Pharmacovigilance Physician

Tunnell Government Services, Inc.; Bethesda (MD); Hybrid; USD 120,000 - 180,000; Full time

Job summary

Tunnell Government Services, Inc. is seeking a Pharmacovigilance Physician (FTE) to provide continuous pharmacovigilance support, ensure regulatory reporting compliance, and develop safety and surveillance plans for assigned programs.

The role requires a US license and offers hybrid work in Frederick, MD with two days on-site. The position involves managing adverse event data, coordinating DSMB/Committee activities, and preparing safety documentation for regulatory authorities, with a focus on

Qualifications

• Provide continuous pharmacovigilance support in accordance with regulatory timelines and sponsor SOPs.
• Develop safety plans and surveillance plans for products/protocols.
• Establish DSMB/Committee structures and meeting processes.
• Process safety events using electronic systems and generate safety narratives.

Responsibilities

• Receive, evaluate, and manage adverse event reports, ensuring 24/7 coverage.
• Coordinate DSMB/Committee meetings and document outcomes.
• Review clinical protocols and相關 documents for pharmacovigilance relevance.
• Prepare regulatory submissions and safety communications as required.

Skills

Pharmacovigilance

Regulatory reporting

Safety surveillance

Data review

Clinical trials oversight

FDA/ICH knowledge

Tools

Argus

Job description

Tunnell Government Services, Inc., is comprised of the industry’s leading scientists, medical and technical experts, and human capital and organizational development professionals. We approach all projects as a team and are committed to helping our clients transform and quickly achieve strategic goals. If you are interested in joining an employee-owned company that develops and implements innovative, integrated and differentiated solutions, please click on the links below to find the job that is right for you and contact us.

Title: Pharmacovigilance Physician (FTE)

Location: Fredrick, MD (Hybrid- two days a week on-site)

Requirement: US License

• Provide continuous pharmacovigilance support to receive, assess, and elevate adverse event reports IAW regulatory timelines and sponsor SOPs including intake, triage, assessment, and reporting of adverse events, ensuring 24 hours per day, 7 days per week coverage, including holidays and weekends.
• Develop pre-market and post market safety plans.
• Surveillance plan(s) specific to products/protocols that include signal detection tools and templates necessary to implement the safety surveillance
• Develop and maintain safety management plan(s) that delineate the roles, responsibilities, processes, and timelines for safety activities and drives the execution of the safety related activities during a trial
• Establish Data Safety Monitoring Boards (DSMB)/Committees, which includes identifying members, developing, reviewing and finalizing the initial Charter and any revisions
• Schedule and coordinate DSMB/Committee Meetings (organizational, in-process, executive, and ad hoc), including a face-to-face initial DSMB/committee organizational meeting at a central location within the continental United States, and provide an agenda.
• Develop and prepare written DSMB meeting minutes for each meeting per SOPs
• Provide the DSMB/Committee Chair Recommendation(s) form, completed and signed by the DSMB/Committee Chair within 24 hours of the meeting conclusion, documenting the DSMB/Committee decisions and recommendations to the Safety Office
• Provide pharmacovigilance support that includes but is not limited to reviewing clinical protocols and associated documents, conducting literature searches, providing risk-benefit analyses, developing comprehensive risk mitigation plans, and writing white papers
• Provide pharmacovigilance guidance and subject matter expertise
• Receive, process, evaluate, and manage reported safety cases through electronic systems, such as Argus, which may include but are not limited to data entry and preparation of serious adverse event narratives, generating analyses of similar events, data element coding of event terms in the safety database utilizing the Medical Dictionary for Regulatory Activities and preforming quality control reviews of the entered data
• Monitor the safety mailbox at a minimum twice a day 7 days a week, to include weekends and holidays, for new incoming unexpected and related serious adverse events
• Triage safety reports, interpret clinical data, and perform regulatory evaluation for regulatory reporting purposes
• Track follow-up information /correspondence through to case closure
• Report serious adverse events to the FDA and other applicable regulatory authorities IAW 21 CFR 312.32 and 312.33, and ICH Guidelines
• Identify database cases eligible for archiving and assist with archiving all documents in compliance with government internal standards and regulatory guidelines
• Provide strategic input or oversight for regulatory documents including, but not limited to, Investigational New Drug application safety reports (MedWatch), annual reports, and final clinical study reports
• Notify the investigator(s) of safety information, including expedited serious adverse events, according to Government procedures and IAW 21 CFR 312.32 and 312.33 and ICH Guidelines
• Manage and process reported pregnancy cases through electronic systems, which may include but is not limited to data entry and preparation of narratives, generating and sending follow-up queries as appropriate until term, generating analyses of similar events, data element coding of event terms in the safety database utilizing the Medical Dictionary for Regulatory Activities dictionary and performing quality reviews of data entered into the electronic data management system and other systems as applicable
• Reconcile data and documentation in the Safety Database and the Clinical Database at a minimum annually before the annual report and before study database lock
• Develop and/or review protocol specific documents and clinical safety documents including but not limited to clinical protocols, informed consent forms, investigator brochures, data monitoring committee charters, safety management plans, safety surveillance plans, safety-related source document and other associated clinical safety documents
• Develop a protocol/product specific unblinding plan prior to the start of a clinical trial
• Work with clinical monitors and site staff to resolve issues and obtain needed documentation.

Must be a US Citizen or a full Green Card holder.

Tunnell strives to hire and retain the most qualified talent. We believe that having employees with different backgrounds and capabilities contributes to the success of our business. To attract qualified applicants, Tunnell posts to a wide variety of job sites. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Please be advised that certain client contracts may outline specific requirements for onsite work. Tunnell employees and/or contractors are expected to comply with all client requirements, including any safety and health protocols.