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Clinical Research Assistant jobs in Toronto, ON

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    • Minimum 2-3 years of clinical research experience required.
    • Recent experience conducting clinical trials.
    • Lead clinical trial start-up work.
    • Prior experience in clinical research coordination (dermatology or clinical trial experience is an asset).
    • Coordinate day-to-day activities of clinical research…
    • Experience with an accepted clinical data capture and management system preferred.
    • Plan and manage deliverables and timelines in accordance with clinical trial…
    • The successful candidate must have a Master’s degree in psychology, neuroscience or health related field combined with two (2) years of research or clinical…
    • View all CAMH jobs - Toronto jobs - Research Coordinator jobs in Toronto, ON
    • Salary Search: Research Coordinator - Temerty Centre Research salaries in Toronto, ON
    • See popular questions & answers about CAMH
    • This position will also support across clinical research operations through the collection of data and metrics, as required.
    • Experience and certification in at least one certification in one of Epic's clinical apps (EpicCare Ambulatory, ClinDoc, Cupid, Orders, Radiant, etc).
    • Develop processes and scientific knowledge as regards clinical pharmacology aspects of clinical trials.
    • The Trial Clinical Pharmacologist (TCP) supports the…
    • Mississauga, Canada | Full time | Home-based | R1562743.
    • R1558503 Directeur associé, Relations clientèle, gestionnaire de projet – Appareils connectés / Client…
    • Research activities include clinical treatment studies, neuropsychological assessment, metabolic health research, and related clinical and translational…
    • Supporting onboarding and training of research staff (including research coordinators, research methods specialists, research analysts and research trainees).
    • 2+ years of relevant clinical research experience, including hands-on experience with clinical trial regulatory or essential documentation.
    • Prior research experience with the forensic mental health system and diverse clinical populations (e.g., inpatient psychiatric, correctional) is strongly…
    • As a physician Assistant, you will play a crucial role in providing quality patient care and assisting healthcare professionals in a clinic setting.
    • Employment Type: Full time, Permanent.
    • Responsible for the management of the Trial Master File (TMF) content and associated processes during the study life…
    • Previous experience in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry.
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Job Post Details

Clinical Trial Manager - job post

York dermatology clinic & RC
245 West Beaver Creek Road, Richmond Hill, ON L4B 1L1
$37.50–$39.50 an hour - Full-time

Job details

Pay

  • $37.50–$39.50 an hour

Job type

  • Full-time

Shift and schedule

  • Monday to Friday

Location

245 West Beaver Creek Road, Richmond Hill, ON L4B 1L1

Benefits

Pulled from the full job description

  • Vision care
  • Dental care
  • Store discount
  • Extended health care
  • Company events
  • Flexible schedule
  • On-site parking

Full job description

Job Summary:

We are looking for a permanent full-time Clinical Research Manager with extensive clinical trial management experience. We are team-oriented and believe in continued learning and professional development of all our staff. If you are highly motivated, committed to continuing professional development, work well in a team environment, have excellent communication, leadership, organizational, critical reasoning, and problem-solving skills, we want to hear from you!

Duties

  • Lead clinical trial start-up work
  • Contract preparation in collaboration with our legal partners
  • Budget preparation and negotiation
  • Creating, improving and monitoring site source documentation
  • Ethics and other regulatory submissions to Health Canada
  • Experience with site audits
  • Routine invoicing based on the approved budget
  • Responsible for coordinating and implementing all study-related activities such as initiating timely start-up, navigating strict eligibility criteria, and ensuring clean data is entered accurately and inline with monitoring requirements.

Requirements

  • Degree in sciences field, preferably biomedical science, biology, biochemistry, health systems management, statistics
  • Minimum 2-3 years of clinical research experience required.
  • Recent experience conducting clinical trials.
  • Documented experience with regulatory and ethics submissions.
  • Knowledge and ability to do budgeting and invoicing for studies that are ongoing.

Job Type: Full-time

Pay: $37.50-$39.50 per hour

Expected hours: No more than 42 per week

Additional pay:

  • Overtime pay
  • Signing bonus

Benefits:

  • Company events
  • Dental care
  • Extended health care
  • Flexible schedule
  • On-site parking
  • Store discount
  • Vision care

Flexible language requirement:

  • French not required

Schedule:

  • Monday to Friday

Education:

  • Bachelor's Degree (required)

Experience:

  • Budgeting: 2 years (preferred)
  • Data collection: 2 years (required)
  • Medical terminology: 2 years (required)

Work Location: In person

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