Research Advisor - Montréal, Canada - McGill University

McGill University
McGill University
Verified Company
Montréal, Canada

1 week ago

Sophia Lee

Posted by:

Sophia Lee

beBee Recruiter
Description
Please refer to the

job aid for instructions on how to apply.


Primary Responsibilities:

  • Facilitate, coordinate, enhance and promote McGill's research and development activities by coordinating and administering clinical trial projects at the Clinical Research Unit at the MNI.
  • Oversee and is responsible for all out of province patient contacts (within Canada or International).
  • Work alongside Medical Director and Principle Investigator to advise and inform external patients on clinical trial opportunities and appropriate Clinical Research sites globally.
  • Provide guidance and information on clinical trial options to participants and advise on which clinical trial site is most appropriate according to their situation
  • Interpret information received on patients and determine the most appropriate procedures and trials for performing the research and ethics administration activities. Responsible of ensuring that the activities are performed in accordance with each individual clinical trial protocol and University and sponsors policies and procedures.
  • Liaise and communicate information to medical staff, patients and pharmaceutical companies on new information pertaining to patients, changes to regimens, deadlines in terms of tests to be performed (i.e., CT scan, blood tests, etc), regulatory information, etc.
  • Educate patients, researchers and nurses to follow protocol according to GCP guidelines.
  • Act as the primary liaison between researcher, patient and pharmaceutical company. Attends all internal and external meetings as requested by the medical director and/or the pharmaceutical company for each clinical trial the coordinator is responsible for.
  • Establish compliance with internal, sponsor, and regulatory requirements, set internal policies and procedures for ALS & Neuromuscular team on correspondences and documentation for sponsors and CROs.
  • Functions as a recordkeeper and document patient information pertaining to the study and organize and lead the followup of business.
  • Resolves any equipment issues and supports with the functional assessments pertaining to the study equipment (smart devices, ECG and any other sponsorprovided tools): organize proper calibration with equipment expert, alert provider of any defects/issues in performance, ensure inventory for ancillary/disposable supplies, etc.
  • Train and act as a resource for new research administrators on the ALS and neuromuscular team and support training on other teams as needed.
  • Train staff members and study personnel on GCP, SOPs, Division 5, proper study documentation, sponsor and regulatory requirements.
  • Responsible for overseeing and triaging all new participants and assigning them to the most appropriate research coordinator
  • Lead all participant recruitment initiatives on the ALS team
  • Perform other administrative duties as required.
  • Minimum Education and Experience:
  • Bachelor's Degree 3 Years Related Experience /

Annual Salary:
(MPEX Grade 05) $65, $81, $98,240.00

  • Hours per Week:
Full time)

Supervisor:
Manager CRU

Position End Date (If applicable):

  • Deadline to Apply:
- ._
More jobs from McGill University
See all jobs of McGill University