We are seeking a Scientific Program Manager to support the National Institutes of Health's (NIH), world renowned National Institute of Allergy and Infectious Diseases (NIAID) in Bethesda, MD. Our NIAID professional, technical, and scientific support personnel are part of a preeminent team focused on positively impacting millions of lives around the world with groundbreaking research. Candidates will work at a prominent, diverse and vibrant NIAID worksite to directly support exciting ongoing research activities as a contractor team member. Accelerate your career and apply below to help us make a difference.
CAMRIS International is a dynamic clinical research and international development firm that achieves innovative solutions to health and development challenges through high-quality, cost-effective programs and research management services. We combine our proven systems with today's most effective, evidence-based best practices. Our core practice areas include: clinical research; vaccine research, microbiology and infectious disease research, development and production; biodefense; global health security; and HIV/AIDS programs.
Our employees enjoy a diverse, collegial environment where individual contributions matter at all levels. At CAMRIS, you will notably improve the lives of people at home and abroad.
Responsibilities
Coordinate activities with the Collaboration for AIDS Vaccine Discovery (CAVD) - Comprehensive Cellular - Vaccine Immune Monitoring Center (CCVIMC) with clinical sites and external stakeholders (CAVD Principal Investigators, BMGF, FNIH and IAVI).
Manage and report timelines for CCVIMC research activities and VRC translational activities with VRC leadership and external stakeholders.
Assist the Federal Task Leader in preparing budget proposals for CCVIMC B cell group and PREMISE.
Coordinate activities and input in regular meetings with VIP B cell analytics team.
Facilitate weekly, internal VIP- Translational Research Group team meetings.
Review VIP- Translational Research Group literature and distribute relevant manuscripts internally and externally.
Review and assist in gathering data and writing PREMISE and VIP-Translational Research Group manuscripts.
Liaise with partners for CCVIMC B cell group with other CAVD VIMC groups.
Assist the Federal Task Leader in administrative duties for VIP- Translational Research Group as needed, including updating the Annual Reviews on CCVIMC B cell group.
Participate in monthly progress update meetings with the Gates foundation, senior VRC leadership, FNIH and other external collaborators on CCVIMC B cell group activities.
Represent the CCVIMC B cell group in CAVD Project Team meetings.
Assist in preparation of clinical sections of regulatory documents for CAVD clinical studies.
Liaise with global partner clinical sites and VIP- Translational Research Group.
Prepare presentations for VIP translational research group.
Liaise with the CCVIMC Scientific Advisory Board at annual meetings.
Assist in preparing, answering, and clearing requests from external stakeholders.
Participate in publication of manuscripts with internal and external partners and stakeholders when appropriate.
Review B cell analysis data reports from external partners.
Coordinate activities with PREMISE and partner clinical sites, academic sites, industry partners, and VRC investigators/Program Heads.
Manage and report timelines for PREMISE research activities with VRC leadership and external stakeholders.
Coordinate activities and input in regular meetings with PREMISE team lead and directors.
Oversee non-human primate (NHP) trials for PREMISE, including design and execute PREMISE protocols for monoclonal antibody generation, and coordinate data analysis for these trials.
Assist with data analysis and presentation of findings.
Prepare presentations for PREMISE.
Qualifications
Ph.D. in Biology, Molecular Biology, or a related field is required.
10+ years of research experience, with 5+ years of experience in program coordination and evaluation is required.
Experience leading independent research projects related to infectious disease.
History of scientific publications and presentations.
Experience conducting scientific research and identifying program priorities.
CAMRIS International LLC offers competitive salaries and comprehensive benefits. Please submit your resume online at www.CAMRIS.com . CAMRIS is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran status, disability status, or any other characteristic protected by any applicable federal, state, or local law.
Some positions or sites may require that the incumbent be fully vaccinated against COVID-19. Proof of vaccination may be required.
Employment is contingent upon successful completion of a Public Trust-level background check, a requirement for this position under an active federal contract. The background check process may include, but is not limited to the following: (1) contacting your professional references; (2) verification of previous employment, education and credentials; (3) a criminal background check; (4) use/abuse of federally-controlled substances; and (5) a department of motor vehicle check. Candidates must be prepared to fully-complete any required background check questionnaire during initial onboarding.
