Join our trailblazing team as a Drug Safety Manager, where you'll lead the charge in pharmacovigilance project management and inspire a team dedicated to advancing in patient safety.
Main responsibilities :
Elevate Patient Safety & Lead with Excellence as a Drug Safety Manager, you will orchestrate a symphony of vigilance, ensuring that every note of our pharmacovigilance projects resonates with precision and care. Your expertise will be the beacon guiding our team through of :
- Weekly global and local literature review : Conducting meticulous weekly literature reviews, both globally and locally, to stay ahead of safety insights.
- Case Management : Mastering the handling of Individual Case Safety Reports (ICSRs) and diligent follow-ups, safeguarding patient well-being.
- Management Global Safety Database : Streamlining the processing of cases through our own database, ensuring every detail is captured.
- EudraVigilance Reporting : Reporting cases to European authorities with accuracy and efficiency.
- Communication with Competent Authorities : Engaging with Competent Authorities, serving as a pivotal point of contact.
- Regulatory Intelligence : Keeping our clients and company abreast of the evolving global and local pharmacovigilance legislation and authority requirements.
- PSMF and PV SOPs : Overseeing the maintenance of the PSMF and Asphalion's robust Pharmacovigilance System (SOPs).
- PV Audits : Conducting thorough pharmacovigilance audits, ensuring compliance and maintaining the integrity of client’s PV system.
- EU-QPPV and local person for PV in Spain Support : Providing unwavering support to the EU-QPPV and local person for PV in Spain, ensuring the highest standards of patient safety across the European Union.
- Aggregate Safety Reports : Crafting comprehensive Periodic Safety Update Reports (PSURs), Risk Management Plans (RMP), ACOs, DSUR.
- Medical Advisory : Providing insightful advice, shaping the efficiency in drug safety.
- PV Agreements : Drafting meticulous Pharmacovigilance contracts that set the standard for collaboration.
Requirements :
5 years experience in Pharmacovigilance departments.2 years experience in Team Management & Project ManagementFluent in English & Spanish
Previous experience working in an international environment
Academic Degree in Life Science and Pharmacovigilance.
Advanced IT level – (MS Office)
Proactive, good communication, accurate, detail orientated
Why working at Asphalion?
Permanent contract.
Flexible working schedule - Friday until 15.30h.
Homeoffice & Hybrid or Remote Model (You can be located anywhere in Spain!)
Wide variety of projects, new challenges and experiences.
Training and personal development program.
English lessons.
A professional, inclusive and high-performance work environment to develop your skills and grow your career. A great company culture built around Passion, Flexibility, Commitment, Quality & Companionship.
A highly & dynamic working environment with employees from more than 15 nationalities.
Our people and their well-being are our priority : Physical, psychological and emotional well-being programme.
Internal activities & RSC Activities
Equal Opportunity Employee