Jasper Alberta Clinical Research Associate

The Fairmont Jasper Park Lodge; Municipality of Jasper; Hybrid; CAD 70,000 - 90,000; Full time

Job summary

A hospitality company in Jasper, Alberta is seeking a dedicated Clinical Research Associate. The role involves monitoring clinical trials, ensuring compliance with regulations, and collaborating with stakeholders. Candidates should have a Bachelor's degree and at least 2 years of experience in clinical research, with a preference for oncology and infectious disease backgrounds. This full-time position offers remote flexibility and excellent benefits including health care and paid time off.

Benefits

Dental care

Extended health care

Paid time off

Qualifications

• 2 years of experience as a Clinical Research Associate.
• Experience in Oncology and Infectious Disease preferred.
• Ability to work independently and collaboratively.

Responsibilities

• Monitor clinical trial sites for adherence to protocols.
• Conduct site visits and perform data verification.
• Collaborate with investigators to address trial issues.
• Prepare and maintain study documentation.
• Analyze data using statistical software.
• Provide training to site personnel.

Skills

Analytical skills

Communication skills

Attention to detail

Statistical programming (SPSS, SAS)

Education

Bachelor’s degree in life sciences or related

Tools

SPSS

SAS

Job description

Jasper Alberta Clinical Research Associate

Overview

We are seeking a dedicated and detail-oriented Clinical Research Associate to join our dynamic team. In this role, you will be responsible for overseeing clinical trials and ensuring compliance with regulatory requirements. You will work closely with various stakeholders, including clinical sites, sponsors, and regulatory bodies, to facilitate the successful execution of research studies.

Responsibilities

• Monitor clinical trial sites to ensure adherence to study protocols and regulatory guidelines.
• Conduct site visits and perform data verification to ensure accuracy and integrity of clinical data.
• Collaborate with investigators and site staff to address any issues that arise during the trial.
• Prepare and maintain study documentation, including case report forms and regulatory submissions.
• Analyze data using statistical software such as SPSS, or SAS to support research findings.
• Perform data review and resolution of queries to maintain high-quality clinical data.
• Provide training and support to site personnel on study procedures and compliance requirements.

Qualifications

• Bachelor’s degree in a relevant field such as life sciences, nursing, or a related discipline.
• Minimum of 2 years of experience as a Clinical Research Associate.
• Candidates with experience in Oncology and Infectious Disease will be given preference.
• Proficiency in statistical programming languages such as SPSS or SAS is highly desirable.
• Strong analytical skills with attention to detail and accuracy.
• Excellent communication skills, both verbal and written.
• Ability to work independently as well as collaboratively within a team environment.
• Strong organizational skills with the ability to manage multiple tasks effectively.

Job Details

• Job Type: Full-time
• Location: Alberta (Remote)
• Expected hours: 40 per week
• Benefits: Dental care, Extended health care, Paid time off
• Education: Bachelor's Degree (required)
• Experience: Clinical Research Associate: 2 years (preferred)