In-house Cra, Multi-sponsor Team
il y a 1 semaine
Join us as we speed the delivery of ground-breaking therapies and anticipate tomorrow's drug development challenges, creating new possibilities for our clients and your career.
We are searching for an** **In-House CRA** to join our **multi-sponsor** team in **France**. This is a** **full-time** and **permanent position**.
As an essential member of the Project Team, the IHCRAs are responsible for supporting the execution of clinical trials. IHCRAs work closely with their CRA colleagues to maintain quality and deliver study milestones.
**Responsibilities include but are not limited to**:
- Monitoring site performance and creating action plans for sites not meeting expectations, in conjunction with the on-site CRA
- Assist CRAs with the preparation for site visits (running reports, QC of files, resolving action items from previous visits)
- Liaise with the project team and others to distribute and track clinical trial supplies to ensure sites have enough to continue recruitment
- Perform Case Report Form review, query generation and resolution, assisting sites as needed
- Document review and collection to ensure compliance and inspection readiness of TMF
- Tracking and processing invoices from investigator sites against agreed contracts and budgets
- Undertake project related administrative tasks (meeting minutes, recruitment tracking, site document preparation)
- IHCRA may also be required to attend onsite monitoring visits as a co-monitor with experienced CRAs to assist with tasks such as site regulatory file review and drug accountability
**Education and Qualifications**:
- University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
- Research experience in pharmaceutical or CRO industries may be considered
- Good organizational and time management skills
- Good communication skills
- Existing experience as a CTA/IHCRA or Site Coordinator preferred
- Fluency in French and English
**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.
For more information about how we collect and store your personal data, please see our Privacy Statement.
**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
-
Unblinded Cra
il y a 7 jours
Rueil-Malmaison, France Fortrea Temps pleinAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
Ctc Sponsor Dedicated
il y a 7 jours
Rueil-Malmaison, France Fortrea Temps plein**Job Overview**: The Senior Clinical Trial Administrator (Sr. CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the Sr. CTA shall reflect their experience, and level of contribution which they can make to the project. The CTA performs study-related tasks...
-
Senior Clinical Team Lead, Emea, Remote
il y a 2 jours
Rueil-Malmaison, France Labcorp Temps plein**Helping our clients make their clinical trials a success by orchestrating the efforts of top-talented Clinical Research Teams.** This is what our Senior Clinical Team Leaders live for: to drive the performance of clinical teams to achieve the highest project delivery, the best patient engagement and site management from a quality, timeline, budget and...
-
International Cra- Sites in France, Spain and
il y a 6 jours
Rueil-Malmaison, France Labcorp Temps plein4 to 5 Clear and confident health care decisions begin with questions. At Labcorp, we’re constantly in pursuit of answers. With unparalleled diagnostics and drug development capabilities, we accelerate innovation and provide insight to improve health and improve lives. Whether you’re a patient, provider, researcher or in the pharmaceutical industry,...
-
FSP Start Up Country Lead based in Paris region in France
il y a 4 jours
Rueil-Malmaison, Île-de-France Fortrea Temps pleinAre you passionate about clinical research and regulatory excellence? Fortrea is seeking a Start Up Country Lead to join our team in France. This role offers a unique opportunity to lead regulatory operations for clinical trials, ensuring compliance, quality, and timely delivery of study milestones in a dynamic and global environment.This is a...
-
Global Study Manager
il y a 14 heures
Rueil-Malmaison, France Labcorp Temps pleinIf you are looking for a company where you can personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view, consider working at Labcorp as a **Global Study Manager **for our Diagnostic Development Services department. In this role, you will be responsible for the successful delivery of the study...
-
Clin Res Assoc I
il y a 2 semaines
Rueil-Malmaison, Île-de-France Fortrea Temps pleinJob Overview:Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned.Summary of Responsibilities:Responsible for all aspects of study site monitoring including routine monitoring and closeout...
-
Site Start-Up Specialist based in France
il y a 7 jours
Rueil-Malmaison, Île-de-France Fortrea Temps pleinJoin Our Team and Drive Clinical Research SuccessAt Fortrea, we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist, you will play a pivotal role in coordinating site start-up activities, managing essential documents, and ensuring regulatory submissions are completed efficiently. Your expertise will...
-
Senior Field Clinical Research Associate
il y a 2 jours
Rueil-Malmaison, France Seagen Temps pleinPosition Summary: The Sr. Field CRA is responsible for monitoring and management of clinical sites. This position focuses on all activities required to evaluate, initiate, monitor and close clinical sites in compliance with the Code of Federal Regulations and ICH/GCP Guidelines. The Sr. Field CRA may act as mentor for junior members of the Field CRA team....
-
Sr Clinical Research Associate I
il y a 4 jours
Rueil-Malmaison, Île-de-France Fortrea Temps pleinJob Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans, as assigned. Function as leader for projects of limited scope, as assigned....