À propos de Diego
Key expertise:
• Signal detection & management (FDA/EMA/VAERS/EudraVigilance)
• ICSR case processing, PSUR/PBRER/RMP authoring & review
• GVP audits, CAPA, pharmacovigilance compliance
• Safety in vaccines, oncology, immuno-inflammatory diseases
• Pharmacovigilance support (case processing, signal assessment)
• PSUR/RMP writing & review
• GVP audits and inspection preparation
• Safety consulting for biotech/pharma
• Local Contact Person for PV (LCPPV)
Skills
Pharmacovigilance, Drug Safety, Signal Detection, Signal Management, ICSR, PSUR, PBRER, RMP, GVP, Pharma Compliance, Medical Affairs, Regulatory Affairs, Vaccines, Oncology, Immunology, Case Processing, GVP Audits, Risk Management, FDA, EMA, EudraVigilance, VAERS.
Now available as a freelance consultant for short- or long-term missions (remote):
Immediately available – flexible (part-time or full-time)
Feel free to reach out to discuss your needs. Quick response guaranteed.
Please visit my Linkedin profile to get the full idea on my career.
Français
Bilingue ou natif
Anglais
Bilingue ou natif
En télétravail uniquement
Travaille majoritairement à distance
Expériences
- GSKAssociate Medical Director, Safety Evaluation & Risk ManagementINDUSTRIE PHARMACEUTIQUEjuillet 2022 - mars 2026 (3 ans et 8 mois)Wavre, BW, Belgium• Led global pharmacovigilance and safety signal management strategies for assigned products.• Performed benefit-risk assessments and aggregate safety data reviews, ensuring compliance with regulatory requirements.• Drove cross-functional collaboration with Regulatory Affairs, Clinical Development, and Medical Affairs to align safety communications and strategies.• Prepared and review safety sections of clinical and regulatory documents, including study protocols, IBs, CSRs, and ICFs.• Led periodic safety report preparation (PSURs, DSURs) and safety submissions for global regulatory agencies.• Provided safety leadership for Data Safety Monitoring Boards (DSMBs) and internal safety governance.• Oversaw medical assessments of individual case safety reports (ICSRs) and ensure timely reporting of SUSARs and urgent safety issues.
- GSKSenior Manager Safety Physician, Safety Evaluation & Risk ManagementINDUSTRIE PHARMACEUTIQUEnovembre 2018 - juin 2022 (3 ans et 7 mois)Wavre, BW, Belgium• • Chaired Safety Review Team (SRT) meetings, leading discussions on benefit-risk evaluations.• • Authored and reviewed key safety documents, including PSURs, DSURs, RMPs, and regulatory responses.• • Provided medical oversight for safety sections in clinical trial documentation (protocols, CSRs, IBs, and ICFs).• • Led safety discussions with regulatory agencies and participated in IDMC/DSMB meetings.
- GSKVaccines Medical Affairs ManagerINDUSTRIE PHARMACEUTIQUEdécembre 2015 - février 2018 (2 ans et 2 mois)Kinshasa, KN, Democratic Republic of Congo• Provided medical and scientific leadership in vaccine safety and risk management.• Engaged with Key Opinion Leaders (KOLs) and healthcare professionals to support vaccine education and advocacy.• Managed regional pharmacovigilance strategies, strengthening regulatory compliance in Central Africa.
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Formations
- Executive MasterUniversity of Siena & Novartis Vaccines Academy2014Executive Master
- Doctor of Medicine (MD)University of Kinshasa2010Doctor of Medicine (MD)