Emplois actuels liés à Clinical Trial Assistant - France - Excelya
-
Clinical Trial Leader F/H
Il y a 3 mois
France Excelya Temps pleinPrésentation :Excelya Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care. We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 900 Excelyates. Our unique one-stop provider service model –...
-
Clinical Trial Leader F/H
Il y a 3 mois
France, FR Excelya Temps pleinPrésentation :Excelya Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care. We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 900 Excelyates. Our unique one-stop provider service model –...
-
Clinical Trial Assistant
Il y a 2 mois
France Excelya Temps pleinCreated in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care.We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 900 Excelyates. Our unique one-stop provider service model – leveraging full-service,...
-
Clinical Trial Assistant
Il y a 2 mois
France, FR Excelya Temps pleinCreated in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care.We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 900 Excelyates. Our unique one-stop provider service model – leveraging full-service,...
-
Senior Clinical Research Associate
il y a 2 jours
France, FR AL Solutions Temps pleinChloe O'Shea has a brand new and fantastic opportunity for Senior CRA's in the France! Chloe is working with a global CRO who are looking for dedicated Senior CRA's to join their close-knit team!!About the role: The successful candidate will have lots of autonomy and will have a lot of say in the clinical trials so you must be a confident CRA!...
-
Senior Clinical Research Associate
il y a 2 jours
France AL Solutions Temps pleinChloe O'Shea has a brand new and fantastic opportunity for Senior CRA's in the France! Chloe is working with a global CRO who are looking for dedicated Senior CRA's to join their close-knit team!!About the role: The successful candidate will have lots of autonomy and will have a lot of say in the clinical trials so you must be a confident CRA!...
-
Senior Clinical Research Associate
Il y a 2 mois
France Parexel Temps pleinParexel is currently seeking Senior Clinical Research Associates in France. These will be home-based positions and fully dedicated to a single sponsor. Working as a Senior Clinical Research Associate at Parexel offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and...
-
Clinical Scientist
il y a 2 jours
Île-de-France Excelya Temps pleinI. Excelya Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care. We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 900 Excelyates. Our unique one-stop provider service model – leveraging...
-
Clinical Scientist
il y a 2 jours
Île-de-France, France Excelya Temps pleinI. Excelya Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care. We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 900 Excelyates. Our unique one-stop provider service model – leveraging...
-
Senior Clinical Research Associate
Il y a 2 mois
France Parexel Temps plein**We are looking for passionate professionals with solid experience as CRAs to work as Senior CRA for onsite monitoring visits in Chile** **Your time here** At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and...
-
Clinical Research Associate France
Il y a 2 mois
France ICON Plc Temps pleinClinical Research Associates - France ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. **CRA II or Senior CRA** **France, Office or...
-
Associate Director Biostatistics
il y a 2 jours
France, FR Warman O'Brien Temps pleinAssociate Director Biostatistics - Top Pharma - FranceOur client, a leading global pharma is looking for an expert biostatistician to join, their dynamic team, working on exciting projects in various therapeutic areas.PurposeProvide statistical expertise and contributions for projects and protocols in support of Drug Development ProgramsProvide statistical...
-
Associate Director Biostatistics
il y a 2 jours
France Warman O'Brien Temps pleinAssociate Director Biostatistics - Top Pharma - FranceOur client, a leading global pharma is looking for an expert biostatistician to join, their dynamic team, working on exciting projects in various therapeutic areas.PurposeProvide statistical expertise and contributions for projects and protocols in support of Drug Development ProgramsProvide statistical...
-
Senior Customer Success Engineer
il y a 2 jours
France Prelude Temps pleinDescriptionA Customer Success Engineer (CSE) at Prelude is pivotal in ensuring our clients' success and satisfaction with Prelude and our software products. A Prelude CSE’s primary responsibility is to ensure our clients' successful implementation, adoption, and ongoing satisfaction utilizing our platform. This includes guiding clients through our...
-
Senior Customer Success Engineer
il y a 2 jours
France, FR Prelude Temps pleinDescriptionA Customer Success Engineer (CSE) at Prelude is pivotal in ensuring our clients' success and satisfaction with Prelude and our software products. A Prelude CSE’s primary responsibility is to ensure our clients' successful implementation, adoption, and ongoing satisfaction utilizing our platform. This includes guiding clients through our...
-
Medical Affairs Specialist EMEA DBS
Il y a 2 mois
Île-de-France Boston Scientific Temps pleinAdditional Locations: France-Île-de-France; Germany-Düsseldorf; Italy-Milan; Spain-Madrid; United Kingdom-Hemel Hempstead Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and...
-
Biostatisticien Clinique
Il y a 4 mois
Île-de-France IT&M STATS Temps pleinIT&M Stats intervient dans le domaine des statistiques, de la programmation et de la data science, principalement dans les secteurs de l’Industrie Pharmaceutique, Cosmétique, dans la Santé et l’Agro-alimentaire et auprès des Banques et Assurances. IT&M Stats est une filiale du Groupe Astek, acteur mondial de l’ingénierie et du conseil en...
-
Biostatisticien Clinique
Il y a 4 mois
Île-de-France, France IT&M STATS Temps pleinIT&M Stats intervient dans le domaine des statistiques, de la programmation et de la data science, principalement dans les secteurs de l’Industrie Pharmaceutique, Cosmétique, dans la Santé et l’Agro-alimentaire et auprès des Banques et Assurances. IT&M Stats est une filiale du Groupe Astek, acteur mondial de l’ingénierie et du conseil en...
Clinical Trial Assistant
Il y a 2 mois
Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care.
We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 900 Excelyates. Our unique one-stop provider service model – leveraging full-service, functional service provider and consulting – allows our Excelyates to evolve through a diverse array of projects. In collaboration with preeminent experts, Excelya advances scientific, managerial and human knowledge to improve the patient journey.
For our team members, excelling with care means benefitting from a stimulating professional environment that encourages personal, intellectual, and operational participation so that together we can be the best in our field. We commit to giving each Excelyate the means to express their natural talents, develop their full potential and invest their unique selves in our unique project.
Mission :
- Support the clinical project management and monitoring of clinical studies, including liaison with, monitors, CROs, drug vendors, central laboratories and other vendors for study related tasks.
- Be an active member of the study team and take responsibilities for service provider oversight for his/her scope of responsibility according to procedures
- Be responsible for monitoring, verifying and archiving the Trial Master File as per SOPs, instructions and trainings. This includes review and QC check of the TMF to ensure quality and completeness in view of audit, inspection and archiving.
- Be responsible for follow up and review of financial documents, in collaboration with GCPM.
- Create and update financial information within financial systems (SAP, K2) as need be as per study progress and service provider contract modification (commitment request, Internal Order, Purchase order, goods receipt & invoices).
- Create and update financial trackers, follow up of invoices and delay in payments
- Help to prepare forecast and assist at quarterly review meetings of study budget with GCPM and local finance controlling department
Profile :
At least 3 years of work experience and training in clinical operations in a similar role. Substantial administrative experience or qualified to degree level.
• Fluent in English /Strong intermediate level Proficiency
• Basic Financial Knowledge
• Knowledge of regulatory documents or medical terminology is recommended.
• Experience of working with multidisciplinary groups and ability to work within a team environment.
• Experience of managing and developing relationships with international Service Providers (SPs).
• Experience of tracking and manipulating clinical study documents and provider invoices.
• Strong organizational and skills
• Excellent verbal and written communication skills.
