Clinical Research and Trials Coordinator
3 days ago
**In this role, you will**:
- Participate as a part of an interdisciplinary team and coordinate clinical trial activities to ensure that the objectives of the clinical trial are met.
- Collaborating with the Qualified Investigator/Principal Investigator, Manager, or designate, assist with preparing documentation required for ethics review and organize relevant material required for internal and external audits and inspections.
- Coordinate, organize and perform special work assignments and projects, including chart reviews, database development and surveys, to ensure the objectives of the assignments/projects are met as directed by the Qualified Investigator/Principal Investigator, Manager or designate.
- Prepare, organize and maintain clinical trial research activities and assist the Qualified Investigator/Principal Investigator, Manager, or designate with financial tasks for trials or research studies in collaboration with the Clinical Trials Unit.
- Respond to research cancer patient referrals, connect with patients by phone or in-person to assess their consent status, and consent patients for research studies.
- In collaboration with the Clinical Trials Team, determine the data requirements for specific projects, coordinate the data capture activities and capture the clinical trials data according to the study protocol or project specifications.
- Assist in the planning of pilot studies, in consultation with the Qualified Investigator/Principal Investigator, Manager, or designate, by providing information to assist in the determination of study feasibility, including issues related to possible study costs, time requirements, resource implications, quality of data and ease of data capture.
- In collaboration with the Qualified Investigator/Principal Investigator, Manager, or designate, complete and submit documents for BC Cancer Research Ethics Board review and maintain ongoing ethics-approved research protocols as required by the BC Cancer Research Ethics Board. Submit adverse event reports, amendments, annual renewals and general correspondence as required.
- Maintain knowledge of current developments in research studies through activities including reviewing relevant literature, consulting with other professionals and attending relevant education programs as requested and approved by the Qualified Investigator/Principal Investigator, Manager or designate. Conduct medical literature searches and literature reviews as required. Prepare a variety of reports for the Qualified Investigator/Principal Investigator, Manager or designate.
- Promote research studies to patients, families and health care professionals; update webpage, share information in newsletters.
- Perform data capture, management, retrieval and analysis using an automated information system.
You have:
- A level of education, training and experience equivalent to a Bachelor's of Biology or Physiology degree or other relevant healthcare discipline
- Relevant clinical reseach knowledge
- Computer skills, including the ability to work in an intermediate Microsoft Office environment utilizing a wide variety of software
- Demonstrated ability to work independently and prioritize work.
- **###**:
- **Employment Status**:
- **Wage: $30.75-38.33 Hourly**:
- **Working Schedule**:
- **Address**
**ATTN: PHSA Employees**:
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