Experienced Clinical Research Associate, Multi-Sponsor, France
il y a 2 semaines
Experienced Clinical Research Associate, Multi‑Sponsor, France Engage in a structured training program to gain the knowledge and skills required to independently conduct clinical monitoring visits in accordance with the study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements. Essential Functions Complete appropriate therapeutic, protocol and clinical research training to perform job duties. Gain experience in study procedures by working with experienced clinical staff. Under close supervision, perform site monitoring visits (selection, initiation, monitoring and close‑out visits) in accordance with contracted scope of work and good clinical practices. Under close supervision, administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Under close supervision, 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. Under close supervision, ensure copies/originals (as required) of site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with Good Clinical Practice (GCP), International Conference on Harmonisation (ICH) and local regulatory requirements. Under close supervision, may support start‑up phase. Under close supervision, 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, learn key facets for successful development of a project subject recruitment plan on a per‑site basis. Suggest ideas for improving site recruitment plan in line with project needs to enhance predictability. Assist in tracking subject site recruitment progress. Qualifications Bachelor's Degree in a scientific discipline or health care preferred. Equivalent combination of education, training and experience may be accepted in lieu of degree. Prior clinical experience preferred. Some organizations may require 2 years of clinical experience. Computer skills including proficiency in Microsoft Word, Excel and PowerPoint and use of a laptop and mobile devices (iPhone/iPad) where applicable. Written and verbal communication skills with good command of the 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. Advanced knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines. Knowledge of applicable protocol requirements as provided in company training. Location: Paris, Lille, Lyon, Marseille, Bordeaux #J-18808-Ljbffr
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Clinical Research Associate, Multi‑Sponsor
il y a 2 semaines
Courbevoie, France IQVIA Temps pleinA leading clinical research organization is seeking an Experienced Clinical Research Associate to conduct monitoring visits and ensure compliance with study protocols and regulations. The ideal candidate will have a Bachelor's degree in a scientific field or health care, and some clinical experience is preferred. This role includes responsibilities such as...
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Clinical Research Associate 2, Sponsor-dedicated
il y a 4 jours
Courbevoie, Île-de-France IQVIA Temps pleinIQVIA Clinical Functional Services Partnerships (FSP) business is unique. Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our customers. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study.Leadership recognizes the skills, talent and experience of...
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Experienced Clinical Trials Assistant
il y a 4 jours
Courbevoie, France IQVIA Temps plein**Job Overview** Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining...
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Clinical Research Associate 2
il y a 4 jours
Courbevoie, France IQVIA Temps pleinThe IQVIA Research and Development Solutions team is focused on helping our healthcare customers to find innovative treatments solutions for patients with the common, large or rarest illnesses. As a CRA for Site Management department, you may work across different therapeutic areas following our internal SOPs. We seek dynamic and motivated people who truly...
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Junior Clinical Research Associate
il y a 4 jours
Courbevoie, France IQVIA Temps pleinJob Overview Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements. Essential Functions - Complete appropriate therapeutic, protocol and clinical research...
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Clinical Research Associate
il y a 4 jours
Courbevoie, Île-de-France IQVIA Temps pleinDue to our continued growth, we are recruiting for a Sr. Clinical Research Associates to join our team. This 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...
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Experienced Clinical Trials Assistant
il y a 1 jour
Courbevoie, France IQVIA Temps pleinThe IQVIA Research and Development Solutions team is focused on helping our healthcare customers to find innovative treatments solutions for patients with the common, large or rarest illnesses. Providing administrative support to the clinical teams members could make your contribution to the research. We seek dynamic and motivated people who truly want to...
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Associate Clinical Project Manager, Sponsor-dedicated, Paris Based
il y a 1 semaine
Courbevoie, France IQVIA Temps pleinAssociate Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Associate Project Lead is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies...
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Clinical Trials Assistant
il y a 6 jours
Courbevoie, Île-de-France IQVIA Temps pleinCourbevoie, France | Full time | Hybrid | R1523568Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential FunctionsAssist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with...
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Clinical Trials Assistant
il y a 4 jours
Courbevoie, Île-de-France IQVIA Temps pleinThe IQVIA Research and Development Solutions team is focused on helping our healthcare customers to find innovative treatments solutions for patients with the common, large or rarest illnesses. Providing administrative support to the clinical teams members could make your contribution to the research. We seek dynamic and motivated people who truly want to...
