Overview
Research Assistant Jobs in Edmonton, AB at Prime Site Research Solutions Inc
Full job description
Closing date:Will remain open until suitable candidate found
Salary:Commensurate with experience
Benefits:Health/dental plan, employee & family assistance program, retirement plan, perks
Start Date:Jun/Jul 2024
Primesite Research Solutions is an Integrative Research Organization and Site Network based out of Western Canada. We conduct phase I, II, III, IV clinical trials in various clinical areas at local hospitals and clinics. We are seeking a research assistant to join our growing site network. This position requires a self-motivated, organized, and accountable individual with strong attention to detail. The applicant must have the ability to prioritize and multi-task in a complex rapidly changing environment and must be able to promote teamwork, collaboration, and problem-solving skills. In this position the research assistant will work under the supervision of the research coordinators and research manager to fulfill clinical trials related responsibilities and ensure that each study progresses efficiently. The research assistant will also be responsible for data entry and management of selected patient registries. This position requires frequent contact with physicians, other staff, study participants, biopharma companies and regulatory agencies, and has significant potential for advancement.
Key Responsibilities:
Adhere to multiple research protocols, confidentiality, ICH, GCP & NIH guidelines
Prepare REB submissions and other regulatory documents required for study initiation
Perform data entry for clinical trials and registries
Prepare for and participate in monitoring visits and conference calls
Develop study files in accordance with various protocols
Provide administrative support including filing, directing phone calls, updating tracking logs and maintaining trial regulatory documents
Organize and maintain project/task management system and clinical trials management system (CTMS)
Organize, prioritize and respond appropriately to incoming correspondence
Maintain optimal office systems, processes and equipment
Coordinate with various departments and correspond with study sponsors and regulatory agencies
Communicate study procedures and provide ongoing support to staff
Screen hospital charts for potential study participants and be able to discuss eligibility with coordinators and physicians
Organize ongoing patient follow up and study visits
Perform study procedures (including collection of vital signs, blood, ECGs etc) as requested
Comfortable handling and transporting blood, marrow and other lab samples
Travel between hospitals for various tasks
Work effectively with study research coordinators and manager to ensure open communication and efficient prioritization of all assigned responsibilities
Required Skills for Success:
Undergraduate degree required, patient interaction and clinical trials experience are preferred (other education with clinical research experience will be considered)
2-3 years of experience in working with clinical trials/research studies
Must be comfortable interacting directly with patients
Working knowledge of Microsoft Office software (Word and Excel) and Google Apps (Docs and Sheets) required
Tech savvy, willingness to learn and adapt to new technologies, and ability to proficiently use required technologies and applications: online software including for meetings, training, timeshe…
Title: Research Assistant
Company: Prime Site Research Solutions Inc
Location: Edmonton, AB
Category:
