Clinical Research Coordinator - Vancouver, Canada - University of British Columbia
Description
Staff - Non UnionJob Category
M&P - AAPS
Job Profile
AAPS Salaried - Research and Facilitation, Level A
Job Title
Clinical Research Coordinator
Department
Support | Institute for Computing, Information and Cognitive Systems | Faculty of Applied Science
Compensation Range
$4, $6,754.00 CAD Monthly
The Compensation Range is the span between the minimum and maximum base salary for a position.
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Posting End DateApril 19, 2023
Note:
Applications will be accepted until 11:59 PM on the day prior to the Posting End Date above.
Job End Date
Apr 18, 2024
At UBC, we believe that attracting and sustaining a diverse workforce is key to the successful pursuit of excellence in research, innovation, and learning for all faculty, staff and students.
Our commitment to employment equity helps achieve inclusion and fairness, brings rich diversity to UBC as a workplace, and creates the necessary conditions for a rewarding career.
Job SummaryThis position will be responsible for coordinating the activities of the Stillbirth Risk Identification Using Multiparametric Ultrasound (STIMULUS) Study. Funded by Wellcome Leap and led by Dr.
Robert Rohling, [Principal Investigator, Director, Institute of Computing, Information and Cognitive Systems (ICICS), the University of British Columbia (UBC)] STIMULUS aims to reduce stillbirth rates by capturing multiparametric quantitative ultrasound measures of maternal, fetal, and placental function during first, second, and third trimester scans.
Major responsibilities of the position include managing recruitment efforts, database development, oversight of ethics and facilitating communication with team members located at BC Women's Hospital, UBC, and the University of North Carolina at Charlotte.
Organizational Status
This position will report directly to the STIMULUS Clinical Research Manager and is accountable to the Principal Investigator, or his designate, as well as the ICICS Administrator.
Work Performed
- STIMULUS aims to reduce stillbirth rates by capturing multipara metric quantitative ultrasound measures. Sets priorities for study related tasks such as recruitment, database development, oversight of ethics and facilitating communication with team members located at BC Women's Hospital, UBC, and the University of North Carolina at Charlotte.
- Construction, population and maintenance of a participant database; REDCap to organize the data generated from this study.
- Oversees and participates in data collection, analysis and data cleaning as well as preliminary writeup of manuscripts.
- Manages recruitment efforts, including consenting participants, monitoring sample size, and assessing and modifying recruitment strategies where necessary.
- Provides patient education on study background, purpose, procedures and potential benefits and risks.
- Overseeing the preparation and dissemination of program activities; developing content for websites, promotional materials, visual communications, etc.
- Developing, in conjunction with the Director and Research manager, written progress, quarterly, annual and final reports, for projects, grants and collaborations by providing updated budget summary/milestone information.
- Oversees ethics, including the preparation of study amendments and annual renewals, and communicates with the UBC Children's and Women's Research Ethics Board
- Serve as representative at meetings with outside institutions, industry, academia and other research groups as well as with onsite neighbors related to operations issues.
- Records expenditures for Clinical Research Manager's overview
- Facilitates communication with various stakeholders and collaborators at BC Women's Hospital, UBC, and the University of North Carolina at Charlotte.
- Develops standard operating procedures including patient instructions for each study visit, safety and security of ultrasound equipment, etc.
- Performs other related duties as required.
A high degree of accuracy, a thorough understanding of policies and practices, the ability to anticipate, investigate and resolve problems are expected.
The Research Coordinator exercises professional judgment and initiative and is accountable for the effective execution in coordinating the daily activities of (STIMULUS) Study.
Supervision ReceivedWorks independently with limited supervision by Research Manager. Position reports to the ICICS Administrator and STIMULUS Clinical Research
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