Company · 30 open roles
Careers at Excelya
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30 positions at Excelya
Data Manager VITRO
Excelya·Saclay, Île-de-France, France
Data Manager VITRO at Excelya. Location: Saclay, Île-de-France, France. Role: collecting requirements, testing VITRO, ensuring compliance Requirements: Minimum 5 years in data management (preclinical preferred), Master’s in a scientific/technical field, strong analytical and comm…
Freelance Senior Medical Writer
Excelya·Poland or Europe
Freelance Senior Medical Writer at Excelya. Location: Poland or Europe. Role: writing deliverables, coordinating stakeholders, ensuring compliance Requirements: Degree in life sciences, 3+ years medical writing experience producing protocols, CSRs, CTDs, ICFs and lay summaries, E…
Freelance Senior Medical Writer
Excelya·Bulgaria or Europe
Freelance Senior Medical Writer at Excelya. Location: Bulgaria or Europe. Role: writing deliverables, coordinating stakeholders, mentoring writers Requirements: Degree in life sciences, 3+ years medical writing experience, experienced in protocols/CSRs/CTDs/ICFs/lay summaries, fl…
Freelance Senior Medical Writer
Excelya·Romania or Europe
Freelance Senior Medical Writer at Excelya. Location: Romania or Europe. Role: writing deliverables, coordinating stakeholders, mentoring writers Requirements: Degree in life sciences,3+ years medical writing experience,experience with protocols,CSRs,CTDs,ICFs and lay summaries,E…
Freelance Senior Medical Writer
Excelya·Hungary or Europe
Freelance Senior Medical Writer at Excelya. Location: Hungary or Europe. Role: writing deliverables, coordinating stakeholders, mentoring writers Requirements: Degree in life sciences,3+ years medical writing experience producing protocols, CSRs, CTDs, ICFs and lay summaries; flu…
Local Safety Partner
Excelya·Paris, Île-de-France, France
Local Safety Partner at Excelya. Location: Paris, Île-de-France, France. Role: monitoring safety, assessing risks, supporting stakeholders Requirements: Degree in Medicine/Pharmacy/Life Sciences, solid pharmacovigilance experience, knowledge of PV regulations and risk management,…
Senior Regulatory Intelligence & AI
Excelya·Boulogne-Billancourt, Île-de-France, France
Senior Regulatory Intelligence & AI at Excelya. Location: Boulogne-Billancourt, Île-de-France, France. Role: identifying opportunities, analyzing sources, developing strategy Requirements: Pharmacist or life-sciences graduate with regulatory affairs experience and regulatory inte…
Global Quality Systems Coordinator
Excelya·Boulogne-Billancourt, Île-de-France, France
Global Quality Systems Coordinator at Excelya. Location: Boulogne-Billancourt, Île-de-France, France. Role: defining QMS, supporting audits, managing documentation Requirements: Scientific degree and strong experience in QMS and GxP compliance, audits/inspection readiness, CAPA a…
Clinical Research Associate Oncology
Excelya·Paris, Île-de-France, France
Clinical Research Associate Oncology at Excelya. Location: Paris, Île-de-France, France. Role: conducting visits, ensuring compliance, monitoring safety Requirements: Experienced CRA (oncology preferred); bachelor’s in life sciences, nursing, pharmacy or related; clinical researc…
Regulatory Affairs Manager
Excelya·Athens, Attica, Greece
Regulatory Affairs Manager at Excelya. Location: Athens, Attica, Greece. Role: providing guidance, supporting inspections, assessing risks Requirements: Proven regulatory affairs experience in clinical research/pharmaceuticals; strong knowledge of Greek clinical trial regulations…
Technicien(ne) de Production pharmaceutique
Excelya·Lyon, Auvergne-Rhône-Alpes, France
Technicien(ne) de Production pharmaceutique at Excelya. Location: Lyon, Auvergne-Rhône-Alpes, France. Role: ensuring compliance, documenting production, operating equipment Requirements: Degree in a scientific production field (Bac+3/5), pharmaceutical manufacturing experience, k…
Clinical Scientist Immunology
Excelya·France or Europe
Clinical Scientist Immunology at Excelya. Location: France or Europe. Role: supporting studies, reviewing data, drafting responses Requirements: Advanced degree in medicine/pharmacy/life sciences, strong clinical scientist experience, immunology/inflammation or oncology study exp…
Study Team Leader
Excelya·Saclay, Île-de-France, France
Study Team Leader at Excelya. Location: Saclay, Île-de-France, France. Role: leading teams, managing vendors, overseeing trials Requirements: Degree in life sciences, strong experience in clinical operations as a global clinical trial manager, proven leadership on international P…
Infirmier(e) de recherche clinique
Excelya·Boulogne-Billancourt, Île-de-France, France
Infirmier(e) de recherche clinique at Excelya. Location: Boulogne-Billancourt, Île-de-France, France. Role: conducting studies, performing procedures, coordinating visits Requirements: State RN diploma required; clinical research or pulmonology/hospital experience preferred; know…
Communication Manager EXT
Excelya·Dilbeek, Flanders, Belgium
Communication Manager EXT at Excelya. Location: Dilbeek, Flanders, Belgium. Role: creating content, designing plans, monitoring performance Requirements: Experience in communications or digital marketing (ideally in regulated pharma/healthcare), content creation across channels, …
Senior Medical Writer
Excelya·Bengaluru, Karnataka, India
Senior Medical Writer at Excelya. Location: Bengaluru, Karnataka, India. Role: writing deliverables, coordinating stakeholders, mentoring writers Requirements: University graduate in life sciences, advanced English, strong knowledge of ICH/CONSORT/STROBE/PRISMA, analytical skills…
Medical Writer
Excelya·Bengaluru, Karnataka, India
Medical Writer at Excelya. Location: Bengaluru, Karnataka, India. Role: drafting documents, reviewing documents, ensuring compliance Requirements: University graduate in life sciences, English fluency, strong knowledge of ICH, CONSORT, STROBE, PRISMA; analytical, detail-oriented,…
Clinical Study Assistant
Excelya·Leuven, Flemish Brabant, Belgium
Clinical Study Assistant at Excelya. Location: Leuven, Flemish Brabant, Belgium. Role: supporting trials, maintaining tmf, coordinating vendors Requirements: Bachelor in life sciences/nursing/pharmacy (or equivalent), up-to-date ICH-GCP, 2–5 years clinical research experience (CT…
Clinical Trial Assistant
Excelya·Paris, Île-de-France, France
Clinical Trial Assistant at Excelya. Location: Paris, Île-de-France, France. Role: providing support, managing tmf, coordinating communication Requirements: Bachelor's/Master's in life sciences or pharmacy required; strong clinical research experience; knowledge of clinical trial…
Clinical Research Associate
Excelya·Paris, Île-de-France, France
Clinical Research Associate at Excelya. Location: Paris, Île-de-France, France. Role: conducting visits, ensuring compliance, monitoring data Requirements: Experienced CRA with a bachelor's in life sciences, nursing, pharmacy or related; strong knowledge of clinical trial monitor…
eTMF Specialist
Excelya·Paris, Île-de-France, France
eTMF Specialist at Excelya. Location: Paris, Île-de-France, France. Role: managing eTMF, performing checks, monitoring metrics Requirements: Bachelor's or Master’s in health/life sciences, strong clinical trial documentation experience, hands-on Veeva Vault TMF, knowledge of DIA …
Chargé(e) Assurance Qualité Opérationnelle CMC
Excelya·Montpellier, Occitanie, France
Chargé(e) Assurance Qualité Opérationnelle CMC at Excelya. Location: Montpellier, Occitanie, France. Role: managing recalls, preparing inspections, coordinating investigations Requirements: Master's degree in a scientific field, confirmed experience in CMC development or quality …
Real World Evidence - Project Manager
Excelya·Dilbeek, Flanders, Belgium
Real World Evidence - Project Manager at Excelya. Location: Dilbeek, Flanders, Belgium. Role: leading studies, overseeing design, managing vendors Requirements: Expertise in real-world data and RWE methodologies, knowledge of Belgian healthcare and market access, ability to lead …
Clinical Scientist Oncologie
Excelya·Paris, Île-de-France, France
Clinical Scientist Oncologie at Excelya. Location: Paris, Île-de-France, France. Role: supporting trials, reviewing data, preparing documents Requirements: Advanced degree in life sciences required; strong analytical and clinical data review skills; familiarity with GCP and clini…