Clinical Research Coordinator

Canadamid

HealthcareClinical Researcher

3 views0 saves0 applied

Apply Now

Quick Summary

Technical Tools

HealthcareClinical Researcher

Clinical Research Coordinator

Non Union Technicians and Research Assistants

What We Offer

~1 min read

✓Coordinate daily study operations including monitoring recruitment progress and participant retention, identifying strategies to enhance enrollment and efficiency, obtaining consent, and visit scheduling

✓Ensure that all aspects of study are performed within International Conference on Harmonization (ICH), Good Clinical Practice (GCP) and Tri-Council guidelines, as well as institutional, site and study specific Standard Operating Procedures (SOPs)

✓Prepare research ethics submissions, maintain accurate records of REB approvals, and submit renewals and amendments as required

✓Develop study data collection forms for implementation on REDCap or other related programs

✓Develop study advertisement, promotional and instructional material for study participant recruitment. Educates study participants on protocol requirements, schedules and data collection tools.

✓Prepare and organize materials (e.g., study documents, collection kits) for initial and ongoing patient follow up study visits

✓Maintain study related documents and databases ensuring accuracy and completeness

✓Assist with blood sample collection as needed (venipuncture training provided)

✓Collect and enter research data into REDCap in a timely and accurate manner. Analyze data and prepare abstracts and manuscripts for publication for research projects as needed

✓Communicate study updates to the Translational Research Manager on a regular basis; attend bi-weekly lab meetings

✓Contribute to study reports and meeting agendas

✓Performs other related duties as required

Requirements

~1 min read

Experience in clinical research, as a research assistant or the equivalent combination of education and experience preferred
Venipuncture certification and experience is an asset
Completion of relevant clinical research courses or tutorials (i.e., TCPS 2, GCP, UBC REB) is also an asset
Experience in clinical research data collection and interacting with patient populations in a respectful and confidential manner.
Ability to communicate effectively verbally and in writing.
Effective interpersonal and problem-solving skills, and the ability to participate in a collegial manner with the team
Self-motivated with demonstrated ability to show initiative and sound judgment.
Ability to effectively use MS Word, Excel, Outlook, Internet searches at an advanced level
Experience with REDCap is an asset; experience with statistical software is an asset.
Effective critical thinking skills and understanding of complex data management principles
Ability to maintain accuracy and attention to detail
Ability to work effectively independently and in a team environment
Ability to prioritize and work effectively under pressure to meet deadlines
Ability to manage multiple tasks and assignments
Ability to supervise/mentor research assistants and students
Flexibility to adjust to scheduling changes