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Clinical Trials jobs in Surrey, BC

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    • Familiarity with medical terminology and clinical trial protocols is beneficial.
    • Collect, record, and manage clinical data accurately and securely across…
    • The ideal candidate will work flexibly across a number of small molecule drug development programs with an emphasis on the development of in-house analytical…
    • The Patient Recruitment Specialist responsible for all recruitment related activities for assigned clinical trials.
    • Attend and report at weekly team meetings.
    • View all Headlands Research jobs - Richmond jobs - Recruiting Specialist jobs in Richmond, BC
    • Salary Search: Patient Recruitment Specialist salaries in Richmond, BC
    • As a Regulatory Affairs Specialist, Change Control, you will be responsible for assessing product, process, design, manufacturing, labeling, and documentation…
    • Order, track, and manage clinical and trial materials.
    • Minimum 3 years of experience in clinical operations.
    • Travel to clinical sites globally (50%).
    • Ensure clinical training content reflects current clinical best practices, product capabilities, and optimal workflows.
    • This is a high-autonomy role for a scientist who wants to lead, not just execute.
    • Reporting to the Director of Scientific Innovation, you'll drive the design…
    • Manages statistical activities for a clinical study or platform of clinical studies.
    • 1-3 years Demonstrated proficiency with statistical methods and…
    • Successfully humanized antibodies may enter the drug development and clinical trial pipeline.
    • A minimum of 3 year experience in the generation of stable…
    • Previous experience in clinical trials or clinical research coordination is strongly preferred.
    • Experience with sample handling for clinical trials (processing,…
    • Strong understanding of clinical workflows, patient care journeys, and healthcare delivery.
    • Support the launch of new clinical programs and treatment categories…
  • View similar jobs with this employer
    • Demonstrated understanding of clinical workflows across the care continuum.
    • The Lead provides strategic and clinical leadership to clinical planning consistent…
    • This person may work flexibly across a number of clinical stage trials and projects, acting as a study lead and manager for select clinical trial and be hands-…
    • Effectively collaborate with colleagues in Drug Product and API groups, such that deliverables are optimal for use in clinical trial material.
    • We are seeking a highly organized and detail-oriented Discovery Operations Coordinator to support our Discovery Program Management team with day-to-day…
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Job Post Details

Research Assistant - job post

Otolaryngology Clinc
Burnaby, BC•Hybrid work
$25 an hour - Part-time, Contract

Job details

Pay

  • $25 an hour

Job type

  • Part-time
  • Contract

Location

Burnaby, BC•Hybrid work

Full job description

Job Overview

We are seeking a dedicated Clinical Research Assistant to support our medical research team in conducting a long-term clinical study comparing two surgical approaches to thyroidectomy. This role involves assisting with data collection, managing research documentation, and ensuring compliance with regulatory standards. The ideal candidate will have a strong foundation in research methodologies, data management, and medical terminology, with a passion for advancing healthcare through clinical research. This position offers an excellent opportunity to gain hands-on experience in the medical research field within a collaborative and innovative environment.

Responsibilities:

  • Assist in recruiting and screening study participants according to protocol guidelines
  • Collect, record, and manage clinical data accurately and securely across multiple hospitals
  • Ensure proper documentation of all research activities and maintain confidentiality of patient information
  • Monitor participant safety and report adverse events in accordance with regulatory requirements
  • Support the preparation of study materials and assist during patient visits or procedures
  • Collaborate with research team members to ensure adherence to study protocols and timelines
  • Maintain compliance with institutional review board (IRB) regulations and Good Clinical Practice (GCP) standards

Experience:

  • Prior experience in research or clinical settings is preferred, particularly in healthcare or medical research environments
  • Knowledge of data management systems and electronic health records (EHR) is advantageous
  • Comfort with the operating room environment is required
  • Ability to commute to Burnaby Hospital and Surrey Memorial Hospital is required
  • Familiarity with medical terminology and clinical trial protocols is beneficial
  • Strong analysis skills to interpret data accurately and identify trends or discrepancies
  • Previous exposure to data collection methods, regulatory compliance, and patient interaction will enhance effectiveness in this role.

Pay: $25.00 per hour

Education:

  • Bachelor's Degree (preferred)

Language:

  • English (preferred)

Work Location: Hybrid remote in BURNABY, BC

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