Clinical Data Coordinator II

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.

About the Role

Work as a Data Coordinator II/III on clinical and non-clinical trials; working as part of the study team, taking part in specifying, programming and User Acceptance Testing of eCRFs and edit checks; producing and reviewing sections of the Data Handling Manual. Performing clinical coding activities and management of third-party data, reviewing data listings and eCRFs and actioning queries in order to produce a clean database. Taking responsibility for all DM deliverables and where assigned act as the Lead Data Manager for non-complex studies. Excellent teamwork ethos, proactive at managing workload, willingness to help others and share skills in a team environment and contribute to process improvement and company profile. This role is full-time and fully-remote. The successful candidate may be based in China.

Responsibilities

• Statistical expertise and scientific leadership
• Leadership and people development
• Compliance, quality and governance
• Communication and influence

Qualifications

• The ability to review data using SAS listings & Excel, including SAE reconciliations and coded data listings
• Database testing experience within Medidata Rave, reviewing edit check outputs and actioning as appropriate
• Familiarity with the reviewing of draft documents for third party data, updating documents and reviewing reconciliation outputs
• The ability to produce status reports
• Experience working within a clinical trials environment (CRO, pharma or academia)
• Experience and familiarity with CDISC standards
• Experience with Medrio, Viedoc or CrsCube is advantageous

Why Join Us

• Remote working and flexible working hours
• Career development, mentorship, and continuous learning
• Supportive, friendly, and collaborative culture