Clinical Research Associate at 410 ICR United States USA

What You Will Do:Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders.Key responsibilities include:Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentationRunning 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 maintalaborative relationships with key stakeholders, clinical investigators, and site staff.Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.Your Profile:You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.Required qualifications and experience:University degree ence, or equivalentKnowledge of ICH-GCP guidelines and the expertise to review and evaluate medical dataExcellent written and verbal communication in EnglishGood social skills enabling you to deal with queries in a timely mannerWillingness to travel as required (approximately 60%)Employment with ICON is contingent upon having the legal right to work in the country where the role is based.Rewards & BenefitsICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.Benefits may include:Competitive base salary and performance related incentivesHealth and wellbeing programmes including medical, dental, and vision coverage where applicableRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysBenefits may vary depending on role and location.Visit our careers site to read more about the benefits ICON offers.Inclusion and AccessibilityICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Clinical Research Associate

Emma

Responsibilities

Skills wanted:

Language(s) required:

Admin access needed