Emplois actuels liés à Clinical Trial Manager - Paris, Île-de-France - Amgen
-
Clinical Trials Project Manager
il y a 1 mois
Paris, Île-de-France Worldwide Clinical Trials, LLC Temps pleinAbout Worldwide Clinical Trials Worldwide Clinical Trials (Worldwide) is a premier global contract research organization (CRO) that collaborates with biotechnology and pharmaceutical firms to develop tailored solutions that propel new medications from concept to reality. The Role of Project Management at Worldwide At Worldwide Clinical Trials, our Project...
-
Clinical Trials Manager
il y a 5 heures
Paris, Île-de-France Parexel Temps pleinInvestigator Contracts Lead (ICL) Job DescriptionParexel FSP is seeking an experienced Investigator Contracts Lead (ICL) to join our team in France.Key Responsibilities:Negotiate and manage contracts with clinical investigator sites, including initial agreements and amendments.Oversee the Per-Subject Cost (PSC) process for assigned studies and manage...
-
Clinical Trials Manager
il y a 5 heures
Paris, Île-de-France Parexel Temps pleinInvestigator Contracts Lead (ICL) Job DescriptionParexel FSP is seeking a highly skilled Investigator Contracts Lead (ICL) to join our team in France.Key Responsibilities:Negotiate and manage contracts with clinical investigator sites, ensuring timely and cost-effective execution.Collaborate with Legal and other divisions to manage escalations and identify...
-
Clinical Trial Coordinator
il y a 2 semaines
Paris, Île-de-France Excelya Temps pleinAbout the RoleWe are seeking a highly organized and detail-oriented Clinical Trial Assistant to join our team at Excelya. As a Clinical Trial Assistant, you will play a crucial role in supporting the clinical trials secretariat of a pharmaceutical laboratory.Key ResponsibilitiesManage and maintain clinical trial documents in VeevaVault eTMF, ensuring...
-
Clinical Trials Strategist
il y a 2 jours
Paris, Île-de-France Excelya Temps pleinClinical Trials Strategist **About Excelya** Excelya is a people-centered Contract Research Organization (CRO) that excels with care. Our team members benefit from a stimulating professional environment that encourages personal, intellectual, and operational participation. **Job Description** As a Clinical Trials Strategist, you will actively contribute...
-
Clinical Trials Strategist
il y a 2 jours
Paris, Île-de-France Excelya Temps pleinClinical Trials Strategist **About Excelya** Excelya is a people-centered Contract Research Organization (CRO) that excels with care. Our team members benefit from a stimulating professional environment that encourages personal, intellectual, and operational participation. **Job Description** As a Clinical Trials Strategist, you will actively contribute...
-
Clinical Trials Strategist
il y a 2 jours
Paris, Île-de-France Excelya Temps pleinClinical Trials Strategist **About Excelya** Excelya is a people-centered Contract Research Organization (CRO) that excels with care. Our team members benefit from a stimulating professional environment that encourages personal, intellectual, and operational participation. **Job Description** As a Clinical Trials Strategist, you will actively contribute...
-
Clinical Trials Strategist
il y a 2 jours
Paris, Île-de-France Excelya Temps pleinClinical Trials Strategist **About Excelya** Excelya is a people-centered Contract Research Organization (CRO) that excels with care. Our team members benefit from a stimulating professional environment that encourages personal, intellectual, and operational participation. **Job Description** As a Clinical Trials Strategist, you will actively contribute...
-
Clinical Trials Coordinator
il y a 2 semaines
Paris, Île-de-France IQVIA Temps pleinJob SummaryThe Clinical Research Administrative Assistant will play a vital role in supporting the Clinical Research team at IQVIA. This position will be responsible for providing administrative support to the clinical teams, ensuring the smooth execution of clinical trials.Key ResponsibilitiesAssist Clinical Research Associates (CRAs) and Regulatory and...
-
Clinical Trials Coordinator
il y a 2 jours
Paris, Île-de-France Excelya Temps pleinJoin Excelya's Team as a Clinical Trials AssistantExcelya, a people-centered Contract Research Organization (CRO), is seeking a highly skilled Clinical Trials Assistant to join our team. As a Clinical Trials Assistant, you will play a crucial role in supporting the clinical project management and monitoring of clinical studies.Key Responsibilities:Support...
-
Clinical Trial Budget Manager
il y a 2 semaines
Paris, Île-de-France Parexel Temps pleinAbout the Role:The Investigator Contracts Lead (ICL) is a key member of our team at Parexel, responsible for negotiating and managing contracts with clinical trial sites in France. This role requires a strong understanding of clinical trial budgets and contracting principles, as well as excellent communication and negotiation skills.Key...
-
Clinical Trials Coordinator
il y a 4 jours
Paris, Île-de-France IQVIA Temps pleinJoin Our Team as a Clinical Research Administrative AssistantIQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are seeking a highly motivated and organized Clinical Research Administrative Assistant to join our team in France.Key Responsibilities:Provide...
-
Clinical Trial Activation Manager
il y a 2 semaines
Paris, Île-de-France Planet Pharma Temps pleinJob Summary: We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Planet Pharma. As a key member of our regulatory team, you will be responsible for ensuring the timely and quality delivery of site activation readiness within assigned countries/sites.Key Responsibilities:Prepare and submit Clinical Trial Application Forms and...
-
Clinical Trials Project Leader
il y a 1 mois
Paris, Île-de-France Next Phase Recruitment Temps pleinKey Responsibilities:Oversee and manage the execution of one or multiple clinical studies.Ensure that the project is always prepared for audits (including project team training documentation, central files, system validation, etc.).Administer the project(s) within the established budgets and timelines.Take charge of the selection, contracting, coordination,...
-
Senior Clinical Research Associate
il y a 2 semaines
Paris, Île-de-France Allucent Temps pleinAbout the RoleWe are seeking a highly experienced and skilled Senior Clinical Research Associate to join our team at Allucent. As a key member of our clinical operations team, you will play a critical role in ensuring the successful execution of clinical trials.Key ResponsibilitiesStudy Monitoring: Independently monitor and control investigational sites,...
-
Senior Clinical Research Associate
il y a 1 semaine
Paris, Île-de-France Allucent Temps pleinAbout the RoleWe are seeking a highly experienced and skilled Senior Clinical Research Associate to join our team at Allucent. As a key member of our clinical operations team, you will be responsible for independently controlling and monitoring investigational sites, detecting issues, and providing solutions to ensure clinical studies are performed according...
-
Pediatric Nurse
il y a 4 heures
Paris, Île-de-France Planet Pharma Temps pleinJob Title: Pediatric Nurse - Decentralized Clinical TrialsWe are seeking a highly skilled Pediatric Nurse to join our team for Decentralized Clinical Trials. As a Pediatric Nurse, you will be responsible for providing high-quality patient care and ensuring the smooth execution of clinical trials.Main Responsibilities:Provide patient care and support to...
-
Clinical Trial Operations Specialist
il y a 2 semaines
Paris, Île-de-France Excelya Temps pleinAbout the RoleWe are seeking a highly skilled and experienced Clinical Trial Operations Specialist to join our team at Excelya. As a key member of our clinical operations team, you will play a critical role in the management and coordination of clinical studies.Key ResponsibilitiesStudy Management: Support the clinical project management and monitoring of...
-
Clinical Trial Coordinator
il y a 7 jours
Paris, Île-de-France PSI Temps plein{"Job Title": "Site Coordinator", "Job Description": "Job OverviewThe Site Coordinator plays a critical role in supporting clinical trial activities at a medical institution or research center. This position requires strong communication and organizational skills to ensure seamless execution of study procedures and timely completion of tasks.Key...
-
Medical Director
il y a 1 semaine
Paris, Île-de-France INTERTEK Temps pleinJob SummaryWe are seeking a highly skilled Medical Director - Clinical Trials Investigator to join our team at Intertek. As a key member of our Business Line Chemicals & Pharmaceuticals, you will be responsible for leading clinical trials and ensuring the quality and safety of our products.Key ResponsibilitiesLead clinical trials and ensure compliance with...
Clinical Trial Manager
Il y a 4 mois
Patients. For them, we research, develop and manufacture innovative therapies for serious diseases, using living resources. This approach is based on cutting-edge technologies, such as human genetics, which enable us to characterise the molecular mechanisms at the root of diseases. Amgen focuses its research on diseases for which there is still a significant medical need.
With 18 drugs and numerous partnership initiatives, Amgen is working to advance the treatment of cancer, cardiovascular, inflammatory and renal diseases, as well as osteoporosis. With 54 active studies involving 964 patients in 294 centres (2022 figures), France is also one of the countries where Amgen has the largest clinical research activity.
Committed to research and to patients, Amgen is just as committed to its employees
Because we believe in a world where everyone can be themselves and play a role, Amgen France is socially committed through its Corporate Social Responsibility programme ) . In 2021, Amgen signed its first LGBT+ charter ) and the following year was awarded the "Very High Health, Social and Environmental Quality ) " label, making Amgen France the first pharmaceutical company to be awarded this label. We are also proud to have recently signed the Cancer and Employment charter to help our employees affected by the disease to remain in work and return to work.
What will tomorrow's healthcare be made of? Follow our news on , X (Twitter) @AmgenFrance, LinkedIn and Instagram. #LivingInnovating #WeAreBiotech
CLINICAL TRIAL MANAGER
LIVE
What you will do
Let's do this. Let's change the world. In this vital role you will be the primary point of contact to lead, manage and co-ordinate the conduct of clinical trials from study start-up to close out (CSR/Archival) at a country level in accordance with ICH-GCP and other applicable local regulations. You will maintain the quality and scientific integrity of clinical trials at a local/country level and actively collaborate with cross functional internal and external partners to ensure timely delivery, budget execution of clinical trial results within the local country.
Key Activities:
- Partner with global and local country teams to provide high level country strategy and actively drive study progress and local/country level study delivery
- Planning, management and oversight of clinical study execution in accordance with the global program strategy, through leadership with engagement of the cross-functional Local Study Team
- Communicate country status (including timelines and deliverables) to key partners including updates to relevant systems for transparency
- Provides country level input into the Country Operational Plan and partners with the Development Feasibility Manager through feasibility and with the Global Clinical Managers to ensure local delivery of the study
- Support internal audit and inspection activities and contribute to CAPAs, including leading resolution of issues when appropriate e.g., vendor management
- Assign and lead all aspects of deliverables of study support staff and continually review country level risk mitigation to ensure study delivers to plan
WIN
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The qualified professional we seek is a Trial Manager with these qualifications.
Minimum Requirements
- Doctorate degree OR
- Master's degree & 3 years of directly related experience OR
- Bachelor's degree & 5 years of directly related experience OR
- Associate's degree & 10 years of directly related experience OR
- High school diploma / GED & 12 years of directly related experience
- Advanced knowledge of global clinical trial management
- Fluency in local language and business English
Preferred Requirements
- BA/BS/BSc
- Minimum 2-3 years' experience of leading local/regional or global teams
- Minimum 2-3 years' clinical trial project management experience
- 7 years' work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
- Experience in management and oversight of external vendors (e.g., CROs, central labs, imaging vendors, etc.)
- Must be a local/country expert with proven project management experience locally
- Must be able to build strong site relationships as well as other local relationships to ensure end to end study delivery is met.
THRIVE
Some of the vast rewards of working here
As we work to develop treatments that take care of others, we also work to care for our teammates' professional and personal growth and well-being.
- Full support and career-development resources to expand your skills, enhance your expertise, and maximize your potential along your career journey
- A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
- Generous Total Rewards Plan—comprising health, finance and wealth, work/life balance, and career benefits—with compensation and benefits rated above 4 stars (out of 5) on Glassdoor
APPLY NOW
Join us in our mission to serve patients.
Amgen is committed to equal treatment, diversity and the inclusion of employees with disabilities, and is open to all. If you have a disability, do not hesitate to inform your Human Resources contact of any adaptations or tools required for the recruitment process to run smoothly. If you have any specific questions relating to your disability, please do not hesitate to ask them in confidentiality.
