Research Assistant

2 weeks ago

London, Canada Western University Full time

**About Western**:
**About Us**:
Vision

The Department of Otolaryngology - Head and Neck Surgery is to be a globally renowned Program demonstrating excellence, innovation and leadership in education, research and patient care.

Mission

To enable our Faculty to achieve their full potential, to embody pillars of strength based on core values, and to embrace a collective culture of passion to lead the cutting edge of discovery and scholarship in the context of exemplary delivery of quality care and education.

Values

Leadership, collaboration, compassion, creativity, innovation, social responsibility, excellence, quality, fairness, patient-centered and learner-focused.

**Responsibilities**:
The Research Assistant manages clinical research studies according to regulatory and institutional guidelines and requirements. This includes coordinating patient recruitment and data collection, study administration, preparing consents and paperwork required by the Research Ethics Board and organizing data entry and analysis. The RA also assists in the preparation of study results, including manuscripts, posters, and graduate theses.
- Read and have a general knowledge of protocol and study measures.
- Assist in design of case-report forms and/or questionnaires.
- Assist PI with university and hospital study review processes.
- Keep abreast of regulations and policies governing clinical research.
- Develop informed consent documents based on regulations, REB consent templates and institutional requirements. Submit to REB and coordinate revisions. Assist PI with annual approval process and amend protocols and consents as required.
- Develop study binders for clinical department and study team use.
- Encourage and foster collaborative relationships with the healthcare team at London Health Sciences Centre, other participating centres and government and community agencies.
- Participate in audits by regulatory bodies or industry sponsors.
- Conduct literature reviews and keep current with study literature.
- Assist with database design. Ensure the quality of the database and supervise database cleaning. Perform/assist with data entry and analysis.
- Assist with design/development of promotional materials/newsletters.
- Develop and monitor timelines for study.
- Provide information and documentation for potential protocol patients (consents, patient eligibility items, required pre-study testing)
- Confirm eligibility of and registering patients
- Provide feedback to patients/healthcare team and arrange clinical follow-up as required.
- Maintain budget records.

**Why Western?**:
**Background Checks**:
While transcripts are not required for the interview, the CV will be reviewed.

Consideration of applicants will include an assessment of previous performance, experience, and qualifications. Applicants should have oral communication skills in English.

**Western Values Diversity**:
**Please Note**:
We thank all applicants for their interest; however, only those chosen for an interview will be contacted.

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