Clinical Research Associate Internship

The 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...

The IQVIA Internship provides you with the opportunity to gain relevant, project-based work experience at one of the most successful and cutting-edge global clinical research units in the market while building relationships within the company that will impact your future. You will be working in our **Clinical Research Associate Team** together with some of...

The 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. The Global Site Activation team will help them to decrease the site activation time and help the site to be ready to recruit patients faster. We seek dynamic and...

**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...

**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...

**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...

To strengthen our self-care medical device division, RNI – a PLG company, is seeking a Scientific Affairs Associate for Medical Devices with experience in evaluating the efficacy and safety of health products in the European market. In this role, you’ll work closely with Senior Consultants in a small dynamic team, overseeing the entire life cycle of...

**Location**:Courbevoie, FR, 92400**Function**:Legal**Employment type**:Full Time**Required experience**:Student**Reference ID**:74669Internship - Public Affairs **ONBOARDING YOU TO THE COMPANY** - At Nexans our global vision is to electrify the future. At Nexans' Innovation Business Group this means innovation beyond cable to bring differentiation and...

**Job Family**:EMEA Strategy Consulting **Location**:[Paris/Munich/Madrid/Basel/Amsterdam] **Real World Commercial Solutions to Create a Healthier World** In RWCS we’re passionate about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world. Every day our team develops evidence-based strategies that...

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. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...

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. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted...

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. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...

**We are growing, grow with us!** Are you looking for a dynamic company with daily new challenges and opportunities? Then, Pharmalex is your career opportunity. Pharmalex is one of the leading service companies for the Pharmaceutical Industry globally and is specialized in all aspects of drugs and medical devices approval, of the market development and any...

Your Job Management of patient inclusions in accordance with AAP/AAC and client requirements Management of patient follow-up forms: information verifications, clarifications, requests’ approval or refusal, data recording Full management of purchase order forms from hospitals and pharmacists Management of calls and emails with healthcare...

**À propos de nous** Points clés de notre environnement de travail: - Bureaux modernes - Repas fourni - Journées de télétravail - Opportunités d'évolution Job Responsibilities : You will be joining a multidisciplinary expert team supervised by the Research & Innovation Director, in collaboration with Business Unit Product development Director and...

**Lieu**:Courbevoie, FR, 92400**Fonction**:Juridique**Type d'emploi**:Temps plein**Expérience requise**:Etudiant**N° de l'offre**:74669STAGIAIRE - Affaires Publiques, compliance **VOUS INTÉGRER DANS L'ENTREPRISE** - Chez Nexans, notre vision globale est d'électrifier le futur. Au sein du Groupe, cela signifie innover au-delà du câble pour apporter...

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. - Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted...

We are seeking a highly motivated and detail-oriented Regulatory Affairs specialist to join our pharmaceutical company. The Regulatory Affairs Specialist will be responsible for ensuring compliance with regulatory requirements for the development, approval, and marketing of pharmaceutical products globally (internationally). Group 10...

Join us in healthcare innovation. For everyone. Wherever they are. Sustainably. Our inspiring and supportive environment creates a global community that celebrates diversity and individuality. We encourage you to step out of your comfort zone, offering resources and flexibility to enhance your professional and personal growth, while valuing your unique...

Your role   You will become the responsible for the management of regulatory affairs proposes by proposing, implementing and ensuring the implementation of a technical-regulatory strategy for the company in order to guarantee compliance with pharmaceutical regulations for the development, registration, and operation of products. As a regulatory...