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Phastar

Bringing data to life

Senior Data Manager

ManagerManagerOtherRemoteLeadTeam 201-500Since 2007H1B SponsorCompany SiteLinkedIn

Location

United Kingdom

Posted

17 days ago

Salary

0

Seniority

Lead

No structured requirement data.

Job Description

Senior Data Manager

Phastar

Role Description As a Senior Data Manager specializing in clinical trials across multiple sponsors and therapeutic areas, you will lead the study, providing expert data management guidance to the project team and providing study oversight, acting as the primary source of data management expertise and supporting the team in achieving study objectives and ensuring data integrity throughout all phases of the trial. - Data management lead for studies; providing guidance for other data managers on the team, coordinating data processing activities, ensuring clinical databases are correct, delivered on time and budget, and are of excellent quality. - Implement CDASH standards, produce and review CRF specifications following the CDASH implementation guide. - Work in a team for furthering data capture systems development. - Attend project teleconferences and ensure assigned actions are completed within the required timeframe. - Actively participate (including presentations) at project Kick Off meetings and Clinical Trial Team meetings for the assigned trials, ensuring appropriate level of support and communication provided. - Liaise with Study Statistician and Study Project Manager regarding resourcing, timelines, and deliverables. - Be point of contact for data management issues for the team across multiple studies. - Provide support for Data Safety Monitoring Board and all other vendors, including training of Investigators, site staff, and the client’s internal teams. - Work in a cross-functional team environment in experience-appropriate studies; identifying issues, giving solutions, and advising on cross-functional issues throughout study conduct. - Ensure effective communication between functional teams and with the client, providing a high level of client satisfaction through successful execution of projects. Qualifications - Experience working within a clinical trials environment (CRO, pharma or academia). - Previous experience in Medidata Rave. - Experience in CDISC. Benefits - Remote working and flexible working hours. - Career development, mentorship, and continuous learning. - Supportive, friendly, and collaborative culture. - Making a Positive Impact: As a B-Corp™ organization, we are committed to sustainability, solid responsibility and strong ethical governance through our ESG initiatives.

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