Junior Clinical Research Associate
Il y a 4 mois
Job 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 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 establishes 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) 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 Harmonization (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.
Qualifications
- 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.
- Prior clinical experience preferred.
- Some organizations may require 2 years of clinical experience.
- 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.
- Advanced knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Knowledge of applicable protocol requirements as provided in company training.
-
Clinical Research Associate Internship
Il y a 7 mois
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. You would like to be engaged in the company training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance...
-
Clinical Research Associate Internship
Il y a 2 mois
Courbevoie, France IQVIA Temps plein**CRA Internship - Office Based Paris** **IQVIA Offers fantastic opportunity for Graduates and Professionals who wish to become a CRA.** By joining IQVIA as CRA Intern you will engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating...
-
Clinical Research Associate
il y a 3 semaines
Courbevoie, France Pharmiweb 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 environment....
-
Clinical Trials Assistant
Il y a 4 mois
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...
-
Clinical Research Associate 2
Il y a 4 mois
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...
-
Global Analyst, Clinical Trail Analytics and
il y a 4 semaines
Courbevoie, France IQVIA Temps pleinWe are seeking Global Analyst to join our innovative department, Clinical Trail Analytics and Strategic Insights (CTA&SI) that is a part of IQVIA's Applied Data Science Center. **Job Overview**: Global Analyst will be responsible for providing input into the generation of clinical study strategies and collaborating with other involved IQVIA teams to perform...
-
Clinical Trial Manager
Il y a 7 mois
Courbevoie, France IQVIA Temps plein**Clinical Trial Manager** Global or Regional Applicability: Regional Trial Management services provide local management of a clinical trial (s) (or Medical Affairs data generation activity) in a country or countries. Services/deliverables include operational oversight of assigned project(s) at the country level for end-to-end project management from...
-
Clinical Trials Coordinator- Based in Paris
Il y a 7 mois
Courbevoie, France IQVIA Temps plein**Join us in our exciting journey!** We currently require a motivated and enthusiastic clinical trials professional to join our rapidly growing international division as a Clinical Trials Coordinator. Our client is one of the TOP 5 pharmaceutical companies who is dedicated and passionate about improving the lives of patients across several therapeutic...
-
Clinical Trial Coordinator
Il y a 7 mois
Courbevoie, France IQVIA Temps plein**Join us in our exciting journey!**: We currently require a motivated and enthusiastic clinical trials professional to join our rapidly growing international division as a Clinical Trials Coordinator. Our client is one of the TOP 5 pharmaceutical companies who is dedicated and passionate about improving the lives of patients across several therapeutic...
-
Clinical Project Manager, Sponsor-dedicated, Paris based
il y a 3 semaines
Courbevoie, France Pharmiweb Temps pleinJob OverviewProject 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 Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs,...
-
Trusted Partners Associate
il y a 4 semaines
Courbevoie, France Potloc Temps pleinAs Potloc’s **Trusted Partners Associate** your role will be to assist in consolidating the company’s network of trusted partners (incl. marketplaces) into an industry-leading ecosystem based on reliability, data quality and speed.You will report to the Supply Partnership Manager and will actively participate in expanding, optimizing and automating...
-
Medical Science Liaison
Il y a 2 mois
Courbevoie, France IQVIA Temps plein**Medical Science Liaison - Oncology - France / Belgium** IQVIA is looking for an MSL (Medical Scientific Liaison) based in France to join our client’s global oncology team as they prepare for launch of a next generation TKI for kidney, metastatic colorectal and head & neck cancers. **_ Responsibilities:_** - Provide field-based medical support to the...
-
Trusted Partners Associate
il y a 3 semaines
Courbevoie, 92400, France Potloc Temps pleinAs Potloc’s **Trusted Partners Associate** your role will be to assist in consolidating the company’s network of trusted partners (incl. marketplaces) into an industry-leading ecosystem based on reliability, data quality and speed.You will report to the Supply Partnership Manager and will actively participate in expanding, optimizing and automating...
-
Trusted Partners Associate
il y a 3 semaines
Courbevoie, 92400, France Potloc Temps pleinAs Potloc’s **Trusted Partners Associate** your role will be to assist in consolidating the company’s network of trusted partners (incl. marketplaces) into an industry-leading ecosystem based on reliability, data quality and speed. You will report to the Supply Partnership Manager and will actively participate in expanding, optimizing and automating...
-
Senior Associate Renewable Energy
Il y a 4 mois
Courbevoie, France KPMG Temps pleinVos challengesVotre mission, en tant que Senior Associate Renewable Energy Advisory F/H consiste à : * Construire, réviser et tester les modèles financiers utilisés pour les mandats de fusions et acquisitions et de financement, ainsi que traduire l'analyse financière en recommandations concises des clients * Diriger une équipe d'analystes dans la...
-
Data Manager
Il y a 2 mois
Courbevoie, France IQVIA Temps plein**Missions**: - Writing the CRF - Drafting basic documentation: basic structure, DVP, DMP; DHR - eCRF and ePRO designing and testing - Programming of Data Review listings (SAS) - Edition of the Data Review report - Basic cleaning conventions programming - Quality control of the documentation and programs of junior data managers - Database lock and...
-
Executive Asssociate Renewables
il y a 3 jours
Courbevoie, France KPMG Temps pleinVous souhaitez évoluer dans un cabinet leader qui vous permet de vivre vos convictions? Comme nos 10 000 collaborateurs, faites le choix d’une société à mission en plein essor, où la contribution de chacun et chacune est encouragée pour grandir ensemble. Faites le choix d’exceller autrement en œuvrant pour une performance durable autant que...
-
Executive Associate Renewables
Il y a 7 mois
Courbevoie, France KPMG Temps pleinVous souhaitez évoluer dans un cabinet leader qui vous permet de vivre vos convictions? Comme nos 10 000 collaborateurs, faites le choix d’une société à mission en plein essor, où la contribution de chacun et chacune est encouragée pour grandir ensemble. Faites le choix d’exceller autrement en œuvrant pour une performance durable autant que...
-
Experienced Cra
Il y a 7 mois
Courbevoie, France IQVIA Temps plein**Job Overview** Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. This role requires fluency in the English language. **Essential Functions** - Perform site monitoring visits (selection,...
-
Fsp - Trial Manager - France
il y a 1 mois
Courbevoie, France IQVIA Temps pleinProvide global, regional or complex local management of a clinical trial (s) (or Medical Affairs data generation activity) in a country or countries. Services/deliverables include operational oversight of assigned project(s) at the country level for end-to[1]end project management including start-up, execution, close-out, analysis and reporting. Further,...