Clinical Research Coordinator III (PK)

University Health Network • Toronto, ON

8d • CA$84,779 - CA$105,968 • Onsite

About The Position

The Clinical Research Coordinator collaborates with Investigators and health care team to assume responsibility for the overall patient management and coordination of several clinical studies for the Drug Development Program at Princess Margaret Cancer Centre. Studies include pharma-sponsored, cooperative group sponsored (such as NCIC) as well as Investigator initiated trials.

Requirements

• Bachelor’s degree, or recognized equivalent, and current certificate of competence (licensure/registration) from a college legislated under the Regulated Health Professions Act, required
• Registered Nurse with a minimum of 3 (three) years experience.
• Excellent phlebotomy, IV and CVL skills
• Minimum one (3) year clinical experience in oncology with strong knowledge base
• Strong analytical and problem solving skills
• Excellent interpersonal, verbal and written communication skills required
• Ability to set priorities and work independently with accuracy in a dynamic environment
• Proficiency with MS Office software - Word and Excel desired.

Nice To Haves

• CNA certification in Oncology preferred
• deSouza Chemo/Bio certification preferred
• Recognized certification in clinical research (ACRP or SOCRA) obtained or plans to work towards.
• Knowledge of IATA shipping regulations and basic laboratory procedures an asset
• Previous clinical research experience preferred
• Training in ICH/GCP guidelines an asset.
• Demonstrated knowledge and ability to utilize the nursing process in planning, implementing and evaluating patient care
• Evidence of good physical assessment, psychosocial assessment and patient/family teaching skill
• Autonomous clinical critical thinking ability
• Excellent organizational and time management skills required

Responsibilities

• Coordination of patient activities such as sample collection including processing and shipment of samples according to clinical trials protocols
• Assessments, vital signs, ECG’s, monitoring and administration of treatments as per study protocol
• Assists the primary Clinical Research Coordinator III with clinical care for patients participating in clinical trials and the implementation and coordination of all aspects of data collection and source documentation, as per UHN policy and ICH/GCP guidelines

Benefits

• Competitive offer packages
• Government organization and a member of the Healthcare of Ontario Pension Plan (HOOPP)
• Close access to Transit and UHN shuttle service
• A flexible work environment
• Opportunities for development and promotions within a large organization
• Additional perks (multiple corporate discounts including: travel, restaurants, parking, phone plans, auto insurance discounts, on-site gyms, etc.)

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level