Skilled in all aspects of clinical trial coordination,protocols and participant relationships especially in Cardiovascular pulmonary studies. 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. Effective Communication with medical personnel, colleagues, and study participants. Consistently perform at peak of professionalism by adhering to code of ethics and business standards. Experienced in multiple study areas, such as Device studies, Drug Studies .Verifications of all information pertaining to shipment receipt ,use and return of device. 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. Detail-oriented Research Analyst with first-rate active listening. Creative and persistent to quickly and effectively solve various problems that may arise within
the department. Committed to completing accurate and thorough competitive assessments.
Hardworking and passionate job seeker with strong organizational skills eager to secure position. Ready to help team achieve company goals. Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities.
Extreme Attention to Detail
Ability to travel without Limitations
Strong Knowledge of Medical Terminology
Electronic Medical Record
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 Training. BSC Rave 5.6 EDC Data Entry Training for Clinical research Cordinator.CITI programme course for conflict of interest under requirement by Baylor scott& White Research institute.
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 Training. BSC Rave 5.6 EDC Data Entry Training for Clinical research Cordinator.CITI programme course for conflict of interest under requirement by Baylor scott& White Research institute.