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Senior Associate, Pharmacovigilance Coordinator

Cogent Biosciences Waltham, Vereinigte Staaten
On-site work

Publication date: 06/11/2026

The Pharmacovigilance Coordinator keeps the day-to-day engine of Pharmacovigilance (PV) Operations running. You will manage the PV inbox, track and distribute vendor safety deliverables, support commercial safety data reconciliations, and keep the PV deliverable calendar current. This is a hands-on role for an organized, detail-driven person who wants to build a career in PV within a growing team. Cogent Biosciences is a publicly traded biotechnology company focused on developing novel precision therapies to treat a broad range of patients with unmet medical needs.

Responsibilities

Monitor and triage the shared PV mailbox daily and route safety information, vendor correspondence, and partner requests to the correct owner within defined timelines; Log incoming items, track them to closure, and escalate time-sensitive safety information; File correspondence and supporting documentation in the PV repository to keep records inspection-ready; Track individual case safety reports through the vendor's case processing workflow, from receipt to submission; Escalate cases at risk of missing regulatory or internal timelines to the Senior Director, PVRM Operations; Assist in safety vendor oversight activities including tracking of KPIs, compliance metrics, and open query metrics; Maintain case tracking logs and support periodic case volume and timeliness reporting; Support periodic reconciliations of adverse events across commercial sources such as patient support programs, medical information, specialty pharmacy, and hub; Maintain reconciliation logs, sign-offs, and evidence for audits and inspections; Oversee receipt of scheduled line listings and other safety outputs from the PV vendor, confirming they arrive on time and are complete; Perform a first-pass quality check (correct period, format, and product) and follow up with the vendor on gaps or delays; Distribute line listings to the internal and external recipients defined in the distribution matrix and safety data exchange agreements, if relevant, and keep a record of each transmission; Maintain the distribution list and recipient matrix as stakeholders change; Own the PV deliverable calendar, including aggregate reports, line listings, reconciliations, and vendor deliverables, sending reminders ahead of due dates and flagging risks to on-time delivery; Schedule and coordinate PV meetings, including vendor governance, internal team, and cross-functional safety meetings, preparing agendas, taking minutes, and tracking action items; Support audit and inspection readiness by maintaining organized, complete PV records and trackers; Perform routine quality control of the PV CRO/Cogent SharePoint site; Help with SOP and work instruction updates, training records, and process improvement; Take on other PV Operations tasks as assigned

Requirements

At least 1 year in pharmacovigilance, drug safety, or a closely related function (medical information, clinical operations, quality); Working knowledge of adverse event reporting concepts and US FDA safety regulations; Familiarity with ICH and GVP guidelines; Strong organization and follow-through, able to manage many recurring deadlines at once; High attention to detail, especially when comparing data sets and documenting discrepancies; Clear written and verbal communication with internal teams and external vendors

Nice to have

Bachelor's degree in life sciences, pharmacy, nursing, health sciences, or a related field; Proficiency with Microsoft Outlook, Excel, Teams, and SharePoint; Experience with safety data reconciliation or safety data exchange with vendors or partners; Exposure to a safety database such as Argus Safety; Experience coordinating meetings, trackers, or calendars for a regulated function

Benefits

Competitive salary; Target bonus of 10%; Ongoing stock awards; 100% of medical, dental, and vision premiums covered for employee and family; Funding of up to 75% of in-network deductibles; 401(k) match with immediate vesting; Generous paid time off; 12 weeks of fully paid parental leave; Paid family and medical leave for all employees regardless of location; Company-paid short-term disability coverage for up to 20 weeks; Wellness programs; Tuition reimbursement; Inclusive family-forming support; Free on-site parking and gym facilities at the Waltham headquarters
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