Research Manager Cheo Ri - Ottawa, Canada - CHEO
Description
Compensation Pay Range:
$0.00-$0.00
Job Description:
Posting #RI-24-013
Posting Period - March 21 to April 4, 2024
POSITION:
Research Manager - Canadian Donation and Transplantation Research Program
TERM:
1.0 FTE. 1 year contract with possibility of renewal
SALARY:
Will commensurate with skills and experience with a range of $60,000- $80,000 plus benefits.
REPORTS TO:
Dr. Sonny Dhanani
Children's Hospital of Eastern Ontario Research Institute ("CHEO RI") is the research arm of the Children's Hospital of Eastern Ontario - Ottawa Children's Treatment Centre ("CHEO") and an affiliated institute of the University of Ottawa.
CHEO RI works to create new knowledge and evidence to support CHEO in its provision of world-class care to our children.
Our mission at CHEO RI is to connect exceptional talent and technology in pursuit of life-changing research for every child, youth, and family in our community and beyond.
CHEO RI has an immediate requirement for a Research Manager.The Canadian Donation and Transplantation Research Program (CDTRP) is currently recruiting a full
- Research Services Manager to join our team. Our organization's mission is to drive advances in Canadian donation and transplantation research and mobilize knowledge so that every wish to donate is fulfilled and transplantation is transformed from a treatment to a lasting and sustainable cure. The Research Manager holds a key role in national project management of multicenter research studies, with a focus on organ donation and transplantation research. This position involves diverse responsibilities including managing project timelines and deliverables, study wide communication with internal and external stakeholders, supporting Research Ethics Board (REB) submissions and amendments, designing data capture tools, and ensuring the quality and integrity of clinical and laboratory data. Additionally, the Research Manager plays a pivotal role in supporting grant submissions related to projects, and handling various administrative project tasks, such as scheduling meetings with the study team and stakeholders. In this role, the Research Manager is entrusted with ensuring studies adhere to regulations and compliance standards. Reporting to the CDTRP Executive Director, the Research Manager will demonstrate excellent team spirit and a sense of camaraderie.
RESPONSIBILITIES
Under the general supervision of Dr.
Dhanani and the CDTRP Executive Director, the Research Manager will:
- Lead communication across all participating centers in a research study, engaging Principal Investigators, research staff, funding entities, and other healthcare professionals.
- Initiate and facilitate study startup activities, including supporting grant writing, leading ethics submissions, supporting contract negotiations, and staffing.
- Oversee the operations of multiple research facilities, labs, or locations across Canada.
- Establish Master Files for study operations, ensuring all essential documents are up to date,
- Monitor study progress and communications with internal tracking systems, following up with site personnel as needed.
- Perform administrative/managerial tasks in addition to research duties, supporting the Principal Investigators.
- Clearly communicate strategic objectives to study teams, defining shortterm and longterm action plans aligned with these objectives.
- Develop recommendations and action plans to resolve issues affecting study objectives in collaboration with the Executive Director and the Principal Investigators.
- Conduct training for colleagues or study team members, including creating Standard Operating Procedures (SOPs).
- Ensure quality and timely data entry into clinical databases, including reporting and followup of queries, while ensuring compliance with the approved protocol.
- Summarize and organize data for publication, potentially coauthoring or copresenting research papers, presentations, or publications.
- Coordinate with CDTRP leadership, management team, partners, and stakeholders to achieve study objectives, organizing and consolidating progress reports and statements of work.
- Support the study's knowledge mobilization strategy.
Organizational Skills
Teamwork and Communication Skills
Autonomy / Problem Solving
Travel and workspace.
- Will be required to travel to attend national research meetings.
- Bachelor's degree in a life science or other relevant discipline.
- Minimum of 2 years' experience in clinical research.
- Experience working with large cohort studies and clinical trials is an asset.
WORKING CONDITIONS
Will be required to travel to attend meetings (typically twice annually).
OTHER REQUIREMENTS
- Eligible to work in Canada;
- Compliance with CHEO RI's Universal COVID19 Vaccination Policy; and
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