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Clinical Research Study Physician

Company: Healthcare in Central Florida
Location: Orlando
Posted on: March 14, 2018

Job Description:

Job DescriptionSummary of Position:Performs various medical tasks, assessments, and activities related to the successful running of a clinical trial while providing exemplary customer service in order to ensure effective and efficient operations.Key Responsibilities: Serve as Principal Investigator and/or Sub-Investigator for a number of clinical trials; Performing tasks such as physical and medical history assessment, rating scales, and the overall medical management of subjects on a trial. Additionally, the study physician may participate at Pre-study visits, Site Initiation visits and other customer facing meetings. Ensure and protect the patient’s welfare and rights as a research subject; Be thoroughly familiar with the protocol, case report form, informed consent, source documentation, patient diary (when applicable), and study medication(s) for the assigned research study; Adhere to all company SOPs and covenants, GCP, ICH, HIPAA, NIH, FDA Regulations and SOPs and maintain ongoing regulatory documents; Establish rapport with sponsor representatives and maintain frequent face-to-face, written and telephone contact with various persons involved in the study, including but not limited to the patients, doctors, pharmaceutical sponsors and all levels of the company; Assist and participate in study recruitment to ensure enrollment goals are met or exceeded; Direct and guide Research Staff on study specific medical tasks; Utilizes and ensures the appropriate equipment is on-site for Universal Precautions for themselves and others in and around areas that may contain potential biohazards; Perform appropriate research protocol procedures which may include, but are not limited to: physical exams, medical history review and assessment, assessment of; vital signs, laboratory results and adverse events; Work with Site Director, Sub Investigator(s), and Study Coordinator(s) to maintain high quality and patient safety; May dispense investigational product and instruct subjects on usage and potential drug interactions; Practical knowledge of document processes and reporting of SAEs, 1572s, CRFs, ICFs, etc.; Participate in training for other study physicians, nurses and staff on research protocol; Provide patient education regarding disease process and involve patient in decision-making processes; Maintain accountability of own ongoing professional growth and development; Perform necessary functions as approved by the organization, for the conduct of clinical research; Travel including between company offices and to study investigator meetings; May perform other duties not specifically listed in this job description. Qualifications:A Medical degree (MD or DO) and current license (in good standing) to practice as a physician in the state of Florida and prescriptive authority is required. Unrestricted ability to participate in federal programs. Previous clinical research experience is preferred; High degree of clinical experience, skill and assessment to ensure subject safety; Excellent verbal and written communication skills; Well-developed interpersonal skills and the ability to work well independently as well as with co-workers, peers, supervisors and external customers; Must be professional and have a strong work ethic; Must possess a high degree of integrity and ability to maintain confidentiality with HIPAA guidelines, patient matters and other sensitive information.

Keywords: Healthcare in Central Florida, Orlando, Clinical Research Study Physician, Healthcare, Orlando, Florida

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