What are the responsibilities and job description for the Lead Clinical Research Coordinator position at SKY Clinical Research Network Group?
Company Description
SKY Clinical Research Network Group (SKYCRNG) is a consortium of private, practice-based research sites located strategically across Arkansas, Georgia, Illinois, Maryland, Mississippi, and Texas, within close proximity to hospitals. Renowned for its ability to deliver diverse participant populations and rapid enrollment, SKYCRNG supports high-quality Phase I-IV and outcomes-based clinical trials across therapeutic areas such as Cardiology, Neurology, Vaccines, Women's Health, and more. The network’s community-integrated model fosters trust-based recruitment, leveraging multigenerational patient relationships, pre-qualified participant pools, and ongoing community engagement events. SKYCRNG is staffed by Board-Certified providers and experienced research teams, offering comprehensive operational, regulatory, and centralized support for industry-sponsored clinical trials. With a commitment to quality and streamlined trial management, SKYCRNG exceeds enrollment diversity goals and accelerates startup timelines to provide impactful clinical data.
Role Description
This is a full-time, on-site role located in Union City, GA, for a Lead Clinical Research Coordinator. The individual in this role will oversee and coordinate clinical research studies, ensuring strict adherence to protocols and regulatory guidelines. Key responsibilities include obtaining informed consent, monitoring study participants, maintaining accurate study documentation, managing study-related communications, and collaborating with Principal Investigators and other research team members. The Lead Clinical Research Coordinator will play a critical role in driving excellent clinical trial execution while ensuring participant safety and data integrity.
Qualifications
SKY Clinical Research Network Group (SKYCRNG) is a consortium of private, practice-based research sites located strategically across Arkansas, Georgia, Illinois, Maryland, Mississippi, and Texas, within close proximity to hospitals. Renowned for its ability to deliver diverse participant populations and rapid enrollment, SKYCRNG supports high-quality Phase I-IV and outcomes-based clinical trials across therapeutic areas such as Cardiology, Neurology, Vaccines, Women's Health, and more. The network’s community-integrated model fosters trust-based recruitment, leveraging multigenerational patient relationships, pre-qualified participant pools, and ongoing community engagement events. SKYCRNG is staffed by Board-Certified providers and experienced research teams, offering comprehensive operational, regulatory, and centralized support for industry-sponsored clinical trials. With a commitment to quality and streamlined trial management, SKYCRNG exceeds enrollment diversity goals and accelerates startup timelines to provide impactful clinical data.
Role Description
This is a full-time, on-site role located in Union City, GA, for a Lead Clinical Research Coordinator. The individual in this role will oversee and coordinate clinical research studies, ensuring strict adherence to protocols and regulatory guidelines. Key responsibilities include obtaining informed consent, monitoring study participants, maintaining accurate study documentation, managing study-related communications, and collaborating with Principal Investigators and other research team members. The Lead Clinical Research Coordinator will play a critical role in driving excellent clinical trial execution while ensuring participant safety and data integrity.
Qualifications
- Expertise in obtaining Informed Consent and explaining study procedures to participants
- Strong understanding of Clinical Protocols and adherence to good clinical practices (GCP) standards
- Proven experience in Clinical Research and conducting Clinical Trials
- Ability to perform detailed Research and maintain high-quality study documentation
- Excellent organizational and communication skills
- Proficiency in using electronic medical records (EMR) systems and other research-related software
- A minimum of 2-3 years of clinical research experience preferred
- Bachelor’s degree in a healthcare, life sciences, or related field; certifications such as CCRC or CCRA are a plus