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$69

How much do clinical research representative jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for clinical research representative 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.

What are the key skills and qualifications needed to thrive as a Clinical Research Representative, and why are they important?

To thrive as a Clinical Research Representative, you need a solid background in life sciences or healthcare, knowledge of clinical trial protocols, and familiarity with regulatory guidelines such as GCP, often supported by a relevant degree. Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC), and certifications like CCRA or SOCRA are highly valued. Attention to detail, strong organizational skills, and effective communication are essential soft skills for success in coordinating studies and liaising with stakeholders. These competencies ensure that clinical research is conducted ethically, efficiently, and in compliance with regulatory standards.

What are Clinical Research Representatives?

Clinical Research Representatives are professionals who serve as liaisons between pharmaceutical or medical device companies and clinical research sites. They are responsible for ensuring clinical trials are conducted ethically, safely, and in compliance with regulatory standards. Their duties often include monitoring trial progress, educating site staff, collecting and verifying data, and ensuring proper documentation. Clinical Research Representatives play a key role in supporting the development of new treatments and therapies.

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

AspectClinical Research RepresentativeClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCRC are common
Work EnvironmentWorks primarily in clinical settings, hospitals, or research sites, assisting with patient interactions and data collectionManages the overall conduct of clinical trials, coordinating between sponsors, investigators, and patients
Employer & IndustryEmployers include pharmaceutical companies, research organizations, and hospitalsTypically employed by research sites, hospitals, or contract research organizations (CROs)

The Clinical Research Representative and Clinical Research Coordinator roles share similar educational backgrounds and work environments. However, the representative often focuses on patient interaction and data collection, while the coordinator oversees the entire trial process. Both roles are essential in clinical research but differ in scope and responsibilities.

How does a Clinical Research Representative typically collaborate with clinical trial sites and sponsors?

Clinical Research Representatives act as a vital link between clinical trial sites and sponsors, ensuring smooth communication and adherence to study protocols. They regularly visit sites to monitor progress, address issues, and provide training or support to site staff. Representatives also relay feedback to sponsors, help resolve operational challenges, and maintain documentation to ensure compliance with regulatory requirements. Strong interpersonal skills and effective project management are essential for fostering productive relationships and successful trial outcomes.
What cities are hiring for Clinical Research Representative jobs? Cities with the most Clinical Research Representative job openings:
What states have the most Clinical Research Representative jobs? States with the most job openings for Clinical Research Representative jobs include:
Clinical Research Representative jobs near you
Clinical Research Coordinator I

Clinical Research Coordinator I

DM Clinical Research

Philadelphia, PA

$24.50 - $32.50/hr

Full-time

Posted 9 days ago

Job description

Clinic Research Coordinator I
The Clinical Research Coordinator I, will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The CRC I will also ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.
Duties amp; Responsibilities:
  • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
  • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
    • a. Sponsor-provided and IRB-approved Protocol Training
    • b. All relevant Protocol Amendments Training
    • c. Any study-specific Manuals Training, as applicable
    • d. Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
  • Conducting study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
  • Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
  • Completing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
  • Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
  • Demonstrated understanding and implementation of Laboratory Manuals and protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration and laboratory kit inventory, under the direction of the Site/Study Management Team, for assigned protocols.
  • Liaising with Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives, under the direction of the Site/Study Management Team, for assigned protocols.
  • Submitting required administrative paperwork per company timelines.
  • Participating in subject recruitment and retention efforts.
  • Engaging with Research Participants and understanding their concerns.
  • Any other matters, as assigned by management.

Knowledge amp; Experience:
Education:
  • High School Diploma or equivalent required
  • Bachelor's degree a plus
  • Foreign Medical Graduates preferred
Experience:
  • At least one years of experience as a CRC, preferably with practice coordinating industry-sponsored vaccines in a private setting.
  • At least two years of experience as a research assistant, data coordinator, laboratory personnel, or equivalent experience in a clinical research setting
Credentials:
  • ACRP or equivalent certification is preferred
  • Registered Medical Assistant certification or equivalent is preferred
  • Knowledge and Skills:
  • Be an energetic, go-getter who is detail-oriented and can multi-task.
  • Be goals-driven while continuously maintaining quality.
  • Bilingual in Spanish is preferred

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