Are you an experienced CRA looking for a more dynamic role? Join a specialized clinical research organization and work across the full trial lifecycle. As a Senior Clinical Research Associate, you'll coordinate and supervise trials at national and international sites, manage submissions, and support trial start-ups. Plus, benefit from a work-from-home allowance and employer-funded pension scheme. Read on to discover why this challenge awaits you.

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Are you an experienced CRA looking to step beyond repetitive monitoring work? Join a specialized clinical research organization where you’ll gain exposure across the full trial lifecycle, from submissions and site management to data cleaning and imaging coordination.

This is how you will make the difference

As a Sr. Clinical Research Associate, you will play a key role in coordinating and supervising clinical trials across national and international sites. Your responsibilities include overseeing site activities through a combination of on-site visits and remote monitoring, managing regulatory submissions and supporting trial start-up processes, and collaborating with local CRAs, investigators, and sponsors across multiple countries. You will also contribute to CRF design, data review, and cleaning activities, participate in sponsor and investigator meetings as well as committee support such as CEC and DSMB, and engage with internal teams—including the Core Lab—to ensure alignment across study operations.

What you bring

In order to be the next Senior Clinical Research Associate it is required to have:

minimum 4+ years of experience as a CRA in a similar clinical operations role
Strong track record in site monitoring, submissions, and site management
Experience in or familiarity within therapeutic areas—such as cardiology, oncology, or rare diseases
Strong written and verbal communication skills in English; additional EU languages are a plus
EU-based and willing to travel occasionally

What's in it for you

You’ll join a highly specialized and collaborative clinical research organization with a strong reputation in cardiology studies. The position comes with:

A flexible 36-hour workweek (with one extra day off every two weeks)
Hybrid working model – site visits count as office days
Travel reimbursement (standard allowance)
Work-from-home allowance
26 vacation days (based on a 40-hour contract)
Employer-funded pension scheme
Performance-based bonus (content-driven role focused on growth)
Training and development opportunities within a niche clinical environment

Gerelateerde zoekopdrachten

Research Associate Rotterdam Fulltime Rotterdam Vast contract Rotterdam Rotterdam Provincie Zuid-Holland Research Associate Salaris Research Associate

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