- Firma:
Accenture (zaměstnavatel)
- Místo pracoviště:
Plynární 1617/10, Praha - Holešovice
Ukázat na mapě - Pracovní poměr:práce na plný úvazek
- Smluvní vztah:pracovní smlouva
- Vzdělání:bakalářské
- Jazyky:angličtina (výborná)
- Zařazení:farmaceut, medical advisor, vedoucí/manažer lékárny, věda a výzkum, zdravotnictví a sociální péče, farmacie
Co říká Accenture o pozici
Accenture is a leading global professional services company, providing a broad range of services and solutions in strategy, consulting, digital, technology and operations. Combining unmatched experience and specialized skills across more than 40 industries and all business functions – underpinned by the world’s largest delivery network – Accenture works at the intersection of business and technology to help clients improve their performance and create sustainable value for their stakeholders. With more than 730,000 people serving clients in more than 120 countries, Accenture drives innovation to improve the way the world works and lives.
Job Description
The Drug Safety Team Lead is responsible for overseeing pharmacovigilance (PV) activities to ensure the safety of patients and compliance with global regulatory requirements. This role provides strategic and operational leadership for safety surveillance across clinical development and post-marketing products. The Drug Safety Team Lead collaborates cross-functionally with Clinical Operations, Regulatory Affairs, Medical Affairs, Quality Assurance, and external partners to ensure high-quality safety reporting and risk management.
Responsibilities/Authorities
- Lead and manage the Drug Safety team, including safety scientists and case processing staff.
- Provide strategic oversight for safety surveillance activities across clinical trials and marketed products.
- Serve as the safety representative on cross-functional project teams.
- Develop and implement pharmacovigilance strategies aligned with company and regulatory requirements.
- Ensure compliance with global pharmacovigilance regulations (FDA, EMA, ICH guidelines, and other regional authorities).
- Maintain inspection readiness and support regulatory audits and inspections.
- Review and approve safety documentation and regulatory submissions
- Job QualificationsJob Qualifications
- Educational and Experience Requirements
- MD, PharmD, PhD, or Master’s degree in life sciences, pharmacy, nursing, or related field.
- 5+ years of experience in pharmacovigilance or drug safety.
- 3+ years of leadership or team management experience preferred.
We offer:
Recognition:
- Flexible Benefit System - budget to be spent on services of your choice
- Competitive bonus structure
- Refer-a-Friend – get a bonus in the employee referral program
- Loyalty rewards
Future:
- Wide range of trainings and expert lectures
- Employee share purchase plan
- Pension / Life insurance contribution
Leisure & Health:
- 5 extra days off
- Sick leave salary compensation
- Employee assistance services (professional psychological, financial and legal help)
- Multisport card
Almost a match?
Don’t worry - apply anyway! We value potential just as much as experience.
Benefity
- Bonuses
- Notebook
- Contributions to the pension / life insurance
- Meal tickets / catering allowance
- Holidays 5 weeks
- Educational courses, training
- Cafeteria
- Refreshments on workplace
- Contribution to sport / culture / leisure
- Sick days
- Occasional work from home
- Corporate events