Entry Level Clinical Research Associate Jobs
New grad clinical research associate jobs welcome recent graduates and entry level candidates with zero to two years of experience, where strong internship work or hands-on trial coordination can matter more than a long resume. Most openings mix on-site and remote settings across Education, Healthcare & Medical Services, and Biotechnology & Pharmaceuticals, with employers like Medpace, IQVIA, and University of Miami hiring at this level now.
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Department:
Location:
Health Sciences CenterTime Type:
Full timeWorker Type:
RegularJob Req ID:
R109543Minimum Requirements:
High School Diploma/GED and a minimum of two (2) years of relevant experience or an equivalent combination of education and experience. Grade 2 (Hourly)Position Description:
Under the direction of the Principal Investigator(s) in the Department of Surgery, the Clinical Research Coordinator II is responsible for participant recruitment, screening, informed consent, enrollment, and biospecimen collection for multiple clinical research studies. The Clinical Research Coordinator II works collaboratively with investigators, clinical care teams, laboratory personnel, and regulatory staff to ensure protocol compliance, participant safety, and the accurate collection, processing, documentation, and transport of clinical samples to designated research laboratories.
Essential Duties and Responsibilities
- Coordinates participant recruitment, screening, enrollment, and retention for multiple clinical research studies.
- Identifies and approaches potentially eligible participants in inpatient and outpatient clinical settings.
- Obtains informed consent and maintains ongoing communication with study participants throughout their participation.
- Collects, processes, labels, documents, stores, and transports biological specimens according to study protocols, institutional policies, and regulatory requirements.
- Maintains chain-of-custody documentation and ensures timely delivery of research specimens to designated Department of Surgery laboratories.
- Collaborates with investigators, clinical staff, laboratory personnel, and research teams to facilitate study enrollment and sample collection activities.
- Ensures assigned studies are conducted in accordance with University of Louisville Institutional Review Board (IRB) requirements, Good Clinical Practice (GCP) guidelines, applicable federal regulations, and institutional policies.
- Maintains accurate and complete study documentation, source records, participant logs, and specimen tracking records.
- Performs data collection, data entry, and quality assurance activities in accordance with study protocols and established standard operating procedures.
- Assists with preparation and maintenance of regulatory documents, study files, and IRB submissions as needed.
- Communicates study requirements and participant schedules with investigators, research staff, and clinical teams to ensure successful study implementation.
- Supports monitoring visits, audits, and quality assurance activities by maintaining organized and compliant study records.
- Maintains inventory and supplies necessary for participant enrollment, specimen collection, processing, and storage.
Target Compensation Maximum:
$26.03Target Compensation Minimum:
$17.35Compensation will be commensurate to candidate experience.
Equal Employment Opportunity
The University of Louisville is an Equal Employment Opportunity employer. The University strives to provide equal employment opportunity on the basis of merit and without unlawful discrimination on the basis of race, sex, age, color, national origin, ethnicity, creed, religion, disability, genetic information, sexual orientation, gender, gender identity or expression, veteran status, marital status, or pregnancy. In accordance with the Rehabilitation Act of 1973 and the Vietnam Era Veteran Readjustment Act of 1974, the University prohibits job discrimination of individuals with disabilities, Vietnam era veterans, qualified special disabled veterans, recently separated veterans, and other protected veterans. The University acknowledges its obligations to ensure affirmative steps are taken to ensure equal employment opportunities for all employees and applicants for employment. It is the policy of the University that no employee or applicant for employment be subject to unlawful discrimination in terms of recruitment, hiring, promotion, contract, contract renewal, tenure, compensation, benefits, and/or working conditions. No employee or applicant for employment is required to endorse or condemn a specific ideology, political viewpoint, or social viewpoint to be eligible for hiring, contract renewal, tenure, or promotion.
Consistent with applicable law, demographic information is collected for aggregate reporting requirements. Demographic information provided through this application is not available to hiring managers/committees and is not considered in hiring or employment decisions.
Assistance and Accommodations
Computers are available for application submission at the Human Resources Department located at 2315 South First Street Walk, Room 02C - Louisville, Kentucky 40292.
If you require assistance or accommodation with our online application process, please contact us by email at employment@louisville.edu or by phone 502-852-6258.
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Find JobsEntry Level Clinical Research Associate Job Market
Who's Hiring
- Medpace33

- IQVIA14

- University of Miami13

- Johns Hopkins University12

- Medical College of Wisconsin9

Top Industries Hiring
- Education94
- Healthcare & Medical Services79
- Biotechnology & Pharmaceuticals42
- Consulting & Professional Services20
- Science & Research10
Entry Level Clinical Research Associate Jobs: Frequently Asked Questions
How do I get an entry level clinical research associate job?
Employers hiring at the entry level typically look for a life sciences degree, familiarity with Good Clinical Practice guidelines, and any hands-on experience coordinating or assisting in clinical trials. Internships, co-ops, or research assistant roles during school carry real weight. Highlighting your attention to detail, data integrity habits, and any exposure to regulatory documentation gives your application a concrete edge over candidates with a generic science background.
Which companies hire entry level clinical research associates?
Companies hiring entry level clinical research associates right now include Medpace, IQVIA, and University of Miami, based on current listings on Migrate Mate as of November 2026. Hiring at this level comes from a mix of contract research organizations, pharmaceutical companies, biotechs, and academic medical centers, all of which regularly bring on junior associates to support active trial portfolios.
Are there remote entry level clinical research associate jobs?
Yes, though many roles still require site visits or on-site presence. About 19% of entry level clinical research associate openings are remote or hybrid as of November 2026, reflecting the growth of decentralized trial monitoring and sponsor-based roles that handle oversight from a central office rather than traveling to sites full time.
Are these new grad clinical research associate jobs?
Yes, these listings include new grad, recent graduate, and junior clinical research associate roles. A posting is new-grad friendly when it explicitly welcomes zero to two years of experience, counts internships or research assistant work toward requirements, or accepts a strong academic background in place of full-time trial experience. New grad candidates who can show GCP training and organized documentation habits are competitive for these openings.
Which industries hire the most entry level clinical research associates?
Entry Level clinical research associate roles concentrate in Education, Healthcare & Medical Services, and Biotechnology & Pharmaceuticals, based on current listings on Migrate Mate as of November 2026. These sectors drive hiring at this level because they run continuous trial pipelines that depend on entry level associates to handle site coordination, data collection, and protocol compliance under the guidance of senior monitors.