Research Coordinator Ii

2 weeks ago


Toronto, Canada St. Michael's Hospital Full time

**Here’s what you’ll get to do**:
We work in a hybrid environment, working both remotely and on site as tasks require.

**Duties & Responsibilities**:
**Responsibilities include, but are not limited to**:

- Conduct follow-ups with participants, research teams, and sites as needed
- Coordinate RedCap database development for clinical trials/studies
- Assist in the design, development, and implementation of research protocol, including designing and delivering training of protocol components to the study team.
- Assist in analysis plans for administrative health data, including electronic medical records
- Prepare research and progress reports/presentations for funders, and various stakeholders
- Liaise between research teams, stakeholders, trainees and community partners
- Ensuring appropriate regulations and policies are adhered to in the conduct of research
- Other assigned duties, as required

**Qualifications and Skills**:

- Undergraduate Degree in Health Science or a related field of study and 3 years of relevant experience, OR demonstrable equivalent combination of specialized education and experience.
- Experience coordinating randomized clinical trials or related research experience required
- Excellent knowledge of Good Clinical Practice, Ethics, Quality and Risk Management
- SoCRA or ACRP certification an asset
- Familiarity with RedCap and RAVE databases is beneficial
- Effective interpersonal skills as a member of a high-functioning team
- Excellent oral and written communication skills
- Strong analytic and problem solving skills with the ability to provide close attention to detail
- Must be computer literate (good typing skills and demonstrated proficiency of computer software programs such as MS Office)
- Proven ability to multi-task, prioritize work effectively and meet multiple deadlines

**18 month contract **_(maternity leave coverage)_**; modified benefits



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