Senior Clinical Research Associate coordinating activities for clinical trials at ICON. Working independently to ensure accurate study documentation and protocol submissions.
Responsibilities
Coordinate activities to set up and monitor a study
Complete accurate study status reports and maintain study documentation
Submission of protocol, consent documents for ethics/IRB approval
Assist in preparing regulatory submissions as requested
Participate in preparing and reviewing study documentation and feasibility studies for new proposals
Balance sponsor generated queries efficiently and responsible for study cost-effectiveness
Assist in training and mentoring less expert CRA's and/or lead CRA's working on international projects
Requirements
18 months+ of monitoring experience in phase I-III trials as a CRA
Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
Excellent written and verbal communication in English
Ability to produce accurate work to tight deadlines within a pressurized environment
Valid driving license and willingness to travel at least 60% of the time (international and domestic).
Benefits
Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
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