Physician (Research) - MD
Location
Bethesda, MD | United States
Job description
Role : Research Physician
Location : Bethesda, MD and Silver Spring, MD (must be able to report to both locations)
Hours : 40 Hours/Week
Pay : $145,000 - $185,000 /annually plus full benefits.
Type : Direct Hire
Clerance Requirement: Applicant must be able to obtain a T1/CAC Clearance.
Travel : Domestic and International Travel may be required
About : We are seeking a
Research Physician, Global Infectious Diseases to be based at our client site in Bethesda, Maryland, and Walter Reed Army Institute of Research (WRAIR) in Silver Spring, Maryland, supporting clinical research activities conducted by the WRAIR Military HIV Research Program (MHRP), the Emerging Infectious Disease Branch (EID), and other affiliated programs.
Under the supervision of the Director, Clinical Research Directorate, the Research Physician will contribute to a broad project portfolio in all stages of development, from concept to final report, inclusive of presentation at scientific conferences and publication in peer-reviewed literature. Projects that will be supported include Phase 1b clinical trials of broadly-neutralizing antibodies for the prevention and treatment of HIV; cohort studies evaluating the interplay of HIV, COVID-19, and neurobehavioral health; and other projects ranging from observational studies to clinical trials and vaccine product development. Activities will be executed both in the US and internationally.
We are seeking a qualified Research Physician (M.D. or equivalent) with experience in clinical medicine, excellent written/oral communication skills, experience or interest in regulated clinical research, and the ability to effectively lead and contribute to complex, multidisciplinary, international research.
Responsibilities - Contribute to the design and execution of clinical research studies to support the company and WRAIR missions, inlcuding observational and interventional studies related to the prevention and treatment of HIV and other infectious diseases.
- Participate in the submission and continuing review of clinical research protocols with all applicable Insitutional Review Boards (IRBs) and regulatory bodies, to include the U.S. Food and Drug Administration (FDA) and other relevant international and domestic agencies and collaborative partners.
- Conduct clinical research according to approved protocols as a study Principal Investigator, Protocol Chair, Associate Investigator, Consultant, or other designated role and maintain ethical and regulatory compliance as well as the integrity of study data and health and welfare of study participants.
- Conduct clinical research studies involving administration of investigational products according to the principles of current Good Clinical Practices (cGCP), Good Laboratory Practices (cGLP), and Good Manufacturing Practices (cGMP) and in accordance with all relevant host nation, US Federal, Department of Defense (DoD) and Army regulations and policies.
- Contribute to the creation, composition, maintenance and execution of clinical research protocols and supporting documents including study related budgets and status reports.
- Write and manage grant proposals to obtain funding from multiple funding sources.
- Coordinate scientific and laboratory input, output and analyses related to clinical research protocols and scientific goals, especially as it relates to vaccine research. Analyze data and prepare data and study findings for presentation at scientific meetings and publication in the peer-reviewed scientific literature.
- Generate relevant program status reports to the institution, government agencies, sponsors, research partners and others.
- Provide appropriate medical oversight and study-related clinical decision making including the identification, classification, management and reporting of adverse events.
- Examine, interview, counsel, and manage research participants in U.S. protocols, including protocols executed at Department of Defense facilities.
- Maintain licensure, credentialing, medical board certification and other certifications.
- Understand and implement the concepts and best practices of ethical research per CITI, HIPAA, and Good Clinical Practice training standards.
- Assist with management and coordination of research activities and communication between study sites and leadership at both project locations
- Coordinate with other members of project locations teams to train, support, and supervise additional research activities and personnel as needed.
- Perform other assignments as assigned and required in support of the companies missions.
Requirements: - MD, DO, or Equivalent Degree
- Licensure to practice medicine within the continental United States; Board certified or board eligible for certification in the specialty associated with the clinical research program.
- Minimum of 3-5 years experience required, inclusive of residency and/or fellowship
- Clinical Research Experience (training is okay)
- Excellent Written Communication skills, and preferably experience writing papers for scientific publication.
- Thorough knowledge of clinical medicine and demonstrated clinical competence.
- Excellent verbal, written, and interpersonal communication skills.
- Ability to successfully lead and/or participate as a member of complex, multidisciplinary research teams.
- Ability to make effective presentations and publish research data.
- Knowledge and experience with the development and execution of clinical research preferred but not required.
- Knowledge of U.S. regulations governing the conduct of medical research within the DoD and under the auspices of the FDA preferred but not required.
- Laboratory experience in the field of HIV immunology or related fields preferred byt not required.
- Some positions or sites may require that the incumbent be fully vaccinated against COVID-19. Proof of vaccination may be required.
Preferred Experience: - MPH or other advanced training in epidemiology, biostatistics, or related field
- Training/experience in HIV and/or infectious diseases (such as infectious disease fellowship training)
- Experience working in international settings
- Proven track record of scientific publications
Supervisory Responsibilities - May supervise multidisciplinary contract staff
Physical Capabilities - Position requires extended periods of standing and sitting
- Incumbent must be able to travel domestically and internationally and provide support to clinical research activities in potentially austere environments (up to 20% travel time expected).
Work Environment - This position will take place primarily in an office and laboratory setting.
Level One Personnel is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other status protected by law.
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