Clinical Research associate II New Brussels, Belgium, Belgium

Precision Medicine Group; Brussel Hoofdstad; Hybrid; EUR 52,000 - 78,000; Full time

Job summary

Precision Medicine Group is recruiting a Clinical Research Associate II for Belgium or the Netherlands. This remote-based position requires monitoring oncology studies with up to 50-60% travel, based in Belgium or the Netherlands.

You will be involved in site visits, regulatory submissions, and study setup while maintaining high-quality data and timelines. Ideal candidates hold a life science degree with at least two years as a CRA in CRO or pharma, and are fluent in English and Dutch (French a

Qualifications

• Life science degree or equivalent experience in clinical research.
• Minimum 2 years as CRA in CRO or pharma/biotech, with oncology studies experience.
• Fluency in English and Dutch; French a plus.

Responsibilities

• Monitor and own the progress of clinical studies at investigative sites ensuring adherence to protocol, SOPs, ICH-GCP and regulations.
• Coordinate study setup and monitoring activities (identify investigators, regulatory submissions, pre-study and initiation visits).
• Assist with regulatory submissions and site visits as needed to support trial execution.

Skills

Oncology monitoring

Communication skills

Travel readiness

Attention to detail

Client-focused

Team player

English & Dutch fluency

Education

Life science degree

CRO/pharma experience

Job description

Precision for Medicine is not your typical CRO.At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease.

We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result.Most meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.

We are now recruitingClinical Research Associate II to join our team in Belgium or the Netherlands. This is a remote based position with travel to sites for morning visits. We are looking for candidates based in Belgium or the Netherlands with oncology monitoring experience.

About you:

• You are calm, thoughtful, and responsive when things don’t go as planned.
• You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
• You find quick and creative ways of overcoming difficulties.
• You have an impeccable eye for detail.
• You identify potential study risks and propose solutions on how to mitigate them.
• You take responsibility in the quality and outcomes of your work.
• You are adept at handling conflict by using tried and true resolution strategies.

How we will keep you busy and support your growth:

You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).

Qualifications:

• Life science degree and / or equivalent experience
• 2 years or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies. Site management or equivalent experience in clinical research.
• Experience managing oncology studies

Other Required:

• Excellent communication and organizational skills are essential. A team player.
• Evidence of a client focused approach
• Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions)
• Fluency in English, Dutch
• French will be a plus

Preferred:

• Study start up activities experience.

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