Hybrid Clinical Research Coordinator — Part-Time, Remote

Actalent; Oklahoma City (OK); Hybrid; USD 34,000 - 48,000; Part time

Job summary

Actalent in Oklahoma City, OK is seeking a Hybrid Clinical Research Coordinator for a part-time, 20-hour-per-week role supporting a clinical trial at a local site. You will focus on identifying and recruiting eligible participants, educating them about the study, and ensuring ongoing engagement and compliance.

The position offers flexible scheduling, with most hours remote. Candidates should have clinical research experience, strong organizational skills, HIPAA and GCP training, and the ability

Qualifications

• Proven experience as a Clinical Research Coordinator.
• At least 2 years of patient recruitment experience.
• Hands-on pre-screening experience.
• Training in HIPAA and privacy requirements.
• Training in Good Clinical Practice (GCP).
• Excellent organizational skills with strong attention to detail.
• Confident communication with participants and staff.
• Ability to work independently with clinical and research teams.

Responsibilities

• Perform patient recruitment activities through community outreach to raise trial awareness.
• Partner with local clinics and medical professionals to generate referrals.
• Educate healthcare providers about the trial's objectives, procedures, and eligibility criteria.
• Pre-screen patients to determine eligibility based on study requirements.
• Visit community locations and events to promote the study and engage potential participants.
• Explain procedures and expectations to support informed decision-making.
• Maintain accurate documentation of recruitment and screening activities.
• Collaborate with research staff to coordinate enrollment and follow-up.
• Adhere to GCP guidelines and HIPAA regulations in all interactions.

Skills

Clinical Research Coordinator

Patient recruitment

HIPAA training

GCP training

Organizational skills

Verbal and written communication

Independent work

Job description

Actalent in Oklahoma City, OK is seeking a Hybrid Clinical Research Coordinator for a part-time, 20-hour-per-week role supporting a clinical trial at a local site. You will focus on identifying and recruiting eligible participants, educating them about the study, and ensuring ongoing engagement and compliance.

The position offers flexible scheduling, with most hours remote. Candidates should have clinical research experience, strong organizational skills, HIPAA and GCP training, and the ability