Clinical Research Coordinator: Enrollment & Study Operations

Actalent; Utah; On-site; USD 34,000 - 48,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Disability insurance

HSA

Transportation benefits

Employee Assistance Program

Paid time off

Job summary

Actalent in Salt Lake City, UT is seeking a Clinical Research Coordinator to support a Pneumococcal Disease trial. You will drive enrollment, engage with participants, and collaborate with research staff to ensure quality data and protocol adherence.

The role requires strong clinical research experience, superb organization, and ability to work with patients and multidisciplinary teams in a fast-paced environment. This is a full-time onsite contract through December 2026 with potential extension.

Qualifications

• Proven experience as a Clinical Research Coordinator.
• At least 2 years of patient recruitment experience.
• At least 2 years using EMR in clinical/research settings.
• HIPAA regulations training completed.
• GCP training completed.
• Strong organizational skills and attention to detail.
• Clear communication with participants and staff.

Responsibilities

• Review charts using EMR to assess eligibility against criteria.
• Pre-screen potential participants for suitability.
• Educate participants about study purpose, procedures, risks and requirements.
• Follow up with participants to support retention and protocol adherence.
• Schedule in-person visits and ensure alignment with timelines.
• Send reminders and visit information to participants.
• Support recruitment strategies and document activities.
• Maintain accurate documentation in EMR and study systems.

Skills

CRC experience

Recruitment

EMR usage

HIPAA training

GCP training

Organization

Communication

Tools

EMR software

Job description

Actalent in Salt Lake City, UT is seeking a Clinical Research Coordinator to support a Pneumococcal Disease trial. You will drive enrollment, engage with participants, and collaborate with research staff to ensure quality data and protocol adherence.

The role requires strong clinical research experience, superb organization, and ability to work with patients and multidisciplinary teams in a fast-paced environment. This is a full-time onsite contract through December 2026 with potential extension.