Senior Clinical Research Associate Contractor

Allucen is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them. Allucent is a non-laboratory environment.

We are currently recruiting for an Italian-speaking Senior Clinical Research Associate (sCRA) to join our team in Italy. The Senior Clinical Research Associate (sCRA) coordinates and performs site management and monitoring activities within the Site Management department of Allucent’s Clinical Trial Operations. The SCRA monitors site performance and provides mentoring to CRA trainees/CRA I-II study team members. The SCRA acts as the main line of communication between the participating sites and the Lead CRA/PM

Location: Italy

Therapeutic area: Oncology

Responsibilities:

• Perform initiation visits to train and instruct site staff on the study specific requirements
• Assist in site activation
• Perform Monitoring visits to:
• Verify that source data and study database are accurate, complete and maintained properly
• Verify subject eligibility
• Verify protocol compliance, including safety reporting and drug handling
• Verify all study files are maintained and up to date
• Support site staff in preparation for study specific site audits and inspections
• Perform Close-out visits
• Perform Pre-study visits, if delegated by SSU
• Perform centralized and risk based monitoring activities
• Act as the main line of communication between the study PM/LCRA and the site staff
• Maintain study related trackers
• Prepare site visit reports
• Liaise with site staff to achieve patient recruitment targets
• Contribute to the development of study specific documents
• Support the study start-up team in preparation of the submission packages and collection of site documents, if delegated by SSU
• Actively support site management staff learning & development within the company

Requirements

Qualifications:

• Life science, healthcare, medicine and/or related degree
• Minimum 3+ year of CRA experience
• Minimum 3 years of experience in drug development and/or clinical research
• Good knowledge of ICH-GCP, privacy legislation (GDPR and/or HIPPA), regulations (CTR/CTD and/or CFR), and applicable local regulatory requirements
• Good understanding of site management and monitoring
• The ability to perform site visits in an effective way and according to high quality standards

Skills:

• Strong written and verbal communication skills including good command of Italian and English
• Representative, outgoing and client focused
• Ability to work in a fast-paced challenging environment of a growing company
• Administrative excellence with attention to detail and accuracy
• Proficiency with various computer applications such as Word, Excel, and PowerPoint required
• Strong organizational skills

To all recruitment agencies: Allucent does not accept agency resumes. Please do not forward resumes to our careers alias or other Allucent employees. Allucent is not responsible for any fees related to unsolicited resumes.

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