Clinical Research Coordinator

Hobson Prior International Ltd; Northwestern Ontario; On-site; CAD 60,000 - 80,000; Full time

Job summary

Join a leading pharmaceutical company as a Clinical Research Coordinator, where you'll manage clinical research studies and ensure compliance with protocols. This role requires strong organizational skills, the ability to work independently, and a background in clinical research. You'll play a vital role in healthcare innovation through impactful research.

Qualifications

• Experience in clinical research coordination and phlebotomy required.
• Ability to work with diverse teams and effectively communicate.
• Strong leadership and organizational skills emphasized.

Responsibilities

• Screen and enroll participants for clinical studies.
• Monitor study participants for adherence to protocols.
• Prepare and manage study documentation and materials.

Skills

Understanding of medical and research terminology

Familiarity with clinical trial regulations

Strong communication skills

Excellent organizational abilities

Problem-solving skills

Professional demeanor

Education

Bachelor's Degree or equivalent experience

Tools

Clinical trial databases

Job description

Help bring science to life and join a leading pharmaceutical company to play a key role in delivering impactful research that drives healthcare innovation!

Hobson Prior is seeking a Clinical Research Coordinator to join our client's team in Canada. In this role, you will be responsible for managing clinical research studies, ensuring compliance with protocols and regulations, and working closely with study participants. This position requires strong organizational skills and the ability to work independently in a fast-paced environment.

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

Responsibilities:

• Screen and enroll participants for clinical studies.
• Monitor study participants and ensure adherence to study protocols.
• Prepare and manage study documentation and materials.
• Coordinate with investigators and site staff to discuss study requirements.
• Assist in recruiting study participants and maintaining effective communication with them.
• Conduct basic clinical procedures like blood draws and vital signs.
• Review and record study data accurately and promptly.
• Identify and report any adverse events during the study.
• Support regulatory processes and documentation.

Key Skills and Requirements:

• Understanding of medical and research terminology.
• Familiarity with clinical trial regulations and good clinical practices.
• Strong communication skills and ability to work with diverse teams.
• Excellent organizational and leadership abilities.
• Proficiency in using clinical trial databases and software.
• Ability to think critically and solve problems effectively.
• Friendly and professional demeanor with a positive attitude.
• Bachelor's Degree preferred or equivalent experience.
• Experience in clinical research coordination and phlebotomy.

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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