Pharma Medica Research (PMRI) Inc. is a Contract Research Organization that strives for innovation and original solutions in a highly regulated and competitive industry. If your career goals align with innovation and original thinking you will be the perfect candidate to be part of an inclusive, adaptable, and forward-thinking organization. Our reputation for delivering high quality research is outstanding. At PMRI we are committed to making a difference in healthcare and people's lives. Come join our team!
We have an exciting opportunity for a Study Coordinator within our PMRI Clinic located in Scarborough, Ontario. In this role, you will contribute planning and execution of Clinical Studies. This position reports to Manager, Clinical Operations.
Duties and Responsibilities:
• Participate in planning and supervision of timely execution of studies.
• Coordinate the ordering of study-specific materials to conduct clinical studies.
• Ensure that the study schedule is prepared in compliance with the study requirements, and the study drugs are received prior to study conduction.
• Supervise and when required, assist and/or perform all technical functions: phlebotomy, ECG, vital signs and other clinical tasks to generate data in compliance with protocol, SOPs and GCP requirements.
• Perform safety-related procedures as required (e.g. conducting vital signs, electrocardiograms, concomitant medication administration) and health monitoring.
• Assist or administer certain types of investigational products as required for the conduct of a clinical study under the supervision/order of the investigator.
• Coordinate with the Project Management department regarding study related issues and project deadlines.
• Assist in resolving conflicts among subjects, ensure subject safety, and address subjects' concerns.
• Coordinate with the accounting department regarding study subjects' compensation.
• Ensure the timely shipping of the clinical and analytical samples.
• Ensure timely and accurate completion of all study-related documents and reports.
Requirements:
• B.Sc. degree with 1 year of experience in conducting clinical trials or;
• M.Sc. degree with adequate knowledge of conducting clinical trials.
• Working knowledge of Phase I study protocols and conduct.
• Understanding of the value and necessity of training and SOPs relating to study conduct.
• GCP training.
• Proficiency in computer usage and software applications.
• Ability to communicate clearly and effectively with direct reports and other clinical staff, both orally and in writing.
• Flexibility with changes in working schedules/shifts.
• Exceptional organizational skills.
We offer:
• Competitive compensation plan
• Mentorship Opportunities
• A benefit plan that is fully paid for by PMRI, including healthcare, dentalcare, vision care, LTD, Life Insurance, AD&D, along with a Health Spending and Wellness Spending Accounts and a voluntary RRSP Contribution Plan
• Opportunities for advancement and career progression
• A generous Employee Milestones Awards Program
• Corporate Discounts Program
• Learning Support Programs
• Friendly atmosphere, culture of learning
Please note all applications must be eligible to work within Canada.
PMRI is an Equal Opportunity Employer; promoting accessibility and inclusivity at work and offering accommodation for applicants as required and requested.
We thank all applicants for their interest; however, only those selected to proceed in the interview process will be contacted.
Study Coordinator • Scarborough, Ontario, Canada
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