Pharmacovigilance (PV)Case Management Head

Location: Bridgewater, NJ

Remote Work: Hybrid

Travel Expected: ~10% (domestic and international)

Job Type: Full time

About the Job

At Sanofi Consumer Healthcare, we have one shared mission – we work passionately, every day, to ‘serve healthier, fuller lives’ now and for the generations to come.

In order to do so, we strive to act as a force for good by integrating sustainability along our business and employees’ mission and operate responsibly from both a social and environmental point of view.

Everything we do is centered around people’s interests – our consumers, our customers, healthcare professionals, and our employees – across the world.

We are building loved brands that serve 1bn consumers worldwide, through our key platforms: Allergy, Physical & Mental Wellness, Pain, Digestive Wellness and Cough, Cold & Flu.

We aspire to become the best Fast Moving Consumer Health (FMCH) company In & For the world and we aim to build a work environment where people can thrive, grow, enjoy and be at their best.

Our Team

This is a Leadership member of the CHC PV Operations team and reports to the CHC PV Operations Head. This position includes responsibilities of Case Medical Safety lead.

This person is the process owner for case management globally in the Company, accountable for group wide alignment of ICSR management standards. Providing the strategic vision, planning and oversight on Inbound receipt, assessment & Health Authority submission of adverse events/ICSRs for all CHC PV customers globally and locally.

Main Responsibilities

Case Management Responsibilities:

  • To improve and reinforce globally integrated case management standards, procedures and systems in line with changes in the regulatory environment and best industry practices.

  • He/She is directly responsible to implement and manage the overall adverse event case processing including but not limited to case management for marketed CHC products, safety medical evaluation, HA reporting, Product Technical Complains (PTC) and management of medical device/drug device combination products.

  • Directly responsible for case management activities for USFDA, EMA & PMDA authorities.

  • Responsible to lead and support PV inspection/audit for US FDA, Japan PMDA and EMA

  • Manage oversight of PV case management activities through internal team leads and a service provider based in India.

  • To build synergy and partnerships with other global PV departments, PV teams within the affiliates/regions and science hub as well as with the external partners;

  • Ensure the vendors and distributors are qualified, high performing and motivated to accomplish the aligned objectives.

  • Ensure proper planning and execution of the changes approved by upper management with appropriate funding. This includes the management of external vendors and budget tracking for case management activities.

  • He/She contributes to safety management activities in cooperation with CHC Global Pharmacovigilance (GPV), Country PV teams, HA (Health Authorities), partner companies and other functions in compliance with global procedures and local regulatory PV requirements

  • To systematically evaluate the availability of resources for ICSR management and keep them trained according to global SOP, WIN and user manuals

  • To be aware of local/regional legal requirements for case management and data privacy that impact the task and generate globally valid operating standards

  • To drive business improvement for the tasks in collaboration with the involved CRO staff

  • To solicit local regulatory obligations from appropriate subject matter experts and assess impact to the global standardized process

  • To represent CHC global case management in all HA inspections and PV audits

  • Case Management expert leading all discussions involving internal/external stakeholder and Partner company about case management

Case Medical Safety Responsibilities:

  • He/She will be the Case Medical Safety Lead for CHC

  • Responsible for case (ICSR) medical safety activities in post marketing & clinical studies of CHC products

  • Lead the team of Case Medical Safety evaluators and oversee participation of case medical evaluators in safety analysis team for input of contextualized case data into the surveillance process and feedback on data requirements.

  • Early Identification and management of potentially important product safety issues of CHC products

  • Ensure essential PV foundational supported needed from case management to enable timely and proactive safety signal detection and risk management

  • Ensure availability of immediate safety alert reports, which enables Global Safety Officers to monitor the safety of our products and respond to inquiries from Health Authorities

  • Ensure High quality medical assessment of all adverse events

  • Responsible for appropriate training of all CMSE contributors

About You


  • PharmD or HCP equivalent with 10+ years of pharmacovigilance case management experience OR MD with 8+ years of experience in pharmacovigilance case management.

  • People management experience is preferred.


  • Knowledge of global and local PV regulations

  • Strong knowledge of the case management and medical safety evaluation in clinical trial and marketed products

  • Knowledge of PV safety system management. Experience with LSMV is preferred.

  • Appropriate experience of periodic reports, safety evaluation, risk management and communication with HA.

  • Knowledge of Project management or experience

  • Knowledge of PV Database and relevant PV tools used for PMDA


  • ICSR evaluation (seriousness, relatedness, unexpectedness and MedDRA coding) and HA reporting using PV safety system

  • Strong interest and ability to understand case relevant data, develop processes, including re-engineering of work flows and implementation of PV IT systems

  • Strong project leadership experience in a global environment; ideally including having led system or process implementation initiatives

  • Skill of fluent verbal and writing communication in English

  • Ability to manage and lead transversal meetings and small to moderate size groups and take appropriate decisions

  • Strong interpersonal skills and the ability to collaborate productively in an international and multi-cultural environment

  • Proficiency in Microsoft applications (Word, Power Point, Excel)

Pursue Progress, Discover Extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at ( !