Study Participant Recruitment
Establish recruitment needs and timelines for each study and advise Lead Investigator on the availability of potential study participants.
Develop recruitment strategies and required documents, including study-specific promotional material and advertising, in accordance with research ethics standards.
Establish contact with potential study participants and direct them toward the appropriate study.
Ensure recruitment targets are being met, advise researchers of recruitment status and re-evaluate accordingly.
Gather participant feedback in order to improve their experience.
Building Community Awareness
Through market research, gain an understanding of the sociologic characteristics of the community and use that information to develop strategic marketing-promotional plans.
Develop, implement and monitor specific marketing initiatives including outreach events.
Maintain responsibility for the recruitment discretionary fund as assigned by the CCLR Senior Admin Team.
Build relationships with potential study participants, local optometrists and community organizations.
Co-op Student Management
Participate in the hiring, training and evaluation of the Recruitment/Research Assistant Co-op student.
Manage day-to-day tasks of the Co-op student.
Website and Social Media Management
Develop content and promotional material for the participant portal in accordance with research ethics standards.
Upload and manage material, reviewing for consistency.
Manage the CCLR social media platforms.
Work with external contractors on the management of the CCLR website and other supported websites as required.
Study Participant Data Management
Maintain CCLR Pre-Screening study participant database by inputting and updating information.
Monitor database for gaps in participant demographics.
Manage study participant agreements specifying the use and confidentiality of their recruitment data.
Query database to match potential participant characteristics with study inclusion criteria.
Treat and use participant information in a confidential and sensitive manner according to clinical trial regulations and University policies.