Clinical Research Coordinator (Internal Med/Alberta)

Position Description

Coordinates daily operations of clinical research studies in assigned department(s). This includes but is not limited to overall clinic conduct, marketing, and data management of all clinical research activities in assigned department(s). Carries out supervisory responsibilities in accordance with policies and applicable laws. Responsibilities may include training new employees; assisting with planning, assigning, and directing work; addressing complaints and resolving problems. The employee is frequently exposed to fumes or airborne particles. The employee is occasionally exposed to toxic or caustic chemicals and dangerous bodily fluids. The noise level in the work environment is usually moderate. Approximately 5-15% travel (often long-distance) is required.

Preferred Qualifications

• Bilingual Spanish/English

• Current certification as a Clinical Research Coordinator

• Experience in oncology nursing

• Experience working with clinical (pharmaceutical) research trials

• Experience working with IRB

• Experience in the peer review research publication process

Required Qualifications

• Healthcare related training with current licensure/certification in their field OR

• Bachelor's degree from an accredited university with a major in the area of research being conducted.

• Certified Clinical Research Professional as defined by The Society of Clinical Research Associates or Certified Clinical Research Coordinator as defined by the Association of Clinical Research Professionals OR

• Ability to obtain certification as a Clinical Research Professional/Coordinator within two years from date of hire or upon eligibility.