Overview
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.

Responsibilities

• 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

Why Join Us
Remote working and flexible working hours
Career development, mentorship, and continuous learning
Supportive, friendly, and collaborative culture

About Phastar
Phastar is an award-winning biometrics and data science CRO, trusted by pharma, biotech, and medical device companies worldwide. With a global team of data specialists, we bring expertise, precision, and pace to every trial, because behind every data point is a patient waiting for treatment.
We transform complex data into clear, actionable intelligence, helping accelerate drug development, and bring life-changing therapies to patients faster.

Awards & Recognition

• SCRIP – Best Contract Research Organization, Specialist Provider
• Citeline – 2025 Award Winner
• Fierce CRO Awards – Recognized Industry Leader

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Phastar is committed to the principles and practices of equal opportunities and to encourage the establishment of a diverse workforce. It is our policy to employ individuals on the basis of their suitability for the work to be performed and their potential for development, regardless of age, sex, race, color, nationality, ethnic or national origin, disability, marital status, pregnancy or maternity, sexual orientation, gender reassignment, religion, or belief. This includes creating a culture that fully reflects our commitment to equal opportunities for all.

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