Clinical Research Associate

hace 7 días


En remoto, España IQVIA A tiempo completo

**Join us in our exciting journey**:
We currently require a motivated, passionate and enthusiastic clinical trials professional to join our rapidly growing **Clinical Functional Service Partnership** (CFSP) division.

As an experienced **Clinical Research Associate**, you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking a future beyond monitoring with our development opportunities. At IQVIA, you’ll have training and development to plan and progress your career in the direction you choose; we do not believe in a ‘career ceiling.’

IQVIA is expanding in Spain - we currently have multiple exciting vacancies for **Junior **Clinical Research Associates to work sponsor-dedicated** **to one of our key pharmaceutical clients**. If you have independent site monitoring experience as CRA and want to discover how a true partnership between the CRO and sponsor works, then this is the right opportunity for you

Our clients are pharmaceutical companies who are dedicated and passionate about improving the lives of patients across several therapeutic areas.

**The role: Responsibilities**
- Administer protocol and related study training to assigned sites and establish regular lines of communication.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations - escalating quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans
- In depth therapeutic and protocol knowledge as provided in company training
- Excellent organizational and problem-solving skills
- Effective time management skills
- Strong written and verbal communication skills including good command of English and Spanish
- ** Bachelor's degree in a health care or other scientific discipline or educational equivalent**:

- ** 1-3 years of independent on-site monitoring experience**

**What we offer**
- Working with one of the TOP 5 sponsors globally on international projects.
- Focus on quality, not quantity We invest in keeping our teams stable, so workload is consistent.
- The chance to work on cutting edge medicines right at the forefront of drug development.
- Genuine career development opportunities for those who want to grow as part of the organization.
- Flexible conditions and an attractive remuneration package.
- Office or home-based roles available

**We invite you to join IQVIA**
- Recognized by **Great Place to Work** as the second best company to work for in Spain (March 2019)
- ** FORTUNE Magazine's World's Most Admired Companies** list for the third year in a row (January 2020)
- Recognized by the 2016 Scrip Awards as the **Best Full-service Provider Contract Research Organization** (CRO)
- Awarded the 2016 Eagle Award from the Society for Clinical Research Sites (SCRS) for the fourth consecutive year.
- A site-nominated award recognizing contract research organizations (CRO) and biopharmaceutical sponsors dedicated to **building positive relationships with research sites through leadership, professionalism and integrity**.
- IQVIA named in The International Association of Outsourcing Professionals (IAOP) 2017 Global Outsourcing 100® List which recognizes the world’s best service providers across a range of industries.

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, **we invite you to reimagine healthcare with us**. You will have the opportunity to play an important part in helping our clients drive healthcare forward and whatever your career goals, we are here to ensure you get there



  • En remoto, España IQVIA A tiempo completo

    Join us in our exciting journey:We currently require a motivated, passionate and enthusiastic clinical trials professional to join our rapidly growing Clinical Functional Service Partnership (CFSP) division.As an experienced Clinical Research Associate, you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking...


  • En remoto, España Parexel A tiempo completo

    Everything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction. As a CRA...


  • En remoto, España ICON A tiempo completo

    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...


  • En remoto, España IQVIA A tiempo completo

    **Join us in our exciting journey!!**: We currently require a motivated, creative and enthusiastic clinical trials professional to join our rapidly growing Site Management division. As an experienced **Clinical Research Associate**, you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking a future beyond...


  • En remoto, España IQVIA A tiempo completo

    Join us in our exciting journey:We currently require a motivated, creative and enthusiastic clinical trials professional to join our rapidly growing Site Management division.As an experienced Clinical Research Associate, you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking a future beyond monitoring with...


  • En remoto, España Parexel A tiempo completo

    Everything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction. As a CRA...


  • En remoto, España ICON A tiempo completo

    You will be supporting a long-term partnership with one of the most established pharmaceutical companies in the industry. Within this program you will find a culture focused on teamwork and camaraderie; where every member plays an integral part. You will have the opportunity to work on breakthrough technologies in the areas of cardiovascular, oncology,...


  • En remoto, España IQVIA A tiempo completo

    Join us in our exciting journey:We currently require a motivated, creative and enthusiastic clinical trials professional to join our rapidly growing Site Management division.As an experienced Clinical Research Associate, you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking a future beyond monitoring with...


  • En remoto, España IQVIA A tiempo completo

    **Join us in our exciting journey!!**: We currently require a motivated, creative and enthusiastic clinical trials professional to join our rapidly growing Site Management division. As an experienced **Clinical Research Associate**, you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking a future beyond...


  • En remoto, España ICON A tiempo completo

    As a Senior Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: - You will monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas. Assist other CRAs with co-monitoring activities...


  • En remoto, España OPIS s.r.l. A tiempo completo

    Founded in 1998 in Italy and now operating at an international level, OPIS is a full-service science driven biotech focused CRO providing premium trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of current projects. OPIS added...


  • En remoto, España ICON A tiempo completo

    As a Senior Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing: You will monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas. Assist other CRAs with comonitoring activities both remote and...


  • En remoto, España Parexel A tiempo completo

    The **Initiation Clinical Research Associate II **(**iCRA II**) specialises in performing all study start up activities for a clinical trial. You will participate in Pre SIV activities and be assigned & accountable for managing and driving the strategy for the Pre SIV / start up tasks of the study. The iCRA II can also support protocol amendments if...


  • En remoto, España Allucent A tiempo completo

    These customers have new therapeutic ideas, but want a partner who can assist with the clinical trial process, the complexities of certain disease states, or other critical capacities. You’ll work with them on the newest treatment breakthroughs for some of the most perplexing conditions. And ultimately, you’ll help make a positive difference in...


  • En remoto, España Parexel A tiempo completo

    The **Initiation Clinical Research Associate (iCRA)** specialises in performing all study start up activities for a clinical trial. You will participate in Pre SIV activities and be assigned & accountable for managing and driving the strategy for the Pre SIV / start up tasks of the study. The iCRA I can also support protocol amendments if applicable. This...


  • En remoto, España ICON A tiempo completo

    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...


  • En remoto, España Parexel A tiempo completo

    Additional Job DescriptionThe Initiation Clinical Research Associate II (iCRA II) specialises in performing all study start up activities for a clinical trial. You will participate in Pre SIV activities and be assigned & accountable for managing and driving the strategy for the Pre SIV / start up tasks of the study. The iCRA II can also support protocol...


  • En remoto, España Allucent A tiempo completo

    These customers have new therapeutic ideas, but want a partner who can assist with the clinical trial process, the complexities of certain disease states, or other critical capacities. You'll work with them on the newest treatment breakthroughs for some of the most perplexing conditions. And ultimately, you'll help make a positive difference in patients'...


  • En remoto, España Parexel A tiempo completo

    The Initiation Clinical Research Associate (iCRA) specialises in performing all study start up activities for a clinical trial. You will participate in Pre SIV activities and be assigned & accountable for managing and driving the strategy for the Pre SIV / start up tasks of the study. The iCRA I can also support protocol amendments if applicable. This role...


  • En remoto, España Parexel A tiempo completo

    Everything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction.As a CRA at...