Clinical Research Coordinator

Seacrest Behavioral Health; Atlanta (GA); On-site; USD 55,000 - 75,000; Full time

Job summary

Seacrest Behavioral Health in Atlanta is seeking a Clinical Research Coordinator to manage trial activities, recruit participants, obtain informed consent, schedule visits, and collect data.

You will ensure GCP and IRB compliance, maintain regulatory documents, and collaborate with investigators, clinicians, and patients to safeguard safety and data integrity, supporting smooth study operations. Strong teamwork and communication are essential.

Qualifications

• Attention to detail and organizational skills.
• Knowledge of clinical research protocols, regulatory requirements, and ethical standards.
• Ability to work collaboratively in a team environment.
• Excellent communication skills to interact effectively with stakeholders.

Responsibilities

• Coordinate clinical trial activities, including patient recruitment, informed consent, visit scheduling, and data collection.
• Ensure compliance with GCP, IRB, and sponsor regulations through accurate regulatory documentation.
• Collaborate with investigators, clinicians, and patients to promote safety, data integrity, and patient-centered care.
• Support study activities to facilitate smooth operations and accurate data management.

Skills

Attention to detail

Organizational skills

Clinical research knowledge

Regulatory & ethics knowledge

Team collaboration

Excellent communication

Job description

• Coordinate clinical trial activities, including patient recruitment, informed consent, visit scheduling, and data collection.
• Ensure compliance with GCP, IRB, and sponsor regulations through accurate regulatory documentation.
• Collaborate with investigators, clinicians, and patients to promote safety, data integrity, and patient-centered care.
• Support study activities to facilitate smooth operations and accurate data management.

Role:

• Coordinate clinical trial activities, including patient recruitment, informed consent, visit scheduling, and data collection.
• Ensure compliance with GCP, IRB, and sponsor regulations through accurate regulatory documentation.
• Collaborate with investigators, clinicians, and patients to promote safety, data integrity, and patient-centered care.
• Support study activities to facilitate smooth operations and accurate data management.

Responsibilities

• Coordinate clinical trial activities, including patient recruitment, informed consent, visit scheduling, and data collection.
• Ensure compliance with GCP, IRB, and sponsor regulations through accurate regulatory documentation.
• Collaborate with investigators, clinicians, and patients to promote safety, data integrity, and patient-centered care.
• Support study activities to facilitate smooth operations and accurate data management.

Qualifications & Skills

• Attention to detail and strong organizational skills.
• Knowledge of clinical research protocols, regulatory requirements, and ethical standards.
• Ability to work collaboratively in a team environment.
• Excellent communication skills to interact effectively with stakeholders.