Clinical Research Coordinator II - SHNRI Operations (GEN)

Scarborough Health Network • Granbury, TX

1d • $40 - $46 • Onsite

About The Position

Position Overview: SHN Research Institute: With a deep commitment to fostering a stronger culture of research and innovation, and with the aim of establishing leadership in population health and health equity research, Scarborough Health Network (SHN) has established an independent Research Institute (SHNRI). The vision and mission for Scarborough Health Network’s Research Institute (SHNRI) are reflective of an ambitious research mandate, the unique strengths of SHN and the community it serves. Vision: Better health through research that matters to our community. Mission: To partner with our diverse communities to generate and apply new knowledge and innovative solutions that make healthcare more equitable, accessible and relevant. A key commitment for SHNRI will be to support the translation and application of research findings, solutions and other evidence-based knowledge into policy and practice. Bringing expertise and resources in the science of implementation, the Research Institute will support clinical teams, community partners, policymakers and other stakeholders in translating research into impact. The successful candidate reports to the SHNRI Research Manager and would provide support to various research projects. They will work with Principal Investigators to assist with participant recruitment, conduct of study activities, study documentation (including ethics submissions and communications), contract and finance submissions, collection and maintenance of data, data processing and analysis, study coordination and preparation of presentations and manuscript submissions, and documentation control.

Requirements

• 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
• 3-5 years of experience and education with relevant clinical experience and training
• Experience in a hospital setting
• Experience with clinical trial recruitment, patient screening, study processes, and REB submissions
• Strong data management skills with experience in the use of computer software applications, including Microsoft Office programs, data collection and analysis software
• Excellent knowledge of Good Clinical Practice, Ethics, Quality and Risk Management
• Excellent communication (verbal/written) and interpersonal skills are necessary
• Strong initiative, attention to detail, interpersonal, proactive and highly resourceful
• Able to work independently and as part of a team
• Able to cope with pressures and deadlines while adapting to evolving processes and procedures
• This position plays a critical role in acting as an advocate for safety and will demonstrate principles, practices and processes that will optimize a safe environment for all

Nice To Haves

• Master’s or currently enrolled in a masters is an asset
• Experience with grant writing, review, and administration
• Experience coordinating randomized clinical trials or related research experience required

Responsibilities

• Oversee all study participant recruitment activities
• Perform Screening and conduct study activities
• Conduct interviews, questionnaires, surveys and focus-groups
• Manage REB submissions
• Ensure project deadlines are met and communicated to project teams through meetings, email communications, and task updates
• 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
• Manage study start-up and close-out/archiving activities
• Assist with contracts and finance related paperwork
• Perform collection, transcription and entry of study related data
• Liaise with study stakeholders and represent team as directed by PI
• Ordering supplies and maintaining inventory
• Perform data processing and analysis
• Prepare and submit presentation and manuscripts
• Assist with grants e.g. administrative tasks, review, writing
• Perform clinical tasks, as trained and delegated, by PI/Management and noted in Protocol and source/CRF/eCRF e.g. vitals, AE data collection, phlebotomy, etc.

Benefits

• Defined Benefit pension plan through the Healthcare of Ontario Pension Plan
• Comprehensive insured benefits package including health and dental benefits
• New Graduate Initiative
• Enroute Program
• Critical Care Sponsorship Program
• Employee Discount and Incentive Programs
• Employee and Family Assistance Program (EFAP), along with other comprehensive wellness offerings, including our Spiritual Care team of registered psychotherapists for spiritual, religious or emotional care; mental health supports; and on-site wellness rounding
• Recognition events
• Leadership Development and Learning Programs
• Tuition Assistance Program

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level