I am an RN, certified in clinical research through ACRP. I have 15 years of management experience at a major cancer center and 5 years of clinical monitoring experience both in the field and in-house. For the purpose of clarification, I also have 5 years of clinical research experience as a study coordinator in medicine outside the field of oncology
I would like to find a position that matches my level of experience in the...
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ICH-GCP, Clinical Research Associate, ACRP Certified, Regulatory, Medical Oncology, Medical Device
Achieve the successful of clinical trial and ensure the subject safety and the high data quality by working closely with each clinical site and ensure that all the tasks are being conducted in accordance with the clinical trial protocol , ICH GCP guidelines and local regulations.
Dear Hiring Manager,
I am interested in exploring career opportunities with your company and have therefore enclosed my resume for your review. This position seems ideal for my experience, education, skills, and career interests. I am eager to contribute my enthusiasm and teamwork to your organization.
My professional goal is to enhance my research development and senior leadership experience. I believe that I could...
High energy professional with exceptional interpersonal, communication and leadership skills. Resourceful, creative and loyal.
Ideal Companies: Hospitals, CRO
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Oracle Management System, Citrix, Case Reimbursement, Website Maintenance, Access
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Clinical Operations, Vendor, GCP, Budgets, Study Management, Drug Development
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GCP Auditor, Clinical Auditor, GLP Auditor, Quality Assurance, Clinical Trails, Good clinical practice
Seeking a position with a start up or established company where I can apply my diverse management and quality compliance experiences and skills to further my professional and personal growth.
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Medical Devices , Project Management, Veterinary Technology , Communication , Biomedical Leadership & Training , Preclinical & Clinical Trials , Safety Protocols , Regulatory Compliance Process Improvement , Facility Management , Research, Quality Assurance , Regenerative Medicine, Product Development , Supply Chain Management , Vendor Relations, Strategic & Tactical Planning , ISO 13485, GMP/GLP/GCP, Administrative
Monitor assigned clinical trials, interact with all different department such as (monitoring resources, project manager, quality assurance and data management). Conduct site visits (initiation, monitoring and close out). Ensure the adherence to FDA, ICH & GCP regulations. Instruct the site staff in their roles and responsibilities in conducting clinical trials. Ensure the completion and collection of regulatory document...
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Clinical Research Coordinator, Data Manager, Medical Assistant
