Excelya, founded in 2014 and headquartered in Paris, is an independent partner that delivers full‑service clinical research, regulatory, and resourcing solutions to biotech, pharma, and medical‑device companies worldwide. With a global footprint spanning 28 countries and a team of more than 900 experts, the firm customizes trial operations across a broad therapeutic spectrum, concentrating on oncology, rare disease, pediatrics, infectious disease, immuno‑oncology, pain, CNS, and real‑world evidence. Excelya’s distinct value lies in its compassionate, data‑driven approach that blends regulatory expertise, biometrics, medical writing, and pharmacovigilance to accelerate late‑phase development. The company’s culture emphasizes excellence, collaboration, and client‑centric innovation, positioning it as a trusted partner in the life‑science research ecosystem.
Open Positions
Senior CMC Regulatory Technical Writer
10 years of CMC experience, strong writing and organizational skills, regulatory knowledge
International Clinical Operations Lead
Proven international clinical operations experience, strong organizational skills, and fluency in French and English
Pharmacovigilance Officer
Doctor of Pharmacy (PharmD) degree required, with experience in managing CAPAs, deviations, and regulatory compliance indicators
Senior Associate Clinical Contracts & Budgets
At least 2 years of experience in clinical contracts and budget management, mandatory experience in negotiating contracts under the French Convention Unique framework, Master's degree in Law, Finance, Business, Life Sciences, or related field
Ingénieur(e) biomédical dispositif Médical
Biomedical engineer or Bac+5 in biomedical, experience in medical device implantable Class III biocompatibility validation, mastering of ISO 10993 and ISO 13485 quality systems, good knowledge of MDR (EU 2017/745), fluent in French and English
Biostatistician
3+ years of experience in biostatistics, proficiency in statistical software, and a Master's degree in Biostatistics or related field
Safety Officer
University degree in Life Sciences, 2+ years of pharmacovigilance experience, and proficiency in MS Office and safety databases
Epidemiologist
Proven experience in clinical operations, experience as Clinical Research Associate, Master's degree in related field
Safety Database Officer
3+ years Pharmacovigilance experience, pharmacovigilance database proficiency, Life Sciences degree, and English fluency
Senior Business Unit Manager
Proven experience as a Business Manager Lead, team leadership, commercial development, and consultant management
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