In House CRAICONs Clinical Operations team is actively looking to hire a significant number of In-house CRAs. You will be part of our world class development program which fast tracks your growth into a traveling CRA within 4-6 months. If you enjoy travel, are ready for your next step in your clinical research career, and are passionate about ICONs mission to bring life-saving therapies to market, this is your chance to join the team ICON’s award-winning study execution capabilities have led to the approval of 18 of the world’s top 20 best-selling drugs.
As a global provider of drug development solutions, our work is serious business. But that doesn’t mean you can’t have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry.
Are you one of them? Apply Now.The RoleBecome familiar with ICON’s SOPs/WPs, ICH GCP guidelines, appropriate regulations, ICON systems and the principles of and assist with investigator recruitmentMaintain timelines and ensure accuracy and completeness of data entered into ICON systemsServe as the primary in-house contact for sites and investigators participating in studiesConduct and completes remote site management activities, with support as needed, according to applicable SOPS and the Study Monitoring Plan.
To contact Clinical sites for specific requests (e.g. enrolment updates, missing documentation, data entry timeliness, data query follow-up, CDA finding follow-up, and action Item resolution or other sponsor specific CRA tasks.
Take responsibility for project tasks and sees these tasks through to successful completion, with support.Maintain a professional interpersonal relationship with study team, sites, and SponsorsParticipate in QA Audits as needed.Regularly attend and gives to project specific and departmental meetingsAbility and willingness to travel as needed (drive and fly)Maintain Sponsor and patient confidentialityOther duties as assignedWhat you needMinimum Bachelor’s degree in a life scienceAt least 12 months of a CTA/Clinical Trial Assistant or similar role experience within the clinical/pharmaceutical industryUnderstanding of ICH GCP ComplianceExcellent communication and organizational skillsA phenomenal teammateBenefits of Working at ICONOther than working with an outstanding team of ambitious people, we also offer a very competitive compensation package.
We provide a range of health-related benefits to employees and their families and offer competitive retirement plans-But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.We care about our employees as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
ICON is an equal opportunity employer and committed to providing a workplace free of any discrimination or harassment.EOE race/color/religion/sex/sexual orientation/gender identity/disability/vet/national originFull time
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