Clinical Research Associate

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. We are currently recruiting for an experienced Clinical Research Associates in Romania to work on diabetes, obesity, and rare blood and endocrinology studies. This particular CRA role is a client dedicated one where you will work exclusively on one sponsors trials and SOPs; you will work for a client that values their staff and puts an emphasis on career development.

What You Will Be DoingThe CRA is responsible for the initiation, monitoring and closure of assigned sites in clinical studies, in compliance with sponsor's procedural documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies. Primary point of contact between site staff and the sponsor. Acts as ambassador for the company and contributes to making the sponsor the preferred partner. Performing on-site monitoring visits according to plan, document actions and follow up on action plansSite feasibility visits incl.

analysis of site logistics, site personnel performance/quality indicators and accountability for patient recruitment strategiesTrain and guide site staff in the protocol and trial procedures to minimise protocol deviations (PDs)Train site staff in safety information handling and systemsIdentify potential risks and proactively take action to prevent or mitigateCollaborate with Data Management/logistics in resolving queriesCollection and management of essential documentsSupport the site in filing and archiving trial documentation in the Investigator Trial Master File (ITMF)Participation in Investigators Meetings to ensure relations with sites as well as active presentation as applicableRequirementsBachelor or master degree in Life Sciences or equivalentMinimum of 6 months' previous experience as a CRA in independent on-site monitoring of clinical trialsAbility to work occasionally from the sponsor's officeAbility to build and maintain relationships with sitesHigh focus on delivery and qualityExcellent communication and negotiation skillsEnglish verbal and writing skills, e.

g. enabling understanding of the protocol and study documents as well as writing monitoring reportsWhat ICON Can Offer YouOur success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples IncludeVarious annual leave entitlementsA range of health insurance offerings to suit you and your family’s needsCompetitive retirement planning offerings to maximise savings and plan with confidence for the years aheadGlobal 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-beingLife assuranceFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among othersVisit our careers website to read more about the benefits of working at ICON: https: //careers. iconplc.

com/benefitsAt ICON, 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, colour, 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 through the form below. https: //careers. iconplc. com/reasonable-accommodationsInterested 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 here at ICON whether it is for this or other roles.