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Full-time
bachelor degree
Work-life balance, Supportive management, Professional growth opportunities
Posted 4d ago
~40 hrs/week
Remote in Belgium, Netherlands
Responsibilities
You will monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP regulations. Additionally, you will coordinate study setup activities, including identifying investigators and preparing regulatory submissions.
Requirements
Candidates must hold a life science degree and have at least 2 years of experience as a CRA in a CRO or pharmaceutical/biotech setting. Proficiency in English and Dutch is required, along with the ability to travel domestically for site visits.
Full 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 recruiting Clinical Research Associate II to join our team in Belgium. This is a remote based position primarily focused on monitoring visits in Belgium with occasional support for sites in the Netherlands.
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:
Minimum Required:
Life science degree and / or equivalent experience
At least 2 years of experience 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.
Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions)
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 and Dutch
Preferred:
Experience managing oncology studies will be a plus
Study start up activities experience.
Fluency in French will be a plus
Please apply in English.
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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].
Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at [email protected] so we can investigate and take appropriate action.
We founded Precision Medicine Group in 2012 because we believed there was a transformational opportunity to improve the process of bringing new drugs to market. It involves utilizing technology, data, and human expertise. It is a big challenge that requires diverse talents. Our model involves both nurturing and investing organically and acquiring capabilities that we do not have but critically need. Our core executive team is anchored to this model, building life science services that address fundamental changes in healthcare that are necessary for health and outcomes improvement.
Offices: 2 Bethesda Metro Center, Suite 850, Bethesda, Maryland 20814, US
Health CareBiotechnologyMedicalPrecision MedicinePharmaceutical
We founded Precision Medicine Group in 2012 because we believed there was a transformational opportunity to improve the process of bringing new drugs to market. It involves utilizing technology, data, and human expertise. It is a big challenge that requires diverse talents. Our model involves both nurturing and investing organically and acquiring capabilities that we do not have but critically need. Our core executive team is anchored to this model, building life science services that address fundamental changes in healthcare that are necessary for health and outcomes improvement.
Offices: 2 Bethesda Metro Center, Suite 850, Bethesda, Maryland 20814, US
Health CareBiotechnologyMedicalPrecision MedicinePharmaceutical