Job Overview
As a Lead Research Clinical Coordinator, you will play a crucial role in conducting research activities within a clinical setting. You will be responsible for overseeing and participating in various research projects to advance medical knowledge and improve options available within our clinic for patient care. You will responsible for all aspects of study startups, site initiation, budgeting, IRB submissions, and most importantly, regulatory and compliance oversight.
Duties
- Work with sponsor for budgeting and finalizing site contracts
- Complete site initiation and start-up
- Supervise and coordinate clinical development activities
- Ensure compliance with Good Clinical Practice (GCP) guidelines and HIPAA regulations
- Submit FDA and IRB documents during study duration
- Create appropriate source documents
- Be famililar and able to upload data to EDC
-Effectively communicate study issues with the spondor , CRO and IRB as needed
- Utilize medical terminology effectively in research documentation
-- Conduct blood sampling and vital sign measurements
Skills
- Proficiency in data management and analysis
- Strong understanding of clinical research methodologies
- Knowledge of medical terminology and clinical trial processes
- Experience in supervising research activities
- Familiarity with clinical laboratory procedures
- Ability to adhere to HIPAA regulations in handling patient data
Job Type: Full-time
Pay: $50,000.00 - $109,235.00 per year
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Medical Specialty:
- Cardiology
- Gastroenterology
- Oncology
Schedule:
Ability to Relocate:
- Indianapolis, IN 46290: Relocate before starting work (Required)
Work Location: In person
