Senior CRA - Multisponsor
IQVIA
Oeiras, Portugal
há 4 dias
source : Pharmiweb
  • Join us in our exciting journey!!*We currently require a motivated, passionate and enthusiastic clinical trials professional to join our rapidly growing *Site Management* division.
  • As an experienced *Senior Clinical Research Associate*, you could be looking to broaden your therapeutic, geographic or study exposure.

  • Or perhaps you are looking for 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.’This role is working in our core clinical site management function. The 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.

  • The role : Responsibilities*Perform site selection, initiation, monitoring and close-out visits and work with sites to adapt, drive and track subject recruitment plans.
  • 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*Our ideal candidate : Skills & other requirements*In depth knowledge and skill in applying applicable clinical research regulatory requirements, i.

    e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesIn depth therapeutic and protocol knowledge as provided in company trainingExcellent organizational and problem-solving skillsEffective time management skillsStrong written and verbal communication skills including good command of English and Portuguese.

    Bachelor's degree in a health care or other scientific discipline or educational equivalentMínimum 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 (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.

    IQVIA™ is an equal opportunity employer. We make employment decisions based on qualifications and merit. We prohibit discrimination based on any unlawful consideration such as age, race, national origin, gender or other "protected status.

    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!*Are you interested or do you know the ideal candidate?

  • If you know the right candidate or for more information on this role, please contact *patricia.ramos iqvia.com Please note is necessary that your application is registered in our Talent Network to process your candidacy*IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
  • We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world.

    Learn more at https : / / jobs.iqvia.com (https : / / jobs.iqvia.com / )

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