Note: The job is a remote job and is open to candidates in USA. ICON Strategic Solutions is hiring a Clinical Research Associate I to support clinical trial operations in a sponsor-dedicated model. The role involves coordinating study setup and monitoring, maintaining study documentation, collaborating with stakeholders and site staff, and ensuring patient safety and regulatory compliance.
Responsibilities
- Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
- Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required
- Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
- Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements
Skills
- Relevant clinical trial monitoring experience
- University degree in medicine, science, or equivalent
- Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
- Excellent written and verbal communication in English
- Good social skills enabling you to deal with queries in a timely manner
- Legal right to work in the country where the role is based
Benefits
- Performance related incentives
- Medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
- Remote work
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