and universities


Job description

Current Employees: If you are currently employed at any of the Universities of Wisconsin, log in to Workday to apply through the internal application process.
Job Category:
Academic Staff
Employment Type:
Regular
Job Profile:
Clinical Research Coordinator I
Job Summary:
The Department of Radiation Medicine at the University of Wisconsin-Madison in the School of Medicine and Public Health (SMPH) is seeking a motivated and detail oriented Clinical Research Coordinator I or II to join a dynamic and collaborative research team. In this role, you will coordinate industry sponsored and internally funded prospective clinical trials across multiple investigators, contributing directly to research that advances patient care and medical innovation.
You will work closely with the Radiation Medicine Clinical Research Coordinator team, Program Manager, and a multidisciplinary team of investigators and clinical partners on exciting studies. This position offers hands on involvement in impactful clinical research and the opportunity to build strong professional expertise in a nationally recognized academic medical environment.
The ideal candidate thrives in a fast paced, complex setting, enjoys managing multiple priorities, and is committed to maintaining high standards of patient care, regulatory compliance, and professionalism. The Department of Radiation Medicine is a national leader in clinical care, research, and education, providing an excellent environment for career development, mentorship, and meaningful contribution to cutting edge clinical research.
  • Applicants for this position will be considered for the following titles: Clinical Research Coordinator I, Clinical Research Coordinator II. The title is determined by the experience and qualifications of the finalist.
  • This position has been identified as a position of trust with access to vulnerable populations. The selected candidate will be required to pass an initial caregiver check to be eligible for employment under the Wisconsin Caregiver Law and every four years.

Key Job Responsibilities:
  • Manages research workflow components, collects, prepares, processes, and submits participant data and samples to appropriate entities, adhering to research protocols
  • Recruits, screens, selects, determines eligibility and enrolls trial participants, collects more complex information, performs medical assessments, and answers varied questions under supervision of a medically licensed professional. Performs medical assessments after completion of required training/certification, such as collecting vital signs, obtaining weight, and performing phlebotomy
  • May assist with training of staff
  • Schedules logistics, determines workflows, and secures resources for clinical research trials
  • Identifies work unit resources needs and manages supply and equipment inventory levels
  • Performs quality checks
  • Serves as a main point of contact for clinical research participants, providing information regarding research procedures, expectations, and informational inquiries. Ensures participants follow the research protocol and alerts Principal Investigator of issues
  • Identifies resource needs and develops clinical research documents, such as job aids, tools, processes, procedures, and training. Contributes to the development of protocols

Department:
School of Medicine and Public Health, Radiation Medicine
The Department of Radiation Medicine (DRM) was established in 1975, bringing together physicians and scientists from radiation oncology, medical oncology and cancer biology whose academic activities include clinical cancer care, clinical and laboratory research and education. Highly regarded as a clinical and research powerhouse, the productivity of the department is paired with a vibrant culture that fosters respect, mutual support and well-being. The department serves as the cornerstone of the renowned UW Carbone Cancer Center, which received National Cancer Institute designation in 1973 as one of the first six Comprehensive Cancer Centers in the United States.
The department's setting within a top-tier university and the nation's first School of Medicine and Public Health is key to success. Bridging research faculty and clinicians from many areas of cancer treatment, the department is focused on three primary areas: clinical radiation oncology, radiation oncology physics and cancer biology. These three groups work to ensure delivery of the highest quality clinical care for cancer patients, foster innovative clinical and translational research and provide a rich educational environment for radiation oncology and radiation oncology physics residents, medical students, graduate students and other trainees.
The Department of Radiation Medicine currently houses 45 faculty members: 18 clinical radiation oncologists (five MD/PhD physician-scientists leading laboratory research programs), 18 radiation oncology physicists, four PhD cancer biologists and five emeritus professors. Growth over the last decade has more than doubled the size of the faculty and tripled the total research funding. The department's leadership structure is dedicated to supporting a diverse workplace and promoting an environment of equity for all faculty, staff, learners and patients.
Compensation:
The starting salary for the position is $55,000; but is negotiable based on experience and qualifications.
Employees in this position can expect to receive benefits such as generous vacation, holidays, and sick leave; competitive insurances and savings accounts; retirement benefits. For more information, refer to the campus benefits webpage and the SMPH Academic Staff Benefits Flyer
Required Qualifications:
  • Prior work experience in a health care setting or with human patients
  • Prior work experience with electronic medical/health records (EMR or EHR) systems

Preferred Qualifications:
  • Previous experience coordinating clinical trials
  • Prior experience adhering to IRB approved protocols
  • Prior experience with FDA regulated clinical trials
  • Prior experience with electronic data capturing (EDC

Education:
  • Preferred Bachelor's Degree with focus in biological or health sciences, health care or related field

How to Apply:
For the best experience completing your application, we recommend using Chrome or Firefox as your web browser.
To apply for this position, select either "I am a current employee" or "I am not a current employee" under Apply Now. You will then be prompted to upload your application materials.
Important: The application has only one attachment field. Upload the following documents in that field, either as a single combined file or as multiple files in the same upload area. Failure to submit the required documents will result in no longer being considered for the position.
• Cover letter - required
• Resume - required
Your cover letter should address how your training and experience aligns with the required and preferred qualifications listed above. Application reviewers will rely on these written materials to determine which applicants move forward in the process. References will be requested from final candidates. All applicants will be notified once the search concludes and a candidate is selected
University sponsorship is not available for this position, including transfers of sponsorship and TN visas. The selected applicant will be responsible for ensuring their continuous eligibility to work in the United States (i.e. a citizen or national of the United States, a lawful permanent resident, a foreign national authorized to work in the United States without the need of an employer sponsorship) on or before the effective date of appointment. This position is an ongoing position that will require continuous work eligibility. If you are selected for this position you must provide proof of work authorization and eligibility to work.
Contact Information:
Kirsten Gragg, kgragg@wisc.edu, 608-265-3357. Relay Access (WTRS): 7-1-1. See RELAY_SERVICE for further information.
Institutional Statement on Diversity:
Diversity is a source of strength, creativity, and innovation for UW-Madison. We value the contributions of each person and respect the profound ways their identity, culture, background, experience, status, abilities, and opinion enrich the university community. We commit ourselves to the pursuit of excellence in teaching, research, outreach, and diversity as inextricably linked goals.
The University of Wisconsin-Madison fulfills its public mission by creating a welcoming and inclusive community for people from every background - people who as students, faculty, and staff serve Wisconsin and the world.
The University of Wisconsin-Madison is an Equal Opportunity Employer.
Qualified applicants will receive consideration for employment without regard to, including but not limited to, race, color, religion, sex, sexual orientation, national origin, age, pregnancy, disability, or status as a protected veteran and other bases as defined by federal regulations and UW System policies. We promote excellence by acknowledging skills and expertise from all backgrounds and encourage all qualified individuals to apply. For more information regarding applicant and employee rights and to view federal and state required postings, visit the Human Resources Workplace Poster website.
To request a disability or pregnancy-related accommodation for any step in the hiring process (e.g., application, interview, pre-employment testing, etc.), please contact the Divisional Disability Representative (DDR) in the division you are applying to. Please make your request as soon as possible to help the university respond most effectively to you.
Employment may require a criminal background check. It may also require your references to answer questions regarding misconduct, including sexual violence and sexual harassment.
The University of Wisconsin System will not reveal the identities of applicants who request confidentiality in writing, except that the identity of the successful candidate will be released. See Wis. Stat. sec. 19.36(7).
The Annual Security and Fire Safety Report contains current campus safety and disciplinary policies, crime statistics for the previous 3 calendar years, and on-campus student housing fire safety policies and fire statistics for the previous 3 calendar years. UW-Madison will provide a paper copy upon request; please contact the University of Wisconsin Police Department.

What University Of Wisconsin-Madison employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


University of Wisconsin logo

About University of Wisconsin

Sourced by ZipRecruiter

The University of Wisconsin, based in Madison, WI, US, functions in the educational industry and is a renowned and respected institution for higher education. Its official website is wisc.edu. Established in 1848, this public research university is recognized globally for its innovative approach to education, research, creativity, and public service. It embodies a strong commitment to academic freedom and academic excellence. As a major contributor to the Wisconsin Idea, it aims to accomplish its mission of generating well-rounded individuals who will contribute substantially to society, the local community, and the global economy.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Madison, WI, US

Year founded

2005