Senior Clinical Research Associate

This is a fully remote position, open to applicants in Canada, +1 more country.

📋 Description

• Oversee the advancement of clinical studies at research sites or from a remote location.

• Ensure that clinical trials are executed, documented, and reported in accordance with the protocol, SOPs, ICH-GCP, and relevant regulatory standards.

• Provide assistance for clinical research across pharmaceutical, biotechnology, medical device, government, and public health sectors.

• Willingness to travel up to 70% of the time.

⛳️ Requirements

• A bachelor's degree or its international equivalent in a scientific or health-related discipline, or a comparable combination of education and clinical research experience.

• At least 1 year of clinical monitoring experience or a suitable combination of education and experience for the level 2 position.

• Minimum of 3 years of clinical monitoring experience for a level 3 position.

• Preferably possess oncology monitoring experience.

• Must be able to travel 70% of the time.

• Familiarity with ICH and local regulatory authority regulations concerning drug trials.

• Legally permitted to work in the United States or Canada.

• Must not need, now or in the future, sponsorship for visa status regarding employment.

• Bilingual proficiency in English and French is required.

🏝️ Benefits

• Competitive base salary along with performance-based incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans available.

• Life insurance and disability coverage provided.

• Employee assistance programs and wellness resources offered.

• Opportunities for learning and development through structured training and career progression.

• Supportive policies and wellness initiatives in place.

• Reasonable accommodations during the recruitment process are available.