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Excelya is seeking a Regulatory Affairs professional to manage marketing authorization activities for veterinary medicines across France and Europe within its clinical research organization.
Excelya is hiring a Biostatistician to support clinical research by designing and analyzing clinical trials and contributing statistical expertise to decision-making and regulatory submissions.
Excelya is seeking a Senior CMC Regulatory Technical Writer to produce compliant CTD documentation for Phase 3 and Marketing Authorization submissions in close collaboration with CMC and cross-functional technical teams.
Excelya is hiring a Local Responsible Person for Pharmacovigilance (LRPV) in APAC to oversee local safety operations, regulatory compliance, and stakeholder coordination within its PV & Safety team.
Excelya is seeking a part-time Local Regulatory Affairs Expert in Malta to provide consultancy and support for pharmaceutical marketing authorizations and ongoing regulatory compliance.
Senior Safety Officer at Excelya joining the Pharmacovigilance and Safety team to lead the compilation, authoring, and coordination of aggregate periodic safety reports and safety evaluations to meet global regulatory requirements.
