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
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