Clinical Research Assistant

1 week ago

Edmonton, Canada VIDA Dermatology Full time

**Our Company**

VIDA Dermatology is Edmonton's state-of-the-art Dermatology clinic in south Edmonton. We are a comprehensive dermatology clinic and provide solutions for medical, surgical and cosmetic treatments to all patients and age groups.

**PURPOSE**

**Job description - Research Assistant/Backup to Research Coordinator**

**Responsibilities**

Possess high-level working knowledge and understanding of all assigned protocols, including requirements of patient eligibility, meeting enrollment goals, visit schedule, assessments and lab procedures, drug accountability, and maintenance of regulatory documents.

Other responsibilities include patient recruitment, scheduling patient visits according to protocol schedule, reporting protocol deviations and gathering information on AEs and SAEs and reporting to physician, supervisor, and Sponsors as required per protocol. Medical history and concomitant medication history collection by patient interview and taking vital sign measurements.

Qualifications:

- Bachelors degree minimum, Masters degree preferred with a strong academic record. RN or RPN with experience in Clinical Research is preferred.
- Minimum of two full years of clinical research assistant experience
- Experience in management of research ethics (REB/HREBA) submissions
- Must be able to work independently and efficiently; multi-task and be organized and be highly detail-oriented.
- Experience with Phlebotomy, Laboratory sample processing and ECG collection is an asset
- Study Drug administration experience (topical and sub-cutaneous injection)
- Excellent organizational and time management skills
- Conduct site qualification, initiation, monitoring, and closeout visits for clinical trials
- Ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines
- Collect and review study data, ensuring accuracy and completeness
- Monitor participant safety and report adverse events to the appropriate parties
- Maintain study documentation and files in accordance with regulatory standards
- Collaborate with cross-functional teams to ensure timely completion of study milestones
- Assist in the development and review of study protocols and informed consent forms

'''Skills''':

- Proficiency in SAS, Python, and R for data analysis and reporting
- Strong understanding of clinical research processes and regulations
- Excellent attention to detail and organizational skills
- Effective communication and interpersonal skills for collaboration with study teams
- Ability to work independently and manage multiple tasks simultaneously
- Problem-solving skills to address challenges that may arise during the course of a study

Note: Additional qualifications or specific requirements may vary depending on the organization or project.

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

Pay: $23.00-$28.00 per hour

Expected hours: 41.5 per week

**Benefits**:

- Company events
- Dental care
- Employee assistance program
- Extended health care
- On-site parking
- Paid time off
- Store discount
- Wellness program

Flexible language requirement:

- French not required

Schedule:

- 8 hour shift
- Monday to Friday
- Weekends as needed

Work Location: In person

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