Clinical Research Coordinator (Part-time)

Job Responsibility:
Research Coordinator With the broad and courageous vision to change how healthcare can be delivered in Canada, C-health will lead the best practice example.
Why Work Here: Great locationWork-life balanceProfessional environmentCaring LeadershipMeaningful contribution to our community and the publicGrowth & challenge
Key responsibilities: Clinical Research

• Participates in study related meetings such as site evaluations, site initiations, close-out visits, investigator meetings, monitor visits and study conference calls.
• Adheres to Standard Operating Procedures (SOPs), Internal conference of Harmonization (ICH), Good Clinical Practice (GCP), and Tri-Counsel Policy Statement: Ethical Conduct for Research Involving Humans, (TCPs) and other applicable regulator requirements.
• Prepares HREBA submissions, including informed consents.
• Creation of study documents such as source documents, screening logs and subject charts,
• Act as liaison between investigators, primary care providers and the sponsor
• Screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study
• Responsible for all data and source documentation, serious adverse event and adverse experience reporting, and maintenance of regulatory files along with any other study related duties assigned

Laboratory Oversight
~ Collect and process specimens (blood, urine, etc.) according to study protocol and laboratory manuals and procedures

• Monitors and manages laboratory supplies and inventory and equipment , including daily temperature tracking and reporting.
• Contributes to the ongoing improved operations of the laboratory by keeping current with technological developments to enhance efficiency and reliability
• Achieve and maintain IATA certification
• Participates in development and maintenance of quality control and assurance program

Qualifications:

• 1 - 3 years previous research and research administrative experience preferred
• Training in clinical trials, good clinic practice and Division 5
• Excellent interpersonal and communication skills, attention to detail, precise documentation skills and time management.
• Proven ability to strategize, plan and coordinate multiple trials and projects
• Experience in laboratory/medical environment
• Proficient in MS Office application (Word, Excel, PowerPoint and Outlook).
• Experience in Electronic Medical Records
• Ability to liaise effectively with a variety of internal and external research stakeholders

Personal Characteristics

• Highly motivated, takes initiative, demonstrates adaptability and flexibility
• Display professionalism, strong ethics, confidentiality and reliability
• Possesses a positive attitude
• Independent judgment, discretion and diplomacy
• Dedicated, personable, and confident person who is passionate about his/her career
• Makes decisions and recommendations governed by general procedures and guidelines
• Exercises independent judgment in planning, organizing, scheduling of work assignments
• Exercises initiative in adapting procedures to address unusual problems and resolves conflict

Additional Details:
We welcome applications from all qualified candidates, our workplace is as diverse as the communities we serve.
The successful candidate will be required to complete a Criminal Background check and provide record of immunizations.
Although we would love to be able to talk to every candidate, time does not permit.
Job Type: Part-time
Salary: $25.00-$27.00 per hour
Expected hours: 16 per week
Benefits:
Company events
On-site gym
On-site parking
Flexible Language Requirement:
~ French not required

Schedule:
~8 hour shift

Education:
~ Bachelor's Degree (preferred)

Experience:
~ clinical trials: 1 year (preferred)

Work Location: In person