Medical Director

Senior Medical OfficerJob Family: Clinical Trial Operations Travel Required: None Clearance Required: Ability to Obtain Public Trust What You Will Do: We are looking for a Senior Medical Officer to support NIAID/DMID by providing infectious disease expertise, protocol development support, pharmacovigilance review, and clinical safety consultation. This is a full-time position located in Rockville, MD.Responsibilities:Review pharmacovigilance reporting strategies, including safety monitoring plans and related safety documentation.Support protocol development activities by providing input on study objectives, subject safety, and safety reporting requirements.Provide clinical expertise regarding infectious diseases and make recommendations on key clinical issues.Serve as a clinical advisor to DMID staff and external stakeholders on study design and safety matters.Review incoming safety data, including adverse event reports, safety committee reports, clinical study reports, investigator brochures, package inserts, and scientific literature.Conduct comprehensive reviews of clinical protocols and supporting documentation.Provide recommendations to clinical investigators and program staff regarding protocol safety and implementation.Participate in discussions and presentations involving industry representatives, contractors, grantees, safety monitoring committees, and other stakeholders.Maintain proficiency in reviewing and accessing clinical study information from DMID-supported databases.Requirements:Medical degree from an accredited university.Minimum of SIX (6) years of medical, infectious disease, clinical research, or pharmacovigilance experience.Experience evaluating safety monitoring plans and adverse event reporting.Experience reviewing clinical research protocols and associated study documentation.Demonstrated knowledge of infectious disease clinical research.Proficiency with Microsoft Office applications.Must be able to obtain and maintain a Federal or DoD "public trust"; candidates must receive approved adjudication prior to onboarding with Guidehouse. Candidates with an active public trust or suitability are preferred.Nice To Have:Board certification in an infectious disease-related specialty.Experience supporting NIH-sponsored clinical trials.Experience presenting to regulatory, scientific, or executive audiences.Familiarity with safety monitoring committees and pharmacovigilance programs.Strong oral and written communication skills.Experience working with clinical research databases and electronic safety systems.The annual salary range for this position is $85,000.00-$141,000.00. Compensation decisions depend on a wide range of factors, including but not limited to skill sets, experience and training, security clearances, licensure and certifications, and other business and organizational needs. What We Offer: Guidehouse offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects our commitment to creating a diverse and supportive workplace. Benefits include:Medical, Rx, Dental & Vision InsurancePersonal and Family Sick Time & Company Paid HolidaysParental Leave401(k) Retirement PlanGroup Term Life and Travel AssistanceVoluntary Life and AD&D InsuranceHealth Savings Account, Health Care & Dependent Care Flexible Spending AccountsTransit and Parking Commuter BenefitsShort-Term & Long-Term DisabilityTuition Reimbursement, Personal Development, Certifications & Learning OpportunitiesEmployee Referral ProgramCorporate Sponsored Events & Community OutreachCare.com annual membershipEmployee Assistance ProgramSupplemental Benefits via Corestream (Critical Care, Hospital Indemnity, Accident Insurance, Legal Assistance and ID theft protection, etc.)Position may be eligible for a discretionary variable incentive bonus