Senior Clinical Research Associate

📋 Description

• Conduct independent and proactive work to establish and oversee studies, generate reports, and maintain comprehensive documentation.

• Submit protocols and consent documents for ethics/IRB approval, along with preparing regulatory submissions.

• Manage and balance queries generated by sponsors.

• Take responsibility for ensuring cost efficiency in studies.

• Prepare and review study documentation and feasibility assessments for new proposals.

• Opportunity to assist in the training and mentoring of fellow Clinical Research Associates (CRAs).

⛳️ Requirements

• A minimum of 18 months of monitoring experience in phase I-III trials as a CRA.

• A college degree in medicine, science, or a related field.

• Prior monitoring experience in medium-sized studies, including study initiation and closure.

• Familiarity with ICH-GCP guidelines and the ability to review and assess medical data.

• Exceptional written and verbal communication skills.

• Ability to meet tight deadlines.

• Willingness to travel at least 60% of the time (both international and domestic) and possess a valid driving license.

🏝️ Benefits

• Various annual leave entitlements.

• A selection of health insurance options tailored to meet the needs of you and your family.

• Competitive retirement planning solutions designed to maximize savings and help you plan confidently for the future.

• Access to a Global Employee Assistance Programme, TELUS Health, providing 24-hour support from a network of over 80,000 independent specialized professionals to assist you and your family's well-being.

• Life assurance coverage.

• Flexible, country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, and more.