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Clinical Associate, Baylis Medical $70,000 jobs

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    • Excellent knowledge of medical terminology and clinical monitoring process.
    • Experience with clinical trial information systems.
    • Fluent in French and English.
    • Program or Project Management Experience.
    • An experienced Epic Clinical Associate Manager or Manager.
    • Bachelor’s degree or completion of a college program in a…
    • Have graduated from an accredited DDS/DMD or equivalent program and have relevant postgraduate and clinical qualifications in the specialty of prosthodontics.
    • Have graduated from an accredited DDS/DMD or equivalent program and have relevant postgraduate and clinical qualifications in the specialty of periodontology or…
    • Experience providing psychotherapy, counselling, or structured clinical support under supervision.
    • A Master’s degree in clinical psychology, counselling…
    • Previous research or service experience with individuals and/or families with mental health and addictions issues is an asset.
    • Upon arriving to work in the morning, you will provide direct clinical care to patients on 20 or 40 minute appointments..
    • Sick leave and bereavement leave.
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    • Demonstrated competency to perform complete and appropriate clinical assessment and development of a treatment plan in accordance with medical directives.
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    • Act as a clinical and information resource to the psychiatry team including nursing, clerical, residents, medical students, and other members.
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    • Demonstrated competency to perform complete and appropriate clinical assessment and development of a treatment plan in accordance with medical directives.
    • Doctoral degree (Ph.D. or Psy.D.) in Clinical, School, or Educational Psychology.
    • Master's degree or Doctorate in Psychology.
    • Job Types: Part-time, Contract.
  • View similar jobs with this employer
    • Demonstrated competency to perform complete and appropriate clinical assessment and development of a treatment plan in accordance with medical directives.
  • View similar jobs with this employer
    • Demonstrated competency to perform complete and appropriate clinical assessment and development of a treatment plan in accordance with medical directives.
    • The supervising physician is responsible for the medical care provided to the patient by the PA and can only delegate medical acts that are within their own…
    • Reporting to the Chief and Medical Director of Emergency Department, and working closely with the existing Physician Assistant team, under the direction and…
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Job Post Details

Clinical Research Associate-Freelance - job post

Translational Research in Oncology
4.0 out of 5 stars
Remote
Temporary
You must create an Indeed account before continuing to the company website to apply

Job details

Job type

  • Temporary

Full job description

Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.

TRIO is seeking a Clinical Research Associate (CRA) to join our Monitoring Resource team. This is a remote, part-time freelance opportunity on a 6-month contract, open to candidates based in Canada.

Responsibilities:
  • Performing data verification of source documents;
  • Conducting site visits, including pre-study, initiation, monitoring, and termination;
  • Confirming adherence to all FDA, ICH-GCP, and local regulations;
  • Ensuring implementation and compliance with FDA, and ICH-GCP guidelines
  • Participating in budget negotiation and follow-up where applicable
  • Assisting with data validation and query resolution
  • Mentoring junior team members as required
  • Ensuring the completion and collection of regulatory documents
Qualifications:
  • A minimum of 2 years of monitoring experience in oncology trials
  • Fluent in French and English
  • Experience monitoring in early-phase trials will be valued.
  • Completion of a science-related Bachelor’s degree
  • Excellent knowledge of medical terminology and clinical monitoring process
  • Strong ICH-GCPs knowledge
  • Experience with clinical trial information systems
  • Ability to travel up to 60% on average
  • Must be legally authorized to work in the country


Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.

Prior to applying please review TRIO's Applicant Information Notice

To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI.

To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience.

Teamwork · Passion · Integrity · Innovation

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