Clinical Research Coordinator - Nijmegen

Hobson Prior

Nijmegen

On-site

EUR 35,000 - 50,000

Full time

14 days+

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Job summary

A leading company is seeking a Clinical Research Coordinator in Nijmegen to support clinical trials in the cardiovascular field. The role involves managing research activities, ensuring protocol compliance, and liaising with patients. This six-month contract position offers flexible hours, focusing on patient care and coordination.

Qualifications

Strong experience in clinical research coordination required.
Excellent organizational and communication skills are a must.
Familiarity with clinical trial protocols and regulatory compliance.

Responsibilities

Inform patients about clinical trial details and eligibility.
Review medical histories to determine eligibility.
Plan and coordinate research activities with specialists.

Skills

Clinical research coordination

Organizational skills

Communication skills

Attention to detail

Regulatory compliance

Job description

Clinical Research Coordinator - Nijmegen

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Senior Consultant – Clinical Operations and Development Switzerland & EU at Hobson Prior

Make your mark in global health by managing high-impact clinical trials with a leading CRO.

Hobson Prior is seeking a Clinical Research Coordinator to join a dynamic team in Nijmegen, Netherlands. This role focuses on supporting clinical trials in the cardiovascular field. You will play a key part in ensuring the smooth execution of research activities, patient coordination, and compliance with protocols. This is a contract position for at least six months, requiring 24 hours per week.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

Inform patients about the clinical trial, including assessments, procedures, and eligibility criteria.
Review patient medical history and test results to determine eligibility based on protocol requirements.
Plan and coordinate research activities, including scheduling appointments with physicians and specialists.
Manage logistics such as transporting biological materials and ensuring timely medication supply.
Monitor the quality and progress of the clinical trial across hospital departments.
Act as the main point of contact for study participants, addressing medical complaints and guiding them through the trial process.
Provide support and education to patients and their families throughout the trial.
Ensure compliance with local procedures, regulations, and instructions, addressing any concerns.
Serve as the first point of contact for sponsor monitors and facilitate monitoring visits or audits.
Perform administrative tasks, including data entry into trial-related systems.

Key Skills and Requirements:

Strong experience in clinical research coordination.
Excellent organizational and communication skills.
Ability to manage multiple tasks and maintain attention to detail.
Familiarity with clinical trial protocols and regulatory compliance.
Proficiency in administrative and data entry tasks.

For more information, please contact Elliott Croft.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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