Clinical Research Coordinator

1 week ago


Greater Sudbury, Canada Medicor Research Inc Full time

**Position Summary**:
Clinical Research Coordinators, under direction of Investigators/Physicians, manage clinical trials. They are responsible for the organization, patient recruitment, coordination, and overall integrity of a research project.

**Tasks and Competencies**:

- Ensure timely and successful execution of clinical trials
- Coordinate multiple trials simultaneously (volume dependent upon experience) at a variety of physician offices in and around Sudbury
- Serving as the primary contact for assigned studies
- Read, understand and clarify the clinical trial protocols
- Prepare for and attend internal and sponsor meetings
- Ensure all documents to be used for the study fulfill the requirements of GCP-ICH, the protocol, and Medicor policies and procedures
- Ensure all study supplies/equipment have been received and are functioning and of sufficient quantity to begin the study
- Become proficient with procedures and equipment required per protocol
- Ensure training and competency of all study staff correlates with the delegation of tasks by the Principal Investigator (PI); and is maintained throughout the study
- Communicate to the study team as per internal processes
- Coordinate the study as per the most recent version of the approved protocol within GCP-ICH and Medicor policies and procedures.
- Prepare lab and diagnostic, adverse events, and study documents for PI review and signature in a timely manner.
- Manage data and data entry as per GCP-ICH, sponsor and Medicor guidelines
- Prepare for monitoring visits and allocate time to meet with the Monitor daily while they are on-site
- Make certain the study is audit ready at all times

**Preferred Education**:

- At minimum, a Bachelor’s degree in science or related field.
- Job specific training provided under extensive internal training program (both theory and practical training)

**Knowledge and Skills Required**:

- Bring high level of professionalism, energy and passion
- Excellent interpersonal and communication skills
- Proficiency with Outlook, Word, Power Point and Excel
- Strong organizational and time management skills
- Strong analytical and problem solving skills
- Ability to work independently as well as part of a team; self-motivated
- Excellent written and verbal communication skills

**Benefits**: available after 3 month probationary period

**Status**: full-time, permanent

**Salary Range**:$25 to $36 (hourly)

**Reporting to**: Clinical Team Manager

**Other requirements**
- Valid G class driver’s license
- Access to vehicle during business hours
- Vaccines (COVID and others)
- Beneficial - valid passport

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

**Salary**: $25.00-$36.00 per hour

**Benefits**:

- Dental care
- Extended health care
- On-site parking
- Paid time off
- Vision care

Schedule:

- Monday to Friday

**Education**:

- Bachelor's Degree (preferred)

Work Location: In person

Application deadline: 2023-12-07



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