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...

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...

Discover a new career opportunity with IQVIA as a clinical research manager for a sponsor-dedicated team.At IQVIA, we offer a unique approach to clinical research, with dedicated teams working closely with a single sponsor partner to deliver high-quality results. Our clinical research associates (CRAs) are 'indication and molecule experts', contributing to...

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. 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...

OverviewThe Clinical Trials Assistant will provide administrative support to the clinical research team at Pharmiweb. This role is a key part of our team and will help us deliver high-quality clinical research services to our clients.Key ResponsibilitiesSupport the clinical research team with administrative tasks, including data entry, filing, and...

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. 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...

**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...

Strengthen our self-care medical device division by joining our team as 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 self-care medical...

**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...

IQVIA, with more than 75,000 employees worldwide, is a leader in information, innovative technologies and clinical research services in the healthcare sector. Resulting from the merger between IMS Health and Quintiles, IQVIA combines analytical rigor, data precision and new technologies to meet the challenges of changes in the world of health. This...

**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...

**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...

**Company Description** Mazars is an internationally integrated partnership, specialising in audit, accountancy, advisory, tax and legal services*. Operating in over 100 countries and territories around the world, we draw on the expertise of more than 50,000 professionals - 33,000+ in Mazars’ integrated partnership and 17,000+ via the Mazars North America...

**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,...

Provide 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,...

**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...

**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...

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

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).Responsibilities:Prepare and...