Clinical trial coordinator

## Clinical Trial Coordinator Applyremote type: Hybridlocations: Verona: Verona-Remotetime type: Full timeposted on: Posted Todayjob requisition id: JR000583**Are you being referred to one of our roles by a connection in Alira Health?** If so, please apply using the referral link emailed to you. Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.**Job Description Summary****Job Description**## ROLEThe Clinical Trial Coordinator assists the clinical research team ensuring to conduct study in accordance to GCP, SOP, protocol, and in respect of budget and timelines. The Clinical Trial Coordinator is responsible of start up activities and documents management. ## KEY RESPONSABILITIES* Responsible (under PM oversight) of start up activities, including Ethic and Regulatory submission (at national and international level) and sites contracts’ negotiation.* Responsible for ISF preparation and TMF set up and maintenance (under PM oversight).* Maintains relationship with ECs and CA.* Supports in sites/vendors invoicing management and responsible to maintain an appropriate tracking if required.* Collaborates with the preparation of weekly/monthly and ad hoc project reports, also updating CTMS and maintaining study-specific trackers as needed.* Supports with CRAs activities follow-up.* Supports with document translation, if required.* Participates in internal, client/sponsor, scientific, and other meetings as required; participates to audit.* Performs additional duties as assigned## DESIRED QUALIFICATION & EXPERIENCE* Graduation in scientific/health field* Previous experience in clinical research (in CROs, Pharma or academy/hospital experience)* Good knowledge of ICH GCP and appropriate regulations* Good knowledge of Clinical Research and Regulatory/Ethical requirements## TECHNICAL COMPETENCES & SOFT SKILLS* English, good* MS Office Suite, Good* Professional* Trustworthy* Quality focused; ability to be careful, thorough, and detail-oriented* Strong organizational skills and the ability to multi-task and work effectively in a fast-paced environment; able to manage priorities and organize time* Strong analytical skills* Strong communication and interpersonal skills with customer service orientation**Languages**English**Education**Bachelor of Science (BS): Life Sciences, Bachelor of Science (BS): Pharmacy **Contract Type**Regular **Salary Range** The final offer will be determined within the applicable location-specific range and will depend on the candidate’s confirmed work location, relevant experience, skills, qualifications, internal equity, and role scope.€ 30,000 - € 35,000### About Us Alira Health is a global advisory firm providing consulting and research and clinical development services whose mission is to humanize healthcare and life sciences, in partnership with patients, through innovative technologies and expert guidance. From development to medical care, we complement the expertise of our Pharma, Biotech, and Med Tech clients with a full spectrum of services across their entire solutions lifecycle.### Why Work at Alira Health?With offices around the world, Alira Health provides a vibrant and creative environment with benefits that include professional development, global travel, flexible work programs and more. We welcome your passion and drive, talent and entrepreneurial spirit, sense of service and teamwork.### Join Our Team We are an integrated team of over 800 scientists, strategists, economists, clinicians, and biostatisticians representing over 30 nationalities. This broad global perspective and cultural richness has a direct impact on providing innovative solutions for our clients that lead to higher standards of care and an improved patient experience. #J-18808-Ljbffr