Clinical Research Associate
ICON plc is a world‐leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Role Details
Role: Clinical Research Associate (CRO and/or Pharma monitoring and Oncology experience required)
Location: Must be based in the UK, nationwide travel
Fully sponsor dedicated
Responsibilities
* Conducts site selection for potential sites to evaluate their capabilities for conducting a clinical trial. Recommends sites to participate in clinical trial. Is the frontline liaison between ICON and sites to ensure successful collaboration, meeting ICON expectation on milestone and deliveries.
* Manages assigned study sites and networks, if applicable, conducting phase I-IV protocols according to the monitoring plan and our clients procedures. Performs Site Initiation Visit, ensures site personnel is fully trained on all trial related aspects. Performs continuous training for amendments and new site personnel as required. Retrains site personnel as appropriate.
* Conducts continuous monitoring activities (onsite and remote). Implements site management activities to ensure compliance with protocol, GCP, global and local regulations, global and local processes to secure data integrity and patient safety. Is accountable for continuously updating all electronic systems (global and local) relevant to perform job functions.
* Ensures that study milestones for sites responsible are met as planned (i.e., study startup, recruitment, database analyses, closeout, etc.). Performs Site Closeout activities per SOPs and applicable regulations to ensure that site is aware of any follow up activity and archiving requirements. Attends onboarding, disease indication and project specific training and general CRA training as required.
* Documents monitoring activities appropriately following ICON standards. Collaborates with the CRA Group Head/CSM to ensure recruitment plans and execute contingency plans, as needed. Participates from audit organization and inspection readiness activities for monitoring and site related activities as required and ensures implementation of corrective actions within specified timelines.
* Performs additional task as assigned Delivery of quality data and compliance to quality standards.
* Monitors studies as per current legislations, ICH/GCP and our clients standards. Ensures timely delivery, of high quality, robust and reliable data of the monitored sites to support the goals of Trial Monitoring as defined by Trial Monitoring. (ADIS, DBL). Identifies issues at sites; resolves issues and escalates as appropriate.
* Collaborates with internal stakeholders and site personnel to manage data query resolution process to ensure timely and accurate data entry. Ensures the site Investigator Folder is up to date. Is responsible for collecting essential documents from site and accountable to keep sTMF(s) current. Supports the implementation of innovative processes and technologies Budget and productivity.
* Negotiates investigator remuneration; prepares financial contracts between ICON and investigational sites and investigators. Ensures that payments are appropriately triggered to investigational sites.
Qualifications
* Right to work in the UK.
* Up to 2 years pharmaceutical/CRO industry experience.
* Good knowledge of drug development process specifically clinical trial/research.
* Knowledge of international standards (GCP/ICH, FDA, EMEA).
* 12+ months' monitoring experience required.
Additional Requirements
* Ability to travel domestically (and possibly internationally) as needed to study sites and for training and meetings.
* A minimum of 50% overnight travel may be required.
What ICON can offer you
In addition to a competitive salary, ICON offers a range of additional benefits designed to be competitive within each country and focused on well‐being and work‐life balance opportunities for you and your family.
Benefits examples include:
* Various annual leave entitlements.
* A range of health insurance offerings to suit you and your family's needs.
* Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead.
* Global Employee Assistance Programme, TELUS Health (LifeWorks), offering 24‐hour access to a global network of over 80,000 independent specialised professionals 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.
Equal Opportunity
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
Apply
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there's every chance you're exactly what we're looking for at ICON.
Visit our careers site to read more about the benefits ICON offers.
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