Physician

Description:

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, SARS, and nuerobehavioral 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 and contribute to complex, multidisciplinary, international research.

Contribute to the design and execution of clinical research studies to support the HJF and WRAIR missions, including 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 Institutional 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 HJF and WRAIR.

Coordinate with other members of the HJF and WRAIR teams to train, support, and supervise additional research activities and personnel as needed.

Perform other assignments as assigned and required in support of the HJF and WRAIR missions.

Additional Skills & Qualifications:

Can be someone who just came out of their fellowship or 1-2 years of experience. - Look for people still currently in fellowship getting ready to graduate out of infectious disease programs.

May supervise multidisciplinary contract staff.

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 but not required.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Salary : $125,000 - $185,000