POSITION:

Clinical Research Coordinator
2 positions (Full -time)
1 Contract position (6 months)

LOCATION:

Biovail Contract Research

REPORTING TO:

Supervisor, Study Management

POSITION DESCRIPTION:

• Responsible for the coordination of studies throughout each clinical stage. 
• Monitor and track progress and execution of each study to ensure compliance with client timelines, study protocol, company SOP’s GCP and applicable regulatory requirements
• Act as project leader for assigned studies, coordinating all clinical activities throughout each stage of the project (from study planning, implementation through to completion).
• Track performance of each study with respect to established timelines and compliance measures
• Identify, investigate and appropriately address non-compliance issues as they occur during the conduct of the study
• Supervise all study related procedures to ensure they are carried out as specified in the study protocol and SOP’s
• On call as needed to respond to medical or operational emergencies
• Write and review SOPs, directives and study specific documents

QUALIFICATIONS & EXPERIENCE:

• Bachelor’s degree or Master’s in a related field of Science  (BSc or RN)
• Medical or pharmaceutical experience is necessary with relevant clinical experience or 2-3 years experience in clinical research (Bioequivalence, Phase I)
• CCRP certification an asset
• Detailed oriented
• Basic knowledge of GCP
• Excellent communication and interpersonal skills
• Able to work under pressure as well as to adapt to changing priorities
• Ability to accommodate a flexible work schedule
• Strong team player

THIS POSITION REQUIRES WEEKEND AVAILABILITY

Please apply at: jobs@biovail.com

Biovail Contract Research is an equal opportunity employer. We thank all applicants for their interest; however only those selected for an interview will be contacted.