Clinical Research Coordinator

Job Description: Clinical Research Coordinator

**C-health, a WELL Health Company, is committed to provide patients with excellent comprehensive care, and is comprised of a network of collaborative multi-specialty teams. Our specialist clinics are co-located to enhance support for physicians and the quality of care for patients. This is a fast-paced, highly collegial, and professional environment that takes immense pride in the patient-centric care that is delivered. At C-health our team of medical specialists and allied healthcare professionals work together to offer the best integrative care to each and every patient.**

We are seeking a dynamic **Clinical Research Coordinator**to assist in conducting clinical trials.

**Why join C-health (a WELL Health Company)? Here are a few great reasons**:

- Largest community endocrinology care provider in Alberta
- Largest providers of cardiovascular care in Calgary
- Work with top experienced research personnel
- Work with Multi-Specialty and Multidisciplinary teams
- High standards of operating procedures
- 45000+ Albertans cared for by C-health

**Responsibilities**:

- **Clinical Research**_
- Participates in study related meetings such as site evaluations, site initiations, close-out visits, investigator meetings, monitor visits and study conference calls.
- Adheres to Standard Operating Procedures (SOPs), Internal conference of Harmonization (ICH), Good Clinical Practice (GCP), and Tri-Counsel Policy Statement: Ethical Conduct for Research Involving Humans, (TCPs) and other applicable regulator requirements.
- Prepares HREBA submissions, including informed consents.
- Act as liaison between investigators, primary care providers and the sponsor
- Responsible for all data and source documentation, serious adverse event and adverse experience reporting, and maintenance of regulatory files along with any other study related duties assigned
- Participates in development and maintenance of quality control and assurance program

**Qualifications**:

- 1 - 3 years previous research and research administrative experience preferred
- Training in clinical trials
- Excellent interpersonal and communication skills, attention to detail, precise documentation skills and time management.
- Proven ability to strategize, plan and coordinate multiple trials and projects
- Experience in laboratory/medical environment
- Experience in Electronic Medical Records
- Ability to liaise effectively with a variety of internal and external research stakeholders

**Personal**:
Have a cheerful, positive attitude and the ability to work effectively with others as well as the ability to work independently and treat everyone with respect, dignity and kindness.
- **C-health offers an excellent remuneration package including competitive wages, medical and dental benefits, training & development assistance, various corporate discounts, unique benefits, and referral bonuses.**_

**Job Types**: Part-time, Permanent

Expected hours: 24 per week

Additional pay:

- Overtime pay

**Benefits**:

- Company events
- Dental care
- Extended health care
- Life insurance
- On-site parking
- Vision care

Schedule:

- 8 hour shift
- Day shift
- Monday to Friday
- No weekends
- Overtime

Ability to commute/relocate:

- Edmonton, AB T6H 4K1: reliably commute or plan to relocate before starting work (preferred)

**Education**:

- Secondary School (preferred)

**Experience**:

- Clinical Research: 1 year (preferred)

**Location**:

- Edmonton, AB T6H 4K1 (preferred)

Willingness to travel:

- 25% (preferred)

Work Location: In person