ClinChoice
Clinical Research Associate II or Senior Clinical Research Associate
ClinChoice, Sauk Trail Beach, Wisconsin, United States
Clinical Research Associate II or Senior Clinical Research Associate
Are you a CRA looking for the best of both worlds? Would you like to work directly with a single sponsor while still enjoying the stability, global reach, and career development opportunities that come with working for a leading CRO? Our team calls it the best of both worlds — and we think you’ll agree.
ClinChoice is a rapidly growing global contract research organization. We’re currently expanding our CRA network in Belgium and are seeking skilled Clinical Research Associates (CRA II or Senior CRA) interested in partnering with some of the world’s leading pharmaceutical companies in the field of biomedicine.
If that sounds like you, we encourage you to submit your resume via our website — we’d love to hear from you!
As a CRA, you’ll manage clinical study activities across multiple sites within one or more projects, with a focus on medical devices. You will oversee site performance, conduct company-initiated clinical studies, and ensure high-quality deliverables through site visits, monitoring, and effective communication.
Key Requirements
Willingness to travel to sites and surrounding countries (50-80% travel).
Fluent in English and Dutch.
Prior experience in monitoring clinical trials and site management.
Skills and Qualifications
• Bachelor’s degree or equivalent in a scientific or medical discipline (Nursing, Life Sciences, etc.).
• Up to 8 years of experience as a CRA.
• Strong knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirements.
• Sound knowledge of medical terminology.
• Proficiency in Microsoft Office (Word, Excel, Outlook).
Education and Experience
• Bachelor’s degree (Life Science, Physical Science, Nursing, Biological Science) or higher (Master’s, PhD, MD).
• Minimum 4 years of onsite monitoring experience.
• Previous medical device monitoring experience required; therapeutic area experience in neuro‑ or cardiovascular domain preferred.
• Relevant industry certifications preferred (CCRA, RAC, CDE).
The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it. If you meet the requirements, you will be invited for a phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for? ClinChoice is a global full‑service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high‑quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia‑Pacific.
Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly‑qualified personnel.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
Keywords Senior Clinical Research Associate, Senior CRA, Freelance, Self‑employed, Contract, Site Management, Monitor, Monitoring, Complex Trials, Medical Devices, Cardiology, Neurology, Open to Travel, Submissions, Ethics, Contract Research Organisation, CRO
Apply for this job Apply for this job via our website or contact ClinChoice directly.
#J-18808-Ljbffr
ClinChoice is a rapidly growing global contract research organization. We’re currently expanding our CRA network in Belgium and are seeking skilled Clinical Research Associates (CRA II or Senior CRA) interested in partnering with some of the world’s leading pharmaceutical companies in the field of biomedicine.
If that sounds like you, we encourage you to submit your resume via our website — we’d love to hear from you!
As a CRA, you’ll manage clinical study activities across multiple sites within one or more projects, with a focus on medical devices. You will oversee site performance, conduct company-initiated clinical studies, and ensure high-quality deliverables through site visits, monitoring, and effective communication.
Key Requirements
Willingness to travel to sites and surrounding countries (50-80% travel).
Fluent in English and Dutch.
Prior experience in monitoring clinical trials and site management.
Skills and Qualifications
• Bachelor’s degree or equivalent in a scientific or medical discipline (Nursing, Life Sciences, etc.).
• Up to 8 years of experience as a CRA.
• Strong knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirements.
• Sound knowledge of medical terminology.
• Proficiency in Microsoft Office (Word, Excel, Outlook).
Education and Experience
• Bachelor’s degree (Life Science, Physical Science, Nursing, Biological Science) or higher (Master’s, PhD, MD).
• Minimum 4 years of onsite monitoring experience.
• Previous medical device monitoring experience required; therapeutic area experience in neuro‑ or cardiovascular domain preferred.
• Relevant industry certifications preferred (CCRA, RAC, CDE).
The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it. If you meet the requirements, you will be invited for a phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for? ClinChoice is a global full‑service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high‑quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia‑Pacific.
Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly‑qualified personnel.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
Keywords Senior Clinical Research Associate, Senior CRA, Freelance, Self‑employed, Contract, Site Management, Monitor, Monitoring, Complex Trials, Medical Devices, Cardiology, Neurology, Open to Travel, Submissions, Ethics, Contract Research Organisation, CRO
Apply for this job Apply for this job via our website or contact ClinChoice directly.
#J-18808-Ljbffr