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Open nowPosted 2 days ago

Senior Clinical Research Associate

EURES job mobility portal314,718 open roles

Where
Zuid-Limburg, Netherlands
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Your applicationOpen nowSenior Clinical Research AssociateEURES job mobility portal · Zuid-Limburg, Netherlands

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  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

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The clock on this job

Early applications get read.

7.8% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 1.7%1 day
  2. 3.5%3 days
  3. 7.8%7 days
  4. 14.6%14 days
  5. 34.1%30 days
This job: posted 2 days ago

The posting

BeBee Academy & AI Juridisch Profiel Nederland - Senior Clinical Research Associate Healthcare PSI CRO Vandaag Tot 29-3-2027 Voltijd Volledig remote Pas mijn cv aan voor deze vacature Functieomschrijving PSI is a leading Contract Research Organisation with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. Your focus will be on subjects' rights, safety and well-being and quality of data compliance. This is a home-based position. Your responsibilities will include - Conducting and reporting all types of onsite monitoring visits - Driving the study startup phase - Performing CRF reviews, source document verification and query resolution - Be responsible for site communication and management - Supervising study activities, timelines, and schedules for each site - Acting as a point of contact for in-house support services and vendors - Supporting quality control, such as compliance monitoring and reports review - Participating in feasibility research - Supporting the regulatory team in preparing documents for study submissions and regulatory approval Qualifications - BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience - Independent on-site monitoring experience in the Netherlands - Demonstrable experience in all types of monitoring visits in Phase II and/or III - Strong written and verbal communication skills - Fluency in Dutch and English - Experience supporting Oncology studies is beneficial, but not essen...

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