2 Pharmacovigilance Scientist jobs in the United Arab Emirates
Regional Pharmacovigilance Operations Manager
Posted today
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Job Description
This role is accountable for overseeing day-to-day operations and compliance activities to maintain high-performing pharmacovigilance systems across assigned regions. The successful candidate will be a key partner for affiliate safety representatives and medical directors in driving excellence in pharmacovigilance across affiliates.
Responsibilities:
- Oversee resources executing compliance and operational activities in affiliates within assigned regions, ensuring high-performing pharmacovigilance systems.
- Proactively anticipate and address operational issues and opportunities within regions through deep understanding of regulatory environments, operational metrics, and business priorities.
- Ensure timely communication of operational issues and compliance risks to area pharmacovigilance heads and key stakeholders.
- Lead audit and inspection readiness across regions, preparing and presenting data during regulatory audits and inspections.
- Develop responses to operations-related findings and drive timely implementation of corrective/preventive actions.
- Ensure team members are well-trained on pharmacovigilance processes and systems, with required competencies to fulfill responsibilities in changing business and regulatory environments.
- Maintain local pharmacovigilance procedures, ensuring alignment with local legislation, and provide pharmacovigilance strategic and operational expertise to team members.
- Implement consistent pharmacovigilance operational processes across regions, potentially serving as subject matter expert for assigned pharmacovigilance processes.
- Drive PV operations in compliance with local regulations, reviewing local legislation and partnering with Affiliate Safety Representatives to define impact on operational activities.
- Conduct regular operational review meetings with Affiliate Safety Representatives to communicate metrics and insights on health of Affiliate PV operations.
Qualifications:
- Minimum 5-7 years experience required within the pharmacovigilance field, including extensive experience in overseeing PV operational and compliance metrics.
- Advanced scientific degree (e.g., PhD, PharmD, MD) with prior experience leading small to medium-sized teams.
- Minimum 3-4 years with direct people management experience for medium to large teams.
- Demonstrated understanding of complexities and success measures of working in a global highly matrix environment.
- Experience in implementing and delivering transformation programs, proven leadership skills to lead and influence cross-functional matrix teams.
- Strong effective communicator and ability to influence across the enterprise, partnering and building strong relationships, and role-modeling leadership behaviors.
Key Stakeholders:
Senior Pharmacovigilance Specialist
Posted today
Job Viewed
Job Description
About Us:
This role is an exciting opportunity to join a dynamic team where you will be working closely with in-country partner functions to carry out and monitor local pharmacovigilance activities.
You will establish and implement processes compliant with regional/local PV regulations and global procedures, documenting them in local quality documents as appropriate.
The successful candidate will manage local compliance metrics, conduct root cause analysis (RCA), and implement corrective and preventive actions (CAPAs).
In addition, the role involves ensuring inspection readiness of the local PV system, maintaining an auditable trail of all PV activities and coordinating with stakeholders such as quality, medical, and regulatory teams.
Furthermore, the associate will review national regulations and communicate updates or new PV regulations to relevant stakeholders via the Regulatory Intelligence unit.
Key Responsibilities:
- Collaborate with in-country partner functions to carry out and monitor local PV activities.
- Establish and implement processes compliant with regional/local PV regulations and global procedures.
- Manage local compliance metrics, conduct RCA, and implement CAPAs.
Requirements:
To be successful in this role, you should have experience with pharmacovigilance systems and safety-related product management in clinical development and marketed products.
A minimum of experience in pharmacovigilance, regulatory affairs, quality, medical, or clinical development is required.
You should possess diplomacy, teamwork, cultural awareness, professionalism, and mediation skills, as well as problem-solving skills, sense of urgency, and ability to work under pressure.
What We Offer:
This company offers a unique opportunity to be part of a pioneering biopharma company where patient insights influence drug development.
You will work with AI-powered science that accelerates discovery and improves outcomes, collaborate with diverse, multidisciplinary teams to spark new ideas, and join a workplace committed to diversity, equity, and inclusion.
This company's Work Abroad Program offers roles with real responsibilities and growth opportunities across functions such as marketing, finance, regulatory, supply chain, clinical trials, production, and more in over 40 countries.
About You:
You should hold a Medical Doctor, Pharmacist, Pharm D, Veterinary Doctor, Health Sciences PhD, MPH, or a Master's degree in a related field.
Proficiency in English (verbal and written) is required, and knowledge of Arabic is a plus.
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