Clinical Trial Assistant
6 months ago
**Clinical Trial Assistant - Job Description**
**Job Summary**
AvantDerm is seeking an experienced Clinical Trial Assistant (CTA) who will provide support to the clinical research team. As a CTA you will assist the Principal Investigator and Clinical Research Coordinator with the daily tasks involved in conducting clinical trials. You will be responsible for performing administrative tasks, coordinating activities, and maintaining study documents.
**You will provide support in the following tasks**:
- Coordinate clinical research activities, including protocol reviews, IRB and applicable
- Discuss study protocols with patients and verify the informed consent documentation
- Communicate details of participation with patients and meet with patient for each visit
and maintain accessibility to discuss any questions/concerns regarding the study
- Handle biological specimens (IATA certificate required)
- Perform ECGs and obtain vital signs of patients
- Collect blood samples, centrifuge and ship samples
- Cross coverage in the clinic supporting other administrative tasks and duties
- Schedule all patient research visits and procedures consistent with protocol
requirements
**Here’s What You’ll Need**:
**Essential Requirements**
- Strong clinical research experience (Dermatology experience is an asset)
- Genuine desire to work in a dynamic, fast-paced environment
- Excellent verbal and written skills, great at explaining complex concepts
- A high degree of autonomy and reliability; very detail oriented
- A go-getter attitude, you take accountability for your work
- Extremely organized and efficient
- Assist with recruitment of study participants (e.g. database search, screening potential
participants and obtaining informed consent form)
- Other administrative duties as needed
- Team player
**Assets**:
- Knowledge of ICH/GCP guidelines (must have updated GCP training certificate, Division
5, and E6 Revision 2)
- Experience with handling biological specimens (IATA certificate required)
- Maintenance of SOPS, temperature logs, and site logs
- Proficiency with computers, Microsoft Office, Google Workspace, databases and EMR
- Bachelor’s Degree: Science, Health Science, psychology, RN/RPN
- Phlebotomy experience is a strong asset
- Certification as a Clinical Research Professional or eligibility to obtain certification
**Salary**: $20.00-$22.00 per hour
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Application question(s):
- Do you have any phlebotomy experience?
**Education**:
- Bachelor's Degree (preferred)
**Experience**:
- clinical research: 1 year (preferred)
Ability to Commute:
- Toronto, ON (required)
Work Location: In person
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