Clinical Research Coordinator - Edmonton, Canada - University of Alberta

University of Alberta

Verified Company

Edmonton, Canada

1 week ago

Posted by:

Sophia Lee

beBee Recruiter

Description

MED Obstetrics And Gynaecology:

Competition No.

Posting Date

Feb 14, 2024

Closing Date

Feb 22, 2024

Position Type

Part Time - Grant Funded

Salary Range

$25,910 to $35,191 (pro-rated) per year

Grade

Hours

17.5
This position is a part of the Non-Academic Staff Association (NASA).

This position has a term length of 1 year plus a day and offers a comprehensive benefits package which can be viewed on our Benefits Overview page.

Location - Work primarily takes place at North Campus Edmonton.

Working for the University of Alberta

The University of Alberta acknowledges that we are located on Treaty 6 territory, and respects the histories, languages and cultures of First Nations, Métis, Inuit and all First Peoples of Canada, whose presence continues to enrich our vibrant community._

The University of Alberta is teeming with change makers, community builders, and world shapers who lead with purpose each and every day.

We are home to more than 40,000 students in 200+ undergraduate and 500+ graduate programs, over 13,000 faculty and staff, 260,000 alumni worldwide and have been recognized as one of Canada's Greenest Employers for over a decade.

Your work will have a meaningful influence on a fascinating cross section of people—from our students and stakeholders, to our renowned researchers and innovators who are quite literally curing diseases, making discoveries and generating solutions that make the world healthier, safer, stronger, and more just.

Working for the Department
This position is located at the Royal Alexandra Hospital.

The Department of Obstetrics and Gynecology has five academic divisions, 19 full-time academic faculty members, and over 100 clinical academic colleagues in general obstetrics and gynecology.

Our faculty members encompass the full range of academic medicine including Maternal-Fetal Medicine, Reproductive Endocrinology & Infertility, Gynecological Oncology, Reproductive Sciences and Urogynecology.

This accomplished team of educators trains medical undergraduate and postgraduate students in the provision of innovative patient care.

Our passion for delivering the highest quality education is matched by our research strength. Multidisciplinary and collaborative research projects are nurtured and developed across disciplines, departments and faculties.

The department's distinguished cadre of scientists focus on clinical, discovery and translational research that bring our work from the lab bench to the bedside, where it matters most.

Position

The Clinical Research Coordinator is responsible for supporting multiple clinical and basic science research studies in the area of perinatal and/or women's health, at the Lois Hole Hospital for Women (LHHW) and the University of Alberta.

The position works within the research support platforms team in Obstetrics & Gynecology in collaboration with the Women and Children's Health Research Institute (WCHRI) and reports to the Research Team Lead in OBGYN.

The Clinical Research Coordinator works collaboratively with investigators, study participants, health care providers, and other research support staff in order to ensure safe and successful conduct of clinical, basic science and translational research studies.

The position provides direct support for biological sample collection for investigators in the Division of Reproductive Sciences in the Department of Obstetrics & Gynecology and their collaborators.

The position may provide a range of research support services, including (but not limited to) contract and ethics submissions; study setup, conduct, and closeout.

Duties
Protocol Management (50%)

Assists in the development and feasibility assessment of clinical research protocols.
Under mínimal supervision, reviews, becomes knowledgeable about, and adheres to multiple research protocols.
Develops excellent studyspecific source documents and precise documentation of same.
Organizes and prepares charts; case report forms; remote data entry for study visits; regulatory documents.
Documents appropriately in electronic medical records (Connect Care).
Conducts the daily aspects of clinical trials according to defined study protocols.
Conducts testing according to specific study requirements.
Coordinates with radiology, laboratory, pharmacy, health records, etc. as needed by specific protocols.
Reports adverse events promptly to the Principal Investigator(s) and the sponsor, as necessary.
Participates in studyrelated meetings, such as principal investigator meetings, site visits, regular monitoring visits and study conference calls.
Ensures source documents are received and reviewed (for example: ECGs, lab work, hospital diagnostic tests).
Enter study information into the ethics system, including annual renewals and amendments. Submit safety reports to Ethics as applicable.
Facilitates closeout of projects.
Assists with g