Job Title: Associate Director Drug Safety and Pharmacovigilance Operations
Job Location: Cambridge MA USA
Job Location Type: Remote
Job Contract Type: Fulltime
Job Seniority Level: MidSenior level
The Company
With deep expertise in chemistry Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting earlystage company bringing together experienced scientists and industry veterans with a proven track record in drug discovery oncology drug development and company building.
The Role
Reporting to the Senior Director of Pharmacovigilance (PV) Operations the Associate Director of PV Operations will be responsible for PV’s role in expanded & early access programs (EAP) across the portfolio and other PVrelated projects as assigned (e.g. Crossreporting of SUSAR; Support Call Center for PVrelated questions). The role will expand and evolve in line with Nuvalent’s expansion as we approach potential market authorization.
Responsibilities
Oversight of EAP vendor including but not limited to safety data exchange agreement maintenance and compliance monitoring
Adverse event reconciliation between databases
Oversight of safety reporting requirements for all EAP countries
Primary point of contact for PV requests within the EAPs
Support PV Operations team activities to ensure cross coverage across the portfolio
Support regulatory inspections and serve as subject matter expert on PV’s role in EAPs
Identify potential risks and opportunities within the EAPs keeping PV Leadership informed for proactive decisionmaking
Competencies Include
Excellent oral and written communication skills with high emotional intelligence
Track record of effective decisionmaking and conflict management/resolution skills
Ability to work in a collaborative environment and build effective working relationships across the organization and with external stakeholders/vendors
Detail and process orientated with excellent project management problem solving and organization skills.
Ability to think critically with strong attention to detail effectively communicating verbally and in writing.
Demonstrated project management and prioritization capabilities
Qualifications
Bachelor’s degree in a relevant field or related experience.
8 years of relevant experience within the biotechnology or pharmaceutical industry including 4 years of experience in Pharmacovigilance operations
Handson expert knowledge of Argus or equivalent PV database.
Ability to interpret and follow regulatory guidelines.
Proven knowledge of Good Documentation Practices and cGXPs.
Basic knowledge of MedDRA coding.
Experience in ICSR caseprocessing and reporting.
Strong knowledge of current and emerging regulatory requirements including EMA GVP Modules FDA IND and NDA reporting requirements ICH CIOMS
Expert knowledge of pharmacovigilance activities and processes preferably in multiple PV functional areas
Direct experience managing relationships with service providers or external business partners
Nuvalent provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion race creed color sex sexual orientation alienage or citizenship status national origin age marital status pregnancy disability veteran or military status predisposing genetic characteristics or any other characteristic protected by applicable federal state or local law.
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