Clinical Research Associate (no travel) at IQVIA
Werk van thuis, , Netherlands -
Full Time


Start Date

Immediate

Expiry Date

20 Jul, 25

Salary

0.0

Posted On

14 Jun, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Hospital/Health Care

Description

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

CLINICAL FSP BUSINESS

IQVIA clinical FSP business is unique. Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our clients. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study.
We are recognised as one of the most admired companies in the world to work for by Fortune magazine. The reason we have continually received this accolade is our commitment to continued growth and development.
We understand that everyone looks for new opportunities for different reasons, within our Dutch team we aim to make sure you have a job you are happy with and not just a job. Are you looking for a role with reduced travel, a homebased role, continued training, locally based manager, and a structured career path? We will work with you during the recruitment process to understand what is important to you.

Responsibilities

ROLE DETAILS:

  • Working in partnership with a single-sponsor
  • No site visits with no travel
  • All CRAs and SCRAs are allocated a dedicated IQVIA Line Manager
  • Fantastic work/life balance

RESPONSIBILITIES:

  • Site management and monitoring activities across the country
  • Work with sites to adapt, drive and track subject recruitment plan
  • Provide protocol and study training to the assigned sites
  • Create and maintain monitoring visit reports and action plans
  • If appropriate, co-monitor, train and mentor junior members of the team
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