Emplois actuels liés à Junior Clinical Research Associate - Lyon - Medpace

  • Entry Level

    il y a 2 semaines


    Lyon, France Medpace, Inc. Temps plein

    Job Summary: The Clinical Research Associate at Medpace is offering the unique opportunity to have an **exciting career** in the research of drug and medical device development. For those with **medical and/or health/life science interest and background** who want to explore the research field, **travel throughout France**, and be part of a team bringing...


  • Lyon, Auvergne-Rhône-Alpes, France Medpace Temps plein

    Medpace is currently seeking candidates with *Cardiovascular related Ph Ds and/or Post-Doctoral Research experience* for a full-time, office-based Associate Clinical Trial Manager (a CTM) to join our France, Lyon Clinical Trial Management team. The a CTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial...


  • Lyon, Auvergne-Rhône-Alpes, France Medpace Temps plein

    Medpace is currently seeking candidates with Gastrointestinal area *related PhDs and/or Post-Doctoral Research experience* for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our France, Lyon Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical...


  • Lyon, Auvergne-Rhône-Alpes, France Medpace Temps plein

    Medpace is currently seeking candidates with Radiopharmaceutical* related PhDs and/or Post-Doctoral Research experience* for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our France, Lyon Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical...


  • Lyon, Auvergne-Rhône-Alpes, France Medpace Temps plein

    Medpace is currently seeking candidates with *Cardiovascular related PhDs and/or Post-Doctoral Research experience* for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our France, Lyon Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial...


  • Lyon, Auvergne-Rhône-Alpes, France Medpace Temps plein

    Medpace is currently seeking candidates with Renal *related PhDs and/or Post-Doctoral Research experience* for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our France, Lyon Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in...


  • Lyon, France Icon plc Temps plein

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...


  • Lyon 7e, France AUROBAC THERAPEUTICS Temps plein

    **Presentation of the company**: AUROBAC THERAPEUTICS is a biopharmaceutical company created in 2022 by 3 renowned life sciences innovation companies, Boehringer Ingelheim, Evotec and bioMérieux, to become a global leader in the fight against bacterial infections, Antimicrobial Resistance (AMR) and their consequences in acute hospital settings such as...

  • Clinical Trial Manager

    il y a 2 semaines


    Lyon, France Medpace Temps plein

    Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Lyon, France. Clinical Trial Managers with expertise in Nephrology are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. We provide remote...

  • Clinical Study Manager

    il y a 7 jours


    Lyon, Auvergne-Rhône-Alpes, France Valneva Temps plein

    We are a specialty vaccine company that develops, manufactures, and commercializes prophylactic vaccines for infectious diseases addressing unmet medical needs.We have leveraged our expertise and capabilities both to commercialize three vaccines, including the world's first and only chikungunya vaccine, and to rapidly advance a broad range of vaccine...


  • Lyon, France Medpace Temps plein

    **Responsibilities **- Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager - Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy - Compile and maintain project-specific status reports within the clinical trial management system - Interact with the...


  • Lyon, France Icon plc Temps plein

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...

  • Study Start Up Associate Ii

    il y a 2 semaines


    Lyon, France ICON plc Temps plein

    Study Start Up Associate II At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation:...

  • Cra Ii

    il y a 6 jours


    Lyon, France KCR Temps plein

    **We see human behind every number** **Clinical Research Associate II** **Location**: Paris/Ile de France or Lyon (home based)** On behalf of our partner, one of the global leaders in clinical research, we are currently recruiting for a Clinical Research Associate II in France (Paris or Lyon). **As an experienced Clinical Research Associate** you will be...

  • Medical Director

    il y a 3 semaines


    Lyon, Auvergne-Rhône-Alpes, France Medpace Temps plein

    We are seeking a Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the...

  • Clinical Trial Assistant

    il y a 5 jours


    Lyon, France Medpace, Inc. Temps plein

    Job Summary: Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Trial Assistant to join our Clinical Trial Management team in Lyon. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your...


  • Lyon, France bioMérieux sa Temps plein

    A family-owned company, bioMérieux has grown to become **a world leader in the field of in vitro diagnostics**. For 60 years and across the world, we have imagined and developed **innovative diagnostics solutions** to **improve public health**. Today, our teams are spread across 45 countries and serve 160 countries with the support of a large distribution...

  • Clinical Veterinarian

    il y a 3 semaines


    Lyon, Auvergne-Rhône-Alpes, France Eslav Temps plein

    Company name: Charles River Laboratories Safety AssessmentCity: LyonCountry: FranceAs a clinical veterinarian, you work within a team of 3 veterinarians and a veterinarian manager within a strict regulatory framework (GLP and regulation applicable to laboratory animals) and ensure the clinical, medical and health monitoring of all the animals in the company...

  • Clinical Trials Assistant

    il y a 2 semaines


    Lyon, France Bespoke Recruitment Temps plein

    **Clinical Trials Assistant for a multinational pharmaceutical company in CORK, IRELAND.** **Funded relocation package: é2000 + 2 weeks paid accommodation** **PRIMARY RESPONSABILITIES** Clinical Trial Responsibilities - Initiate investigator site activities, including collection and submission of regulatory documents. - Track and ensure site compliance...

  • Market Research Manager

    il y a 2 semaines


    Lyon, France bioMérieux Temps plein

    **Market Research Manager - All Genders**: Location: Marcy l'Etoile, France Position Type: Unfixed Term Job Function: Clinical Affairs A family-owned company, bioMérieux has grown to become **a world leader in the field of in vitro diagnostics**. For 60 years and across the world, we have imagined and developed **innovative diagnostics solutions** to...

Junior Clinical Research Associate

il y a 3 semaines


Lyon, France Medpace Temps plein

The Clinical Research Associate - L'attaché(e) de recherche clinique position at Medpace offers the unique opportunity to have an **exciting career** in the research of drug and medical device development while **making a difference** in the lives of those around them. For those with a **medical and/or health/life science background** who want to explore the research field, **travel in France**, and be part of a team bringing pharmaceutical and medical devices to market - **this could be the right opportunity for you**

Our successful Clinical Research Associates possess various backgrounds in medical and other science-related healthcare fields. Backgrounds of individuals who have succeeded in the CRA role include:
**MEDPACE CRA TRAINING PROGRAM PACE® (Professionals Achieving CRA Excellence).**

No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our **PACE®**Training Program, you will join other **P**rofessionals **A**chieving **C**RA **E**xcellence:

- **PACE®**provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.
- **PACE®**will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums.
- To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.

**WHY BECOME A CRA**

This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:

- Dynamic working environment, with varying responsibilities day-to-day
- Expansive experience in multiple therapeutic areas
- Work within a team of therapeutic and regulatory experts
- Defined CRA promotion and growth ladder with potential for mentoring and management advancementsCompetitive pay and m any additional perks unmatched by other CROs (SEE BELOW).

**UNEXPECTED REWARDS**

This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:

- Mid-sized CRO where you are not just a number
- Dynamic working environment, with varying responsibilities day-to day
- Expansive experience in multiple therapeutic areas
- Work within a team of therapeutic, medical and regulatory experts
- Internally designed propriety Clinical Trial Management System - one stop shop for EDC, IWRS, regulatory portal, visits reports, and more
- Defined CRA promotion and growth ladder with potential for mentoring and management advancements
- Opportunity to work from home once job experience is gained
- Competitive pay.

**Responsibilities**
- Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
- Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;
- Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
- Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements;
- Regulatory document review;
- Medical device and/or investigational product/drug accountability and inventory;
- Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
- Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and
- Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

**Qualifications**
- Bac+5 in Pharmacy or a health or science related field;
- Ability to travel 60-80% to locations nationwide is required;
- Must maintain a valid driver’s license and the ability to drive to monitoring sites;
- Minimum 1 year healthcare-related work experience preferred;
- Fluent in **French** & **English** is a must;
- Strong communication and presentation skills; andMust be detail-oriented and efficient in time management.

**Medpace Overview**

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical develo