Research Coordinator 1

Responsibilities include but are not limited to : Responsibilities include but are not limited to :

• Serve as primary contact for multiple studies / sites
• Recruit and screen patients for eligibility for current studies based on established protocols
• Conducts and documents informed consent process
• Monitor subject’s progress and report adverse events
• Generate study specific case report forms (CRFs)
• Record study data into CRFs, query resolution and responding to data queries
• Manage Research Data Bases
• Maintain Clinical Trial Management System
• Prepare for and conduct study monitor visits and audits
• Serves as a liaison to physicians, investigators, patients and other staff members regarding the research process and individual protocols
• Submit and Review Institutional Review Board documents
• Strategizes and helps troubleshoot to correct problems
• Escalates issues as needed to supervisor

Qualifications include but are not limited to :

• Clinical Research Experience (2+ years)
• Current GCP and familiarity with Health Canada, FDA, ICH GCP regulations
• Current GCP, Health Canada Part C Division 5, IATA certifications
• Bachelor’s Degree or 4 years relevant professional experience in lieu of degree
• Experience with Microsoft Office (Word, Excel, Power point, etc.)
• Have a true passion to work in Clinical Trials
• Phlebotomy certification
• Comfortable in the lab setting (Centrifuge / pipetting)

Required Skills :

• Excellent organization and attention to detail
• Quick and eager learner
• Ability to work independently
• Strong critical thinking
• Excellent oral and written communication
• 2+ years of experience in related field
• Working knowledge of research methodology / medical terminology
• Meticulous work ethic and attention to detail, with excellent time-management and organizational skills.
• Ability to manage competing demands of short and long-term projects led by numerous individuals, directing multiple varied assignments, independently coordinating and prioritizing relevant projects, tasks and responsibilities.
• Highly motivated and adaptable with an ability to take initiative and work well independently and as part of a multidisciplinary team.
• Ability to produce high quality work while meeting deadlines in accordance to CTU standards.
• Ability to maintain confidentiality.
• Certification as a Clinical Research Professional

Additional Benefits :

• 4% Vacation
• Opportunity to enroll in the Healthcare of Ontario Pension Plan (HOOPP)
• Access to 24 / 7 Employee Assistance Program
14 days ago