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Clinical Research Associate - Ireland

Location: Dublin, Ireland
R1212368

When you join IQVIA as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers. Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development.

With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.

  • Full Time
  • Level: Entry-level, Mid-level, Senior-level
  • Travel: Yes

Success profile

What makes sponsor-dedicated CRAs at IQVIA successful? Check out the top traits we’re looking for and see if you have the right mix.

  • COLLABORATIVE
  • DETAIL-ORIENTED
  • COMMUNICATOR
  • INDEPENDENT
  • CURIOUS
  • PROBLEM-SOLVER

Explore this
career path

As you grow your CRA career at IQVIA, you’ll play an important role in helping our customers drive healthcare forward and impact the lives of patients around the world.

Quote

Alberto

IQVIA offers a robust development plan for CRAs, including trainings, mentorship programs, and cross-functional career meetings. These conditions made me feel ready, confident and well-trained to execute the role of a CRA with quality and integrity.

Alberto, Clinical Research Associate 2
Oliver

IQVIA places real emphasis on the training and development of employees. This is invaluable for someone starting out or looking to progress their career in clinical research. I find it extremely rewarding to work for a company that strives to grow and retain its talent and equips you with the skills and experience needed to succeed in your career.

Oliver, Clinical Research Associate 1

What you
can expect

  • Professional Development

    Resources that promote your career growth

  • Work-Life Balance

    Leaders that support flexible work schedules

  • Growth Potential

    Clear pathways to success

  • Collaboration

    Teams that work together to achieve common goals

  • Variety

    Dynamic work environments that expose you to new experiences

  • Best-in-class Training

    Programs to help you build knowledge and gain skills

Clinical Research Associate - Ireland

Apply now
Location: Dublin, Dublin, Ireland R1212368 Posted: 10/11/2021

Job description

The IQVIA FSP team are changing the life science industry through inspired innovation. Our people make a difference. You could be part of a team that work on exciting complex studies for one single sponsor dedicated program! We are looking for experienced CRA's who care and want to make a difference in the life science industry.

The roles are home-based in any location across Ireland but we are particularly interested in hearing from candidates based in Dublin.

Responsibilities and Duties:

  • Working as a CRA you would act as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.

  • Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.

  • Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.  

  • Gains an in-depth understanding of the study protocol and related procedures.

  • Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.

  • Participates & provides inputs on site selection and validation activities.

  • Performs remote and on-site monitoring & oversight activities.

  • Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner. 

  • Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out.

  • Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance.

  • Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.

Qualifications/Skills

  • Minimum of 1 year on-site and independent monitoring experience

  • Life science degree / relevant work experience

  • Strong knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

  • Good therapeutic and protocol knowledge as provided in company training.

  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).

  • Full UK driving license with the ability to travel nationwide

#CRASDAJD 

At IQVIA, 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. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

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