Clinical Research Assistant

2 weeks ago

Toronto, Canada FACET Dermatology Full time

FACET Dermatology is looking for a Clinical Research Assistant to work closely with the clinical research coordinators to assist in study operations. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines.

**Responsibilities**
- Work collaboratively with research team members.
- Maintenance of regulatory documents including the development and upkeep of study binders (electronic/paper).
- Laboratory Processing
- Assist with advance preparation for audits and site visits.
- Check data for accuracy and completeness; score data; enter data, including data re-entry; data cleaning
- Provide support to other research team members, where necessary.
- Assist with site training for site coordinators.
- Develop other study documents as required.
- Participate in study-related meetings
- May involve conducting telephone and/or clinical recruitment interviews
- Coordinating patient visits schedule as per study protocol;
- Executing all aspects of study protocol involving patients visits
- **Qualifications**:_
- Bachelor’s degree, or recognized equivalent, in a health or science-related discipline
- At minimum 2 years clinical research and/or professional experience
- Experience in management of research ethics (REB/HREBA) submissions
- Knowledge of research regulations and guidelines preferred (such as ICH/GCP, Tri-Council Policy, Declaration of Helsinki, and Health Canada TPD (as required)
- Excellent verbal and written communication skills in English
- Intermediate to advanced skills in Microsoft Office, Outlook and basic computer skills
- Excellent organizational and time management skills
- **In order to be successful at this position, you should**:_
- Be a strong team member dedicated to exceptional service, efficiency, and safety.
- Have experience with direct patient care
- Have experience in conducting an informed consent discussion
- Show proficiency in MS Office, Outlook and basic computer skills
- Have experience with the use of electronic case report form (eCRF)
- Be organized, flexible, and willing to step in where needed
- Have attention to detail
- Be self-motivated and a fast learner
- **Preferred requirements**_
- Bachelor’s degree in a health or scientific related program
- A thorough understanding of regulatory requirements
- Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
- Experience with CRIO (Clinical Trial Management System) is a plus
- Experience with administering vaccines is a plus

**Salary**: From $50,000.00 per year

**Benefits**:

- Paid time off

Schedule:

- 8 hour shift
- Monday to Friday

**Education**:

- Bachelor's Degree (required)

**Experience**:

- research: 2 years (required)

Work Location: In person

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