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Clinical Research Site Manager

Company: Medical Science & Computing
Location: Bethesda
Posted on: October 18, 2020

Job Description:

Careers --- MSC --- Clinical Research Site Manager in Bethesda, Maryland - Careers at Bethesda Skip Branding Home What We Do Contract Vehicles Careers Contact Us Careers Privacy Policy Terms o f Use Careers --- MSC --- Clinical Research Site Manager in Bethesda, Maryland - Careers at Bethesda Skip to Main Content Please Enable Cookies to Continue Please enable cookies in your browser to experience all the personalized features of this site, including the ability to apply for a job. Welcome page Welcome page Returning Candidate? Log back in Clinical Research Site Manager Job ID 2020-4235 of Openings 2 Job Location(s) US-MD-Bethesda Posted Date 2 days ago (10/5/2020 5:47 PM) Category Science Overview Medical Science & Computing (MSC), a Dovel company, is an exciting growth oriented company, dedicated to providing mission critical scientific and technical services to the Federal Government. We have a distinguished history of supporting the National Institutes of Health (NIH) and other government agencies. MSC offers a dynamic and upbeat work environment, excellent benefits and career growth opportunities. We attract the best people in the business with our competitive benefits package that includes medical, dental and vision coverage, 401k plan with employer contribution, paid holidays, vacation, Medical and Flexible Spending Accounts, Pre-Tax Transit Assistance and tuition reimbursement. If you enjoy being a part of a high performing, professional service and technology focused organization, please apply today Duties & Responsibilities MSC is searching for a Clinical Research Site Manager to provide support to the National Institutes of Health (NIH). This opportunity is a full-time position with MSC and it is on-site in Bethesda, Maryland. Implement and coordinate a range of individual clinical site-management activities Advise PIs on clinical site start-up and relevant operational and regulatory issues including resource allocation, personnel management, and administrative issues Provide leadership for planning, organizing, and conducting site visits or reverse site visits to clinical trials units to effectively fulfill site management responsibilities. Assess the level of clinical trials research competency of clinical research sites and the extent of research knowledge and technology available to achieve the desired quantity and quality of the clinical trials units. Direct and conduct formal evaluations of the clinical trials units--- organizational structures and modes of operations in relationship to the achievement of the Division---s goals and objectives in the areas of administration, clinical site management, and recruitment of patients. Provide oversight and technical direction for evaluation of site performance using data compiled by the network data management centers. Identify problems or issues that transcend individual units or trends that indicate the need for procedural clarification or policy development and recommends follow-up actions or policy directives to Branch Director or Branch Chief Conduct trainings at sites and Network meetings on relevant policies/regulations Attend Network meetings, conference calls, ad hoc meetings and working groups. Support federal Program Officers by: 1) tracking and summarizing grantee compliance with training requirements, grantee progress in meeting the grant aims by reviewing progress reports, and adherence to applicable regulations; and 2) reviewing training manuals, policies and procedures Participate in the creation and review of study or site closure-related documents and checklists Interface with networks, investigators, Operations Centers, to share information and collaborate on research and site-related issues Prepare oral and written presentations for internal and external programmatic and scientific meetings. Requirements Master---s degree in Health Science, Public Health or a related field. A Bachelor---s degree or R.N. with two (2) years of related experience can be considered equivalent. Minimum of three (3) years of experience in clinical research with an emphasis on regulatory experience. In-depth knowledge of clinical research operations, regulatory affairs, GCP, and other related clinical research issues. Experience planning, organizing and conducting clinical site visits. Experience advising on site evaluations and provide recommendations on courses of action. Excellent verbal and written communication skills. Medical Science & Computing (MSC), a Dovel company, is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status. Options Apply for this job online Apply Share Email this job to a friend Refer Sorry the Share function is not working properly at this moment. Please refresh the page and try again later. Share on your newsfeed Loading Application FAQs Software Powered by iCIMS www.icims.com

Keywords: Medical Science & Computing, Bethesda , Clinical Research Site Manager, Professions , Bethesda, Maryland

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