Clinical Research Associate - IQVIA BIOTECH (homebased in France) job opportunity at IQVIA Holdings, Inc..

Home Jobs In France Tag: Job Clinical Research Associate - IQVIA BIOTECH (homebased in France) position at IQVIA Holdings, Inc.


bot
IQVIA Holdings, Inc. Clinical Research Associate - IQVIA BIOTECH (homebased in France)
Experience: 1-years
Pattern: full-time
Country:
apply Apply Now
Salary:
Status:

Job

Copy Link Report
degreeAssociate
loacation Paris, France, France
loacation Paris, France....France

Due to our continued growth, we are recruiting for a Sr. Clinical Research Associates to join our team. T his is a great opportunity for a CRA to join a progressive and developing CRO. IQVIA Biotech is unique division specialising in working with smaller biotech and emerging biopharma clients, and as such we have a vibrant, fast-paced working environment.   Responsibilities • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. • Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. • Collaborate and liaise with study team members for project execution support as appropriate. • If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. • If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications Background within either Life Science, Nursing, Pharmacy or a medical degree • Previous experience as a Study Coordinator  • Minimum of 1 year of experience in Monitoring on Site visits one or more therapy areas, ideally oncology • Bachelor's Degree Degree in scientific discipline or health care preferred. Req • Equivalent combination of education, training and experience may be accepted in lieu of degree. • Some organizations require completion of CRA training program or prior monitoring experience. • Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). • Good therapeutic and protocol knowledge as provided in company training. • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). • Written and verbal communication skills including good command of English language. • Organizational and problem-solving skills. • Effective time and financial management skills. • Ability to establish and maintain effective working relationships with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com

Other Ai Matches

Freelance- Translators/Linguists, English into Portugese (Brazil) Applicants are expected to have a solid experience in handling English into Portugese (Brazil) related tasks
Receptionist Applicants are expected to have a solid experience in handling Job related tasks
Account Sales Applicants are expected to have a solid experience in handling Job related tasks
Internal Medical Translator - English to Japanese Applicants are expected to have a solid experience in handling Job related tasks
Digital Account Manager 2 (Remote) / Gestionnaire de comptes numériques 2 (à distance) Applicants are expected to have a solid experience in handling Job related tasks
Contact Center Analyst - German Speaking Applicants are expected to have a solid experience in handling Job related tasks
Regulatory Operations Coordinator Applicants are expected to have a solid experience in handling Job related tasks
Inventory Control Associate (6 months Temp) Applicants are expected to have a solid experience in handling Job related tasks
Clinical Research Associate - Sponsor Dedicated Applicants are expected to have a solid experience in handling Job related tasks
MedTech Field Service Technician - On-Call / Per Diem - Eugene/Portland, OR Applicants are expected to have a solid experience in handling OR related tasks
Consultant, Management Consulting Applicants are expected to have a solid experience in handling Management Consulting related tasks
Clinical Research Associate, IQVIA Biotech Applicants are expected to have a solid experience in handling IQVIA Biotech related tasks
Clinical Specialist / Stroke Rater - Chinese Speaking Applicants are expected to have a solid experience in handling Job related tasks
MedTech Part Time Clinical Consultant – Fort Worth, TX Applicants are expected to have a solid experience in handling TX related tasks
SAP Business SD Analyst Applicants are expected to have a solid experience in handling Job related tasks
Pharmaceutical Sales Representative - Urology - Phoenix, AZ Applicants are expected to have a solid experience in handling AZ related tasks
MedTech Field Service Technician - PM - Baltimore MD / Richmond VA Applicants are expected to have a solid experience in handling Job related tasks
Délégué(e) Hospitalier Biosimilaires - Bretagne/ Pays de la Loire F/H Applicants are expected to have a solid experience in handling Job related tasks
Project Finance Asst 1 Applicants are expected to have a solid experience in handling Job related tasks
Pharmaberater m/w/d Orphan Drugs, HKL/Kardiologie Applicants are expected to have a solid experience in handling HKL/Kardiologie related tasks
Flex Nurse Educator - Spokane, WA (Must have/obtain CA license) Applicants are expected to have a solid experience in handling WA (Must have/obtain CA license) related tasks
Product Owner, Health Data & Tokenization Applicants are expected to have a solid experience in handling Health Data & Tokenization related tasks
Pharmaberater m/w/d Diabetes HKL Kardiologie Applicants are expected to have a solid experience in handling Job related tasks