Research Coordinator Ii
1 week ago
Posting Period:
Open:
June 19, 2024
Deadline:
July 2, 2024
Non-Union
Job Summary:
Lawson Health Research Institute (Lawson) is the research institute of London Health Sciences Centre and St. Joseph's Health Care London.
As one of Canada's top ten research institutes, we are committed to furthering scientific knowledge to advance health care around the world.
Supported in part by the 5-year CIHR grant, RareKids-CAN will provide mentorship, guidance and oversee a part-time clinical trial navigator (CTN) at each of the 17 participating Clinical Trial Consortium sites.
Reporting to the local clinical research leadership, the CTNs will play a critical role in ensuring RareKids CAN is able to build child/family-centric research, clinical trials, and education capabilities with a focus on rare diseases.
Rate of Pay:
To commensurate with experience
Hours of Work:
Temporary Part Time - Up to 23.5 hours/week
Duration: 1 year contract with the possibility of extension
Responsibilities:
- Serve as the local point of contact for RareKids-CAN for all pediatric rare disease clinical trial inquiries.
- Liaise with local investigators/study teams to initiate a timely, and efficient study startup for rare disease pediatric clinical trials.
- Assist with industry sponsored rare disease feasibility assessments.
- Coordinate data collection locally to support quality improvement and performance metric initiatives to capture study start up timelines, and other measures of success such as the total number of rare disease clinical trials taking place and the total number of investigators involved inpediatric rare disease clinical trials.
- Participate in mentorship and training opportunities, connecting with other research institute CTNs across the country to build local capacity and expertise.
- Attend and participate in monthly meetings hosted by RareKids-CAN to share best practices and lessons learned pertaining to pediatric rare disease clinical trials.
Qualifications:
- Education required
- B.Sc, B.MSc, or B.HSc or other related field required, or relevant experience
- GCP and IATA training an asset
- Minimum 3 years clinical research experience preferred, medical research background is encouraged.
- Experience in Rare Disease Clinical Trials
- Experience with REDCap, EDC and IWRS preferred
- Knowledge and experience with study start up and feasibility assessments
- Experience in multisite clinical trials
- Experience in trials of all phases 15 an asset
- A working knowledge of LORA, REDA and WREM
- Strong communication and problem solving skills
- Ability to work in a team environment as well as independently
- Detailoriented with strong organizational skills
- Proficient time management skills, ability to meet tight deadlines
- Responsible and Selfmotivated with the ability to take initiative in an environment with limited supervision
- Strong work ethic
- Ability to follow instructions and complete assignments in a timely manner
- Available to work a flexible schedule
- Proficient in Word and Excel
- Experience with Research Ethic Board submission and correspondence, both local and central an asset
- Working knowledge or prior experience in Human Research Ethics, Tricouncil policy, Good Clinical Practices, Health Canada and FDA regulations an asset
- Excellent communication skills both verbal and written
- Experience with manuscript preparation an asset
- Demonstrated knowledge of and commitment to patient and staff safety at LHSC
- Demonstrated ability to attend work on a regular basis
Immunization Requirements:
Before beginning employment at LHSC, all new hires will be required to:
- Provide vaccination records or proof of immunity against measles, mumps, rubella and varicella (chicken pox), Hepatitis B, Tetanus/ Diphtheria/Polio; Meningitis;
- Provide documentation of the Tuberculosis skin testing (two step);
- Provide proof of Health Canadaapproved COVID19 vaccination reflective of Ontario Health's current definition of being fully vaccinated
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