Clinical research administrator vs research coordinator

Differences between clinical research administrator and research coordinator duties and responsibilities

Clinical research administrator example responsibilities.

• Manage regional academic and community base oncology practices as the primary contact for all communications and support.
• Ensure effective data management and the following of good clinical practice (GCP) guidelines.
• Initiate the development of standard operating procedures for regulatory compliance monitoring and auditing of regulatory and IRB documentation.
• Assist with reports and documents to FDA.
• Train new site personnel on specific clinical trial procedures and appropriate FDA regulations.
• Develop and implement program for continual review and quality assessment of regulatory and IRB documentation.
Show more

Research coordinator example responsibilities.

• Manage participant's records ensuring confidentiality as well as NIH specifications.
• Manage all IRB submissions, sponsor communications, participate in monitoring visits, drug reconciliation and dispensing.
• Recruit, screen, conduct psychometric examinations and collect data for pharmaceutical clinical trials in patients diagnose with Alzheimer's disease.
• Maintain confidential information and appropriate ethical professionalism with highly sensitive personal health information; take part in IRB human subjects training.
• Assist in preparation of grants, NIH progress reports, presentations, and manuscripts.
• Ensure and maintain confidentiality, privacy and compliance of patient rights in accordance with HIPAA regulations and NVCI policies.
Show more