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 investigative sites or through remote methods.

• Guarantee that clinical trials are carried out, documented, and reported in accordance with the established protocol.

• Ensure adherence to standard operating procedures (SOPs), ICH-GCP guidelines, and relevant regulatory standards.

• Provide support for clinical research initiatives in pharmaceutical, biotechnology, medical device, government, and public health sectors.

⛳️ Requirements

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

• A minimum of 1 year of clinical monitoring experience or an equivalent combination of education and experience necessary for the level 2 position.

• At least 3 years of clinical monitoring experience required for a level 3 position.

• Experience in oncology monitoring is preferred.

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

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

• Must be legally authorized to work in the United States or Canada.

• Must not require, either now or in the future, sponsorship for employment visa status.

• Bilingual proficiency in English and French is required.

🏝️ Benefits

• Competitive base salary.

• Incentives related to performance.

• Medical, dental, and vision insurance where applicable.

• Retirement and pension plans.

• Coverage for life assurance and disability.

• Employee assistance programs and wellbeing resources.

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

• Supportive policies and wellbeing initiatives.

• Reasonable accommodations during the recruitment process.