Clinical Data Coordinator II/III

Overview

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

The following areas of expertise will be aligned to the role...

• 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

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

Apply Now

Be part of a team known for technical expertise, quality, and impact. We value Excellence, Collaboration, Integrity, Innovation, and Passion—and we seek team members who embody these qualities. Apply today!

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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