Clinical Research Associate – Open Application
Are you ready to contribute to the successful delivery of clinical trials from site selection through close out? As a Clinical Research Associate within the MindCapture network, you are considered for future CRA assignments at leading pharmaceutical biotechnology and medical device organisations. You operate at the intersection of patient safety data quality and GCP compliance, with a strong focus on site management and trial execution.
What is offered
Ready to grow your career and make real impact? Join MindCapture.
We offer two collaboration options and you can choose what fits you best.
As an employee
You receive a competitive salary package with meal vouchers eco vouchers DKV health insurance group insurance net expense allowance and company car options. You benefit from personalised training coaching and a clear long term development path within Clinical Operations.
As a freelancer
You work in a transparent collaboration model with competitive daily rates long term projects and professional support from MindCapture.
In both cases, you work as a MindCapture consultant and get matched with CRA opportunities that align with your experience level and therapeutic interests.
Job description
As a CRA in our network you may be matched to assignments such as:
* Prepare and conduct site qualification initiation monitoring and close out visits
* Ensure protocol adherence GCP compliance and patient safety at site level
* Train site staff on study procedures and provide continuous study support
* Review source data and verify data quality through SDV and risk based monitoring
* Manage site performance including recruitment timelines deviations and issue resolution
* Follow up action items and drive timely closure of findings CAPAs and queries
* Maintain essential trial documentation including TMF updates visit reports and tracking logs
* Collaborate with study teams vendors and investigators to ensure smooth trial delivery
* Support audit and inspection readiness by maintaining compliant documentation and processes
Requirements
* Degree in Life Sciences, Nursing, Pharmacy or related field
* Experience in clinical research as CRA in house CRA study nurse or CTA is an advantage
* Good knowledge of ICH GCP and clinical trial processes
* Strong organisational skills with the ability to manage multiple sites and priorities
* Clear communication skills and confidence in stakeholder management with sites
* Detail oriented mindset with focus on data integrity and quality
* Willingness to travel depending on project scope
* Fluent in English, Dutch and French are strong assets
* Experience with CTMS EDC and TMF tools is a plus
Are you ready to make a real difference in clinical research?
Join our dynamic team and help deliver clinical trials that improve patient lives.
Apply now and let’s make an impact together.
Want to learn more? Discover all opportunities at www.mindcapture.com