Highly qualified medical research professional skilled in all aspects of clinical trial coordination, protocols, and participant relationships. Experienced in both medical practice and clinical research environments. Demonstrate strong working knowledge of ICH-GCP, company standard operating procedures, regulatory guidelines, protocols and monitoring guidelines. Communicate effectively with medical personnel, colleagues, and study participants. Consistently perform at peak professionalism, adhering to code of ethics and business standards. Experienced in multiple study areas, device studies, verifications all information pertaining to shipment receipt ,use and return of device, as we as cardiovascular, studies ensure compliance with internal policies and procedure. Submit document to the institutional Review board to follow process and ensure approval. time and task management, sound problem solving skills and flexibility.
Complete Written and Verbal English
MS Office Products (word, excel, power point)
Fast Learner
Adaptable
Flexible
Extreme Attention to Detail
Ability to Travel without Limitations
Strong Knowledge of Medical Terminology
Electronic Medical Records
Documentation& Reporting
Strong Work Ethic
Time Management
ICH Good Clinical Practice (GCP) | Cardiopulmonary Resuscitation (CPR) Health Insurance Portability and Accountability Act (HIPAA) | Blood Borne Pathogens Certification. Phlebotomy training. MoCA Certification( Cognitive Assessment) Medidata Rave EDC, CITI Programme with investigational Drugs and medical Devices Training.CITO Programme with Conflict of interest , Biosafety /Biosecurity Training., Shipping and Transport of Regulated Materials Trainning