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

Hobson Prior is seeking a Site Manager to oversee daily operations at clinical research sites. In this role, you will ensure smooth execution of clinical trials, manage challenging protocols, and maintain compliance with regulatory standards. You will also mentor team members, perform clinical tasks, and collaborate with stakeholders to meet enrollment goals. This position requires on-site work with regional travel.

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

Responsibilities:

• Supervise daily site activities under the guidance of the Regional Manager.
• Mentor and support clinical research staff to ensure they understand processes and succeed in their roles.
• Screen potential study participants and obtain informed consent.
• Perform basic clinical procedures such as blood draws, vital signs, and ECGs.
• Review test results for accuracy and escalate any concerns to investigators.
• Identify and report adverse events (AEs) and serious adverse events (SAEs).
• Manage complex protocols and act as the primary contact for therapeutic areas.
• Administer investigational products and monitor participants for reactions.
• Maintain accurate records, including medication inventory and compliance data.
• Ensure adherence to Health Canada regulations and Good Clinical Practices (GCP).
• Collaborate with investigators to review protocols and resolve data queries.
• Support regulatory documentation and maintain study blinding when required.
• Foster positive relationships with participants, sponsors, and team members.
• Optimize recruitment efforts to meet enrollment targets.

Key Skills and Requirements:

• Strong knowledge of medical and research terminology, federal regulations, and GCP.
• Ability to mentor and guide less experienced team members.
• Excellent organizational, leadership, and communication skills.
• Proficiency in clinical trial databases, electronic data capture systems, and MS Office.
• Critical thinking, problem-solving, and attention to detail.
• Friendly and professional demeanor with the ability to work under pressure.
• Recent experience in phlebotomy and clinical research coordination.
• Preferred qualifications: RN or LPN/LVN certification, research certification (e.g., CRCC), and a bachelor's degree or equivalent experience.

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.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.hobsonprior.com/privacy-policy.