Remote-Ready Clinical Research Coordinator — Part-Time (Chattanooga)

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

Benefits offered by this job

Medical, dental & vision

401(k) plan

Life Insurance

Disability insurance

Health Spending Account

Transportation benefits

Employee Assistance Program

Time Off / 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 includes recruiting eligible participants, educating them about the study, and ensuring engagement and protocol adherence with research staff.

The position requires clinical research experience, strong organizational skills, and confident communication with participants and providers.

Qualifications

• Proven experience as a Clinical Research Coordinator or clinical research experience.
• At least 1+ year of experience in patient recruitment for clinical research or clinical trials.
• Familiarity with clinical trial processes and protocols.
• Training in HIPAA regulations and patient privacy requirements.
• Training in Good Clinical Practice (GCP).
• Strong organizational skills with the ability to manage multiple tasks and deadlines.
• Confident verbal and written communication with participants, providers, and research staff.
• Ability to work effectively in a fast-paced environment with high accuracy.

Responsibilities

• Identify, pre-screen, and recruit eligible participants for the clinical trial through community outreach and other recruitment strategies.
• Perform patient recruitment activities, including phone screening, in-person discussions, and follow-up communication to support enrollment goals.
• Conduct community outreach efforts to spread awareness of the study, including visiting local community locations and attending community events.
• Partner with local clinics, medical practices, and medical professionals to generate patient referrals for the clinical trial.
• Educate healthcare providers about the clinical trial, including study objectives, eligibility criteria, and participant qualifications.
• Explain study procedures, expectations, and requirements to potential participants in a clear and empathetic manner.
• Support participants throughout the trial to promote engagement, adherence, and protocol compliance.
• Collaborate closely with research staff and investigators to ensure accurate and timely execution of study-related activities.
• Use electronic medical records (EMR) systems to review patient information, support pre-screening, and document recruitment activities.
• Follow Good Clinical Practice (GCP) guidelines and privacy regulations to protect participant safety and confidentiality.
• Maintain organized documentation of recruitment efforts, participant interactions, and study-related records.
• Contribute to a fast-paced research environment by managing multiple tasks and priorities with strong attention to detail.

Skills

Clinical Research Coordinator

Patient recruitment

HIPAA training

GCP training

Organizational skills

Verbal communication

Written communication

Fast-paced environment

Job description

Actalent is seeking a Hybrid Part-Time Clinical Research Coordinator to support a clinical trial at a Chattanooga, TN site. The role includes recruiting eligible participants, educating them about the study, and ensuring engagement and protocol adherence with research staff.

The position requires clinical research experience, strong organizational skills, and confident communication with participants and providers.