Job Information
Gilead Sciences, Inc. Senior Manager, France Affiliate Patient Safety H/F in Paris, France
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At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
Job Description
The Gilead Sciences, France Affiliate Patient Safety Senior Manager provides support to the Affiliate Head of Patient Safety (AHoPS) and global team to ensure strong engagement within the business ensuring engagement and integration within the affiliate. This position is involved in many aspects of pharmacovigilance coordination and execution at the affiliate and will provide back-up support to the AHoPS as required.
The France Affiliate Patient Safety Senior Manager performs the role of AHoPS back up/ local nominated Pharmacovigilance responsible person for France back up in accordance with local legislative requirements.
Key Responsibilities
Strategic PV partner
Patient Centricity: Responsible for bringing local insights to the decision-making process and into local benefit / risk and risk management development.
Local projects: Partner with Program Owners and commercial leaders to implement pro-active, efficient, and compliant solutions for the management of safety activities. Ensuring that relevant business partnerships have considered the impact to safety. e.g., awareness and input into new product launches and oversight of local solicited programs (Patient Support Programs, Market Research, Digital Media), providing support and review of contracts to ensure alignment with global standards. Partners to the global Patient Safety Solicited Program and Clinical Trial teams.
Local study strategic insights: Provide strategic input into local post marketing surveillance studies (PMS), local post approval safety studies, local sponsored studies, Investigator Sponsored Research (ISRs) and local early Access Programs called “Accès Précoce” and “Accès compassionnel”
Local Subject Matter Expert (SME) for product safety: Provide expertise on product safety knowledge and Patient Safety position on safety matters
Local Safety Contact Point
Point of contact within the Affiliate for safety related enquiries.
Audits and Inspections: Responsible for both internal PV audits and Regulatory Agency PV inspections in collaboration with Chief Pharmaceutical Officer (CPO) and local affiliates teams and global Patient Safety team.
Risk Management : Responsible for ensuring the appropriate development and revision of local RMPs and/or Country Specific Annexes in collaboration with global Patient Safety team and local Regulatory as required. Provide oversight & leadership of local risk minimization activities and materials as applicable.
Regulatory Intelligence & Industry Forums: Actively contribute to local industry forums, meetings, and seminars.
Maintain expert knowledge of local pharmacovigilance regulations.
Provide interpretation and communicate impact of changes in local pharmacovigilance regulatory requirements to global Patient Safety team
Feedback and influence local legislation consultations as appropriate
Communication of Safety Information: Provide leadership and local decision making in collaboration with global Patient Safety on communication of Safety Information to CPO and external & internal stakeholders, e.g.:
- Submit or delegates submission of relevant information to the authorities as required locally via collaboration with Regulatory and global Patient Safety. To include but not limited to; PSUR, signals, RMP, PMS & responses to Health Authority inquiries.
Communicate safety related issues and information that may be of relevance to the identification of potential safety signals to CPO, Patient Safety Therapeutic Area (TA) leads / qualified person responsible for pharmacovigilance in the European Union (EU QPPV) and local stakeholders.
Pro-active PV forecasting
Integration into Business: Act as the Patient Safety ambassador delivering proactive PV knowledge & support to the CPO and local Leadership Team
Leadership, forecasting, and strategy: Build and maintain effective business relationships across the affiliate to support the implementation of Patient Safety standards.
Local Programs and Research : Oversight of local studies and local commercial and medical affairs projects and perform pro-active plausibility assessments.
Safety Monitoring: Maintain overview of medicinal product safety profiles and any emerging safety concerns for company products locally.
Local Quality Management System
Ensuring that local pharmacovigilance activities are conducted such that the Affiliate(s) is in compliance with regulatory and internal company standards as set out within applicable regulations or guidance and global or local Procedural Documents (PDs).
Actively participate to the Quality Committee and annual quality review for Exploitant status
Responsible for local Patient Safety job descriptions, curriculum vitae, affiliate organisation charts and training records are up to date with local safety activities and personnel.
Maintain and input into local safety-related procedures.
Maintain and input into local vendor Audit requirement through the audit plan oversight, in collaboration with applicable local and global compliance teams.
Responsible for ensuring high visibility and communication of Patient Safety within the affiliate.
Training and engagement: Offer engaging internal and external training leveraging technologies and other innovative methods of engagement.
Training Affiliate(s) staff on safety reporting procedures including the timely reporting of safety information to Patient Safety / AHoPS as per French specific requirements e.g. French Charter.
Deviations / Non-Compliance: Investigate and provide input into any local non-compliance corrective action plans related to safety.
Responsible for review of the monthly global compliance reports produced by Patient Safety and taking necessary corrective actions locally as applicable.
Responsible for appropriate safety out of hours process in place and have appropriate oversight. Responsible for ensuring that the system is tested at least annually and that the test is documented.
Individual Case Safety Reports:
Perform annual review of Global Submission and Reporting Tool and provide real-time updates as applicable.
Ensure appropriate visibility of local safety data and where applicable provide local safety data to the global team.
If received, responsible for forwarding ICSRs to the global PS team for processing.
Ensuring that appropriate ICSRs are submitted to the local Regulatory Authority in a timely manner and in accordance with corporate and regulatory requirements where applicable
Responsible for performing applicable quality checks and off-label use assessment review of France cases recorded in the global safety database, review of Regulatory Authority submissions and review.
Management of local literature as applicable.
Business Continuity: In collaboration with global Patient Safety ensure local PV continuity plan in place and is exercised annually and maintained and communicated to global Patient Safety team.
Perform data checks as required to ensure no missed safety reporting within the affiliate for example non-AE checks.
Responsible for ensuring appropriate data retention timeframes in place in collaboration with global Patient Safety and in accordance with national requirements.
Ensure awareness of local data privacy requirements and acts locally/informs global Patient Safety as needed.
Local Legal Pharmacovigilance Role
Active participation in AHoPS network , meetings and sharing best practice
Perform the local QPPV role as applicable
Act as the safety consultant for CPO and local leadership teams
Local Pharmacovigilance System Master File: Responsible for timely update and oversight in collaboration with global Patient Safety as applicable
Maintain local knowledge in relation to Gilead Pharmacovigilance organization
Maintain expert local knowledge and oversight of:
the safety profile of locally marketed products and any emerging safety concerns or any non-compliant use identified according to the local requirement.
any information that may be of relevance to the identification of potential safety signals and communicating to global Patient Safety / EU QPPV and local senior management as applicable.
local studies and solicited programmes ongoing in the region and local post approval commitments
local licensing agreements (if applicable)
Responsible for oversight of local safety post approval commitments.
The Patient Safety resources such as the Agreement Repository, Patient Safety Shared drive and the Patient Safety webpage to ensure access to up to date information
KEY ROLE-RELATED COMPETENCIES / EDUCATION and/or EXPERIENCE REQUIRED
Pharmacist
Confirmed practical experience in pharmacovigilance
Ability to work with a high degree of autonomy
Comprehensive understanding of drug safety regulations and obligations
Proven leadership or influencing skills
Ability to represent Gilead externally
Excellent communication skills
Very good written and spoken English
Fluent French essential
For jobs in France:
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Equal Employment Opportunity (EEO)
It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual’s gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.
For Current Gilead Employees and Contractors:
Please log onto your Internal Career Site (https://www.myworkday.com/gilead/d/inst/13102!CK5mGhIKBggDEMenAhIICgYI1A0QtgI/cacheable-task/2997$2151.htmld#backheader=true) to apply for this job.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.