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Emplois Icf (95224 Herblay)

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    • IQVIA’s Global Site Activation Teamof 2000 employees,drivesbest inclasssite and customer experience,withindustry leadingoutcomes.
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    • Paris, France | Full time | Home-based | R1546701.
    • PTA here refers to the provision of investigational product for the intent of treatment, in a non-trial…
    • Manage the end-to-end clinical site contracting process (drafting, negotiation, amendments, termination, signature collection and archiving).

Job Post Details

Country Site Activation Internship - 6 months - job post

IQVIA
3.7/5 étoiles
Courbevoie (92)
Temps plein
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Détails de l'emploi

Type de poste

  • Temps plein

Lieu

Courbevoie (92)

Description du poste

Courbevoie, France | Full time | Hybrid | R1546279


Make an impact on patient health!

IQVIA’s Global Site Activation Teamof 2000 employees,drivesbest inclasssite and customer experience,withindustry leadingoutcomes.

We keep the patient at the forefront; ‘Always Impatient for the Patient’and we excel in our collaboration with our external/internal customers.

IQVIA’s Country Site Activation teamare aglobal network whoidentifyandactivate sites to thehighestquality toensure patients on Clinical trials have access to safe and effective medication.

We are leaders in innovation and first tonew technologies,meaning a vast amount of career development opportunities are available.

Job Overview
Under supervision, executes the site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at country level.

Job Responsbilities

  • With supervision, serve a Single Point of Contact (SPOC) to perform site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.

  • Prepare site documents, reviewing for completeness and accuracy.

  • Inform team members of completion of regulatory contractual. and other documents for individual sites.

  • Distribute completed documents to sites and internal project team members.

  • Update and maintain internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.

  • Review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.



Qualifications

  • Bachelor's Degree Life sciences or a related field. Desirable specific training in clinical research or CRA school.

  • Desirable 1 - 3 years’ clinical research or other relevant experience; or equivalent combination of education, training and experience.

Join IQVIA andlet’screate a healthier world together:

  • Exposure across21Therapeutic Areas

  • Be part of aglobal team whooperateacross 141 locations

  • Exposure acrossa variety of studies and projects

  • Access tonew, innovativetechnologies

  • Work within a collaborative and vibrant environment

  • Own your career!

Unleash your potential!

It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world.

When you join our diverse, global team,you’llharness the power of unparalleled data, advanced analytics,cutting-edgetechnologies, and deep healthcare and scientificexpertiseto drive healthcare forward.

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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