Research Coordinator 1
3 weeks ago
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 ProfessionalAdditional 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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