Redefine Clinical. Empower Innovation. Build with Audacity. Join Excelya as Our Next Clinical Operations Star! At Excelya, we don’t just work—we Excelyate. Across 24 countries, 900+ passionate professionals are shaping t…
Dans le cadre du renforcement des activités de recherche clinique en oncologie, nous recherchons un(e) Technicien(ne) d'Études Cliniques (TEC) pour contribuer à la gestion et à la qualité des données cliniques issues des…
Skills: Data Entry, eCRF Tools, Good Clinical Practice (GCP), Clinical Data Management, Source Document Review
RegCMC consultant with drug substance development experience
Saclay, Ile-de-France, France · On-site
Senior
About the Job At Excelya, where Audacity, Care, and Energy are at the core of everything we do, we are seeking a CMC Regulatory Consultant specializing in drug substance lifecycle management to join our dynamic team. Thi…
Redefine Medical. Empower Innovation. Build with Audacity. Join Excelya as Our Next Medical Star! At Excelya, we don’t just work—we Excelyate. Across 24 countries, 900+ passionate professionals are shaping the future of …
Skills: Medical Writing, Clinical Study Reports, Clinical Evaluation Reports, CTD Submissions, Protocol Writing
Boulogne-Billancourt, Ile-de-France, France · Hybrid
Mid level
Redefine Medical. Empower Innovation. Build with Audacity. Join Excelya as Our Next Medical Star! At Excelya, we don’t just work—we Excelyate. Across 24 countries, 900+ passionate professionals are shaping the future of …
Skills: Medical Writing, Clinical Study Reports, Clinical Evaluation Reports, CTD Submissions, Protocol Writing
Redefine Medical. Empower Innovation. Build with Audacity. Join Excelya as Our Next Medical Star! At Excelya, we don’t just work—we Excelyate. Across 24 countries, 900+ passionate professionals are shaping the future of …
Skills: Medical Writing, Clinical Study Reports, Clinical Evaluation Reports, CTD Submissions, Protocol Writing
Redefine Medical. Empower Innovation. Build with Audacity. Join Excelya as Our Next Medical Star! At Excelya, we don’t just work—we Excelyate. Across 24 countries, 900+ passionate professionals are shaping the future of …
Skills: Medical Writing, Clinical Study Reports, Clinical Evaluation Reports, CTD Submissions, Protocol Writing
Redefine Medical. Empower Innovation. Build with Audacity. Join Excelya as Our Next Medical Star! At Excelya, we don’t just work—we Excelyate. Across 24 countries, 900+ passionate professionals are shaping the future of …
Skills: Medical Writing, Clinical Study Reports, Clinical Evaluation Reports, CTD Submissions, Protocol Writing
Redefine Medical. Empower Innovation. Build with Audacity. Join Excelya as Our Next Medical Star! At Excelya, we don’t just work—we Excelyate. Across 24 countries, 900+ passionate professionals are shaping the future of …
Skills: Medical Writing, Clinical Study Reports, Clinical Evaluation Reports, CTD Submissions, Protocol Writing
Join Excelya, a company driven by Audacity, Care, and Energy, where innovation and collaboration are at the heart of everything we do. As a QMS Support Manager, you will support a strategic site transformation project by…
Senior Consumer Engagement & Digital Marketing Consultant
Dilbeek, Flanders, Belgium · Hybrid
Senior+
Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. Ma…
Skills: Consumer Engagement, Digital Marketing, Omnichannel Strategy, SEO, GEO
Join Excelya, a company driven by Audacity, Care, and Energy, where innovation and collaboration are at the heart of everything we do. As a Global Clinical Project Manager, you will be responsible for leading global clin…
Join Excelya, a company driven by Audacity, Care, and Energy, where innovation and collaboration are at the heart of everything we do. As a QMS Quality Manager, you will support a strategic site transformation project by…
Redefine Medical. Empower Innovation. Build with Audacity. Join Excelya as Our Next Medical Star! At Excelya, we don’t just work—we Excelyate. Across 24 countries, 900+ passionate professionals are shaping the future of …
Skills: Medical Writing, Clinical Study Reports, Clinical Evaluation Reports, CTD Submissions, Informed Consent Forms
Redefine Medical. Empower Innovation. Build with Audacity. Join Excelya as Our Next Medical Star! At Excelya, we don’t just work—we Excelyate. Across 24 countries, 900+ passionate professionals are shaping the future of …
Skills: Medical Writing, Clinical Study Reports, Clinical Evaluation Reports, CTD Submissions, Informed Consent Forms
Redefine Medical. Empower Innovation. Build with Audacity. Join Excelya as Our Next Medical Star! At Excelya, we don’t just work—we Excelyate. Across 24 countries, 900+ passionate professionals are shaping the future of …
Skills: Medical Writing, Clinical Study Reports, Clinical Evaluation Reports, CTD Submissions, Informed Consent Forms
Redefine Medical. Empower Innovation. Build with Audacity. Join Excelya as Our Next Medical Star! At Excelya, we don’t just work—we Excelyate. Across 24 countries, 900+ passionate professionals are shaping the future of …
Skills: Medical Writing, Clinical Study Reports, Clinical Evaluation Reports, CTD Submissions, Informed Consent Forms
Redefine Medical. Empower Innovation. Build with Audacity. Join Excelya as Our Next Medical Star! At Excelya, we don’t just work—we Excelyate. Across 24 countries, 900+ passionate professionals are shaping the future of …
Skills: Medical Writing, Clinical Study Reports, Clinical Evaluation Reports, CTD Submissions, Informed Consent Forms
Redefine Medical. Empower Innovation. Build with Audacity. Join Excelya as Our Next Medical Star! At Excelya, we don’t just work—we Excelyate. Across 24 countries, 900+ passionate professionals are shaping the future of …
Skills: Medical Writing, Clinical Study Reports, Clinical Evaluation Reports, CTD Submissions, Informed Consent Forms
Boulogne-Billancourt, Ile-de-France, France · Hybrid
Senior
At Excelya, driven by Audacity, Care, and Energy, we invite you to join our team as a Clinical Quality Manager. This pivotal role focuses on overseeing the quality management system within clinical operations to ensure c…
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Full-time
bachelor degree
Posted 19d ago
~40 hrs/week
Responsibilities
The role involves managing the administrative and logistical aspects of clinical trials, including regulatory submissions to Ethics Committees and Authorities. Key duties include maintaining the Trial Master File (TMF), tracking site activation, and coordinating with sponsors and vendors.
Requirements
Candidates must hold a degree in Life Sciences and have 1-2 years of experience in clinical trials. Proficiency in English, advanced Excel skills, and a strong understanding of ICH-GCP guidelines are required.
Full job description
Redefine Clinical. Empower Innovation. Build with Audacity.
Join Excelya as Our Next Clinical Operations Star!
At Excelya, we don’t just work—we Excelyate. Across 24 countries, 900+ passionate professionals are shaping the future of healthcare with one bold ambition: to become Europe's leading mid-size CRO, offering the best employee experience.
Now, we’re calling on curious minds and courageous spirits to step into a career-defining role in Clinical Operations. Ready to make an impact that travels the globe? Let’s talk.
About the Job
We are seeking a Study Start Up Specialist / Clinical Trial Assistant (SSUS/CTA), to provide clinical and scientific expertise required for the successful completion of Excelya’s projects.
The SSUS/CTA supports the project teams in administration, maintenance and coordination of all logistical aspects of clinical trials, according to ICH-GCP guidelines and applicable Standard Operating procedures (SOPs). The SSUS/CTA reports to the Line Manager and works closely with the responsible team for the project concerned in order to contribute to the effective and timely accomplishment of all logistical and administrative issues relevant to clinical projects.
Your Mission:
Clinical trial application preparation and submission to Ethics Committees and Regulatory Authorities.
Coordination and tracking of study start-up activities through site activation.
Collection, review, and maintenance of essential regulatory and site documents.
Management of investigator contracts, budgets, and study-related financial activities.
Maintenance of TMF, study trackers, and sponsor/regulatory documentation.
Collaboration with sponsors, sites, vendors, and cross-functional project teams to ensure timely study start-up.
What You Bring to the Table:
We are looking for candidates who embody our values of Audacity, Care, and Energy and also:
Degree in Life Sciences.
1-2 years of experience in clinical trials is required.
Good communication and organizational skills.
Ability in handling documents and good writing ability.
Time management & commitment to results, attention to detail, self-motivated and able to work both independently and within teams.
Ability to work with little supervision and self-confidence.
Excellent MS Office and advanced Excel skills.
Fluency in English.
Why Choose Excelya?
At Excelya, we lead with Audacity, act with Care, and move with Energy. We nurture your potential through high-impact projects, give your talents the space to shine, and push boundaries to elevate every patient’s journey. Here, you're not just doing a job—you’re becoming a key part of something bigger.
So, if you're ready to excel with purpose, let’s write the next chapter together.
Expertly delivering clinical trials operations, with care.
Industry
Pharmaceutical Manufacturing
Company size
501-1,000 employees
Founded
2014
Headquarters
Boulogne-Billancourt, Île-de-France
LinkedIn followers
114,770
Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of Full-service CRO, FSP, and Resourcing solutions guided by Energy, Care, and Audacity.
Founded in 2014 and headquartered in Paris, France, and operating in 28 countries across Europe, USA and India, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas, with speciality focus on Oncology & Hematology, Rare Disease & Pediatrics, Infectious Disease, Inflammation & Immunotherapy, Pain Treatment & CNS, and Late Phase & RWE.
Offices: 35, Rue de Paris, Boulogne-Billancourt, Île-de-France 92100, FR · 58 Pindou Street, Nea Filadelfia, Athens, GR · The Millenia Nos 1 & 2 Murphy Road Ulsoor,, Bangalore Karnataka, 560008, IN · 19 bd Eugène Deruelle, Lyon, 69003, FR · 1 Quai du Président Wilson, Bègles, Bordeaux 33130, FR
Opérations cliniquesAffaires RéglementairesBiométrieRédaction MédicalePharmacoviglanceInformation MédicaleContract Research OrganisationBiometrics and Clinical ResearchData ManagementPharmacovigilance
Expertly delivering clinical trials operations, with care.
Industry
Pharmaceutical Manufacturing
Company size
501-1,000 employees
Founded
2014
Headquarters
Boulogne-Billancourt, Île-de-France
LinkedIn followers
114,770
Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of Full-service CRO, FSP, and Resourcing solutions guided by Energy, Care, and Audacity.
Founded in 2014 and headquartered in Paris, France, and operating in 28 countries across Europe, USA and India, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas, with speciality focus on Oncology & Hematology, Rare Disease & Pediatrics, Infectious Disease, Inflammation & Immunotherapy, Pain Treatment & CNS, and Late Phase & RWE.
Offices: 35, Rue de Paris, Boulogne-Billancourt, Île-de-France 92100, FR · 58 Pindou Street, Nea Filadelfia, Athens, GR · The Millenia Nos 1 & 2 Murphy Road Ulsoor,, Bangalore Karnataka, 560008, IN · 19 bd Eugène Deruelle, Lyon, 69003, FR · 1 Quai du Président Wilson, Bègles, Bordeaux 33130, FR
Opérations cliniquesAffaires RéglementairesBiométrieRédaction MédicalePharmacoviglanceInformation MédicaleContract Research OrganisationBiometrics and Clinical ResearchData ManagementPharmacovigilance