Join a dynamic, global company as a trilingual Senior CRA, where you'll be at the forefront of clinical research communication. In this role, you'll maintain relationships with clinical sites, ensure compliance with data quality, and focus on the rights, safety, and well-being of subjects. Enjoy the flexibility of a fully remote position and the opportunity to increase your workload. If you're ready to contribute to impactful research in a supportive team environment, this is your chance! Keep reading to see why we could be the perfect match for you.

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Oxford Global Resources

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Are you a trilingual Senior CRA and want to be part of a growing, dynamic, global company with a very nice familial team spirit? Don't hesitate and apply now!

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.

Responsibilities:

Your responsibilities will include:

Conducting and reporting all types of onsite monitoring visits
Driving the study startup phase (if applicable)
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

Requirements:

BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience
Independent on-site monitoring experience in Belgium, ideally on multiple projects at a time
Demonstrable experience in all types of monitoring visits in Phase II and/or III
Strong written and verbal communication skills
Fluency in Dutch, French and English
Experience supporting Oncology studies is beneficial, but not essential
Intermediate to Advanced knowledge of MS Office
Ability to plan, multitask and work in a dynamic team environment
Communication, collaboration, and problem-solving skills are essential
As you will be monitoring multiple sites, you must have a full and clean driver's license, and the ability to travel.
Existing right to work in Europe required

Contract information:

Freelancer
September start date
0.6 FTE (As of Nov/Dec possibility to increase to FT FTE)
Fully remote

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