Job Description

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

Our facility is looking to add a

Clinical Research Assistant

to our beautiful clinic located in South Edmonton. The ideal candidate for this role is self-motivated and has a strong interest in the Dermatology field and experience in this role. The position will serve as

Backup/Assistant to Research Coordinator

Job description - Research Assistant/Backup to Research Coordinator

Responsibilities

The successful candidate will work under the direction of Principal Investigator and as part of the Clinical Research Team to assist in research study operations.

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.

Experience reviewing and conducting Informed Consent process with subjects, creating source documentation when required and completing all study specific documents within the specified timeline. Review, file, and respond to all study specific documents, correspondence, and requests.

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 asset, 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

We thank all applicants for their interest but only candidates selected for an interview will be contacted.

Duties:

- 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.

This position offers an exciting opportunity to contribute to cutting-edge clinical research projects. As a Clinical Research Associate, you will play a crucial role in ensuring the successful execution of clinical trials. You will collaborate with cross-functional teams, collect and analyze data, monitor participant safety, and maintain regulatory compliance. Proficiency in SAS, Python, and R is essential for this role to perform data analysis and reporting. Strong attention to detail, organizational skills, and effective communication are also key attributes for success in this position. If you are passionate about clinical research and have the necessary skills, we invite you to apply for this rewarding opportunity.

Job Types: Full-time, Permanent

Pay: $21.00-$28.00 per hour

Benefits:

Dental care Extended health care On-site parking Paid time off Store discount Wellness program
Work Location: In person