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.
Online Brand Protection Analysts combating online infringement by identifying unauthorized uses of intellectual property. Collaborating with teams to ensure brands are safeguarded and protected efficiently.
Market Research Analyst Intern involved in market research and marketing strategy for BD. Collaborating with teams to analyze trends and support product development projects.
Aurora Energy Research looking for recent graduates to enhance clients’ decision making through rigorous analysis. Contribute to product development and client engagement in a dynamic environment.
Research Analyst engaging in energy sector decision - making and client insights. Collaborating with teams to deliver quantitative analyses in a dynamic environment.
Research Associate at the University of Alberta overseeing the 3MDR program management. Responsible for project design, execution and collaboration with research investigators.
Data Entry Specialist managing data entry tasks at Credibly. Using computers effectively to enter data while ensuring accuracy and meeting production levels.
Senior Clinical Research Associate managing local study delivery and site monitoring for clinical studies. Collaborating with various stakeholders in accordance with clinical guidelines and local regulations.
Senior Clinical Research Associate responsible for monitoring and managing clinical studies at various local sites. Collaborating with various stakeholders to ensure timely study conduct and compliance with international guidelines.
Research Associate at Surgo Health ensuring the quality of large - scale survey data for healthcare analytics. Join a team committed to advancing healthcare insights through data - driven solutions.
Research Specialist supporting the IHOPE study and conducting clinical visits at Emory University. Collaborating with Dr. Abigail Lott and maintaining laboratory records in Atlanta, Georgia.