Medical Officer (52789) National Institutes of Health (NIH)

• Main Campus/Bethesda
• Bethesda, MD 20892 Apply Overview Salary Range $85.00
• $95.

00 Hourly Level Experienced Position Type Full Time Job Shift Day Education Level M.D.

Travel Percentage None Category Public Health Apply Description Position Objective:

The Medical Officer will provide support services to satisfy the overall operational objectives of the National Human Genome Research Institute (NHGRI) within the National Institutes of Health (NIH).

Duties and Responsibilities:

Coordinates all aspects of clinical protocol development, review and implementation. Provide advice on the oversight of clinical trials and protocols. Monitors ongoing clinical studies and clinical trials. Administer clinical and basic research projects, including clinical trials; monitor progress and conduct of projects, including protection and safety of participants in clinical trials. Perform periodic medical data review

• review laboratory values, adverse events, coding documentaries and data tables, listing and figures as needed.

Provide expertise for ongoing trials, including suitability of volunteers for enrollment into a study, consult for protocol PIs, and assist in safety oversight/assessments. Evaluates existing protocols and provides suggestions for design, execution and improvement. Collaborate with staff on the review, planning and implementation of clinical trials and ensure all concerns are addressed. Plan, implement, coordinate and evaluate programs and initiatives in the assigned specialty area of research. Establish goals and objectives for the assigned research area and organize efforts to initiate pioneering programs and resolve critical issues involving accomplishment of the research. Work with staff on protocol development; provide input on study safety design; identify medical and logistical problems that may impede the study; conduct reviews of clinical protocols and all supporting documents; and provide feedback to staff and clinical investigators. Assists in developing protocols for future clinical projects. Formulate concepts to foster research in new of underdeveloped areas of research. Produces various detailed reports for use by upper clinic or laboratory management. Help collect, collate, and analyze data pertinent to genetic disorders, and according to the research aims of the MGU. Review pertinent literature to provide a scientifically rigorous review of the subject matter. 4 Provide written scientific reports on specific symptom management topics as needed. 5 Participate in discussions of and prepare written summaries of evaluations of clinical trial concepts. Provide oral and/or written reports and status updates of on-going projects. Analyze data from clinical trials and research investigations; prepare abstracts for submission and manuscripts for publication. Update and maintain patient and protocol records; prepare reports are required. Evaluates various reports and safety monitoring plans and produces detailed reports for use by upper clinic or laboratory management. Participate in discussions of and prepare written summaries of evaluations of clinical trial concepts. Participates in site visits as needed. Take part in site visits to review and assess medical issues. Reviews the clinical protocols for safety of the study. Provide medical expertise in protocol follow-up stages for subject safety and protection. Provides advice and guidance for all clinical trials. Review clinical trial protocols. Reviews safety reports and provides recommendations for improvement. Provide medical expertise in protocol follow-up stages for subject safety and protection. Provides guidance to staff on various clinical processes and operational issues. Provide advice on the oversight of clinical trials. Develops policies and guidelines. Formulate concepts to foster research in new of underdeveloped areas of research. Coordinates and participates in various meetings, training and safety-related educational programs. Attend and participate in scientific meetings and conferences. 2 Collaborate on the planning, development, implementation and administration of research and training programs, projects, and contracts, conferences and workshops. 3 Work with Medical Genomics Unit (MGU) and collaborating/aligned research and related staff to perform services that help achieve the overall goals of developing and implementing new analytic approaches and technologies to better investigate a variety of genetic conditions. Assist with IRB-related research protocol requirements relevant to MGU studies. Assist with the management of research data and use and implementation of research databases in accordance with all applicable NIH/ NHGRI, and other policies. Participate in department standing meeting, training and safety related educational programs and efforts. 1 Meet with lab members to present updates Work products and documents related to contributing to ongoing research studies, including presentations (e.g., posters, lectures), manuscripts, and related materials. Work products and documents related to supporting administrative requirements for ongoing research, including submission of materials to the IRB and other regulatory and oversight entities. Work products and documents related to helping collect, collate, and analyze data pertinent to genetic disorders, and according to the research aims of the MGU Coordination of research subject activities. Work products and documents related to assisting with the formation and maintenance of collaborations with other investigators.

Qualifications Basic Qualifications:

Medical Degree in General Medical and Health Services from an accredited university Medical training Skilled in

Microsoft Office Preferred Qualifications:

Ability to communicate effectively, orally and in writing, with non-technical and technical staff Detail-oriented and possess strong organizational skills with the ability to prioritize multiple tasks and projects

• This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required by this position.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. GAP Solutions provides reasonable accommodations to qualified individuals with disabilities. If you need an accommodation to apply for a job, email us at recruiting@gapsi.com . You will need to reference the requisition number of the position in which you are interested. Your message will be routed to the appropriate recruiter who will assist you. Please note, this email address is only to be used for those individuals who need an accommodation to apply for a job. Emails for any other reason or those that do not include a requisition number will not be returned. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by law. This position is contingent upon contract award. Share job details to