Hybrid Part-Time Clinical Research Coordinator (Remote)

Actalent; Chattanooga (TN); Hybrid; USD 34,000 - 48,000; Part time

Benefits offered by this job

Medical, dental & vision

401(k) retirement plan

Life Insurance

Short and long-term disability

Health Spending Account (HSA)

Transportation benefits

Employee Assistance Program

Time Off/Leave (PTO)

Job summary

Actalent is seeking a Hybrid Part-Time Clinical Research Coordinator to support a clinical trial at a Chattanooga, TN site. The role involves identifying and enrolling participants, educating them about the study, and ensuring ongoing engagement and protocol adherence.

This is a 24-hour-per-week position with a flexible mix of remote and in-person work. The ideal candidate will have clinical research experience, knowledge of HIPAA and GCP, and strong organizational and communication skills to

Qualifications

• Experience as a Clinical Research Coordinator or similar role.
• 1+ year of experience in participant recruitment for clinical studies.
• Training in HIPAA regulations and patient privacy requirements.
• Training in Good Clinical Practice (GCP).
• Strong organizational and communication skills for fast-paced environments.

Responsibilities

• Identify, pre-screen, and recruit eligible participants for the clinical trial.
• Perform patient recruitment activities including phone screening and in-person discussions.
• Conduct community outreach to raise study awareness and generate referrals.
• Educate healthcare providers about study objectives, criteria, and procedures.
• Support participants to promote engagement and protocol compliance.
• Use EMR systems to review patient information and document recruitment activities.
• Follow GCP guidelines and protect participant safety and confidentiality.
• Maintain organized documentation of recruitment efforts and study records.

Skills

Clinical Research Coord

Patient recruitment

GCP training

HIPAA training

Job description

Actalent is seeking a Hybrid Part-Time Clinical Research Coordinator to support a clinical trial at a Chattanooga, TN site. The role involves identifying and enrolling participants, educating them about the study, and ensuring ongoing engagement and protocol adherence.

This is a 24-hour-per-week position with a flexible mix of remote and in-person work. The ideal candidate will have clinical research experience, knowledge of HIPAA and GCP, and strong organizational and communication skills to