Experienced Clinical Research Associates, Spain

hace 3 semanas


En remoto, España IQVIA A tiempo completo

**Join us in our exciting journey**:
**We are currently looking for dedicated Clinical Research Associates based in Madrid/Barcelona to join our Clinical Site Management team in IQVIA.**:
Whether you would like to broaden your therapeutic, geographic or study exposure, or you are looking a future beyond monitoring with our development opportunities, in IQVIA you will have training and development to plan and progress your career in the direction you choose, as we do not believe in a ‘career ceiling.’

The Clinical Site Management team works with multiple sponsors across a multitude of therapy areas and phases, giving you the opportunity to improve and develop your experience. With strategic site relationship managers supporting you throughout your role, this is a fantastic opportunity for you to embed yourself in the wider clinical operations team and work on ground-breaking new medicine development. Our clients are pharmaceutical companies who are dedicated and passionate about improving the lives of patients across several therapeutic areas.

Tasks and 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.

If appropriate, co-monitoring, training and mentoring of junior members in the team.

**Requirements**:
Bachelor's degree in a health care or other scientific discipline or educational equivalent.

At least 3 years of independent on-site monitoring experience.

Strong written and verbal communication skills including good command of English and Spanish.

In depth therapeutic and protocol knowledge as provided in company training.

What we offer

Genuine career development opportunities for those who want to grow as part of the organisation.

The chance to work on cutting edge medicines right at the forefront of new medicines development.

IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development

As a CRA you will receive an iPad and use of key developments such as site visit app’s, site visit report app’s that allow CRA’s to do their day job more efficiently.

Flexible conditions and an attractive remuneration package.

Location flexibility**:you can work either from our Madrid or Barcelona office or remotely from home.

LI-ELENALOP #LI-remote



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