- Location
- , CN
- Department
- Management
- Seniority
- Senior
- Closing date
- Today
- Source
- iCIMS
Description
Overview
Work as a senior data coordinator on clinical and non-clinical trials; producing and validating eCRFs and databases to excellent quality whilst adhering to deliverable timelines. Producing, reviewing and updating eCRF specifications and sections of the Data Handling Manual. Leading clinical coding activities and management of third party data and eCRFs in order to produce a clean database. Acting as lead Data Manager on assigned studies. Working closely with the Sponsor's study team and third party suppliers to meet project deliverables and timelines. Excellent team work ethos, able to manage workload of others, willingness to help others, share skills in a team environment and contribute to process improvement and company profile.
Responsibilities
Employees may be required to perform some or all of the following:· Taking responsibility for data management study deliverables within reporting teams for complex studies. Preparing content of slides for Kick off Meetings · Acting as the Lead DM ensuring quality and timely delivery of DM aspects of study. Liaising with Lead Programmer, Lead Statistician and Study Project Lead regarding resourcing and deliverables · Leading DM teams to ensure quality and timely delivery of more complex deliveries on Phastar projects or client studies. Liaise with stakeholders to ensure successful project delivery · Being point of contact for DM issues for the team. Managing own day-to-day workload to ensure all project goals are met and taking responsibility for study level · Mentoring less experiences team members. Helping others as and when required, proactively assisting less experienced team members on an ad-hoc basis · Ensuring clients (internal and external) remain engaged and well informed. Maintaining a positive client relationship
Qualifications
· Life Science degree, nursing qualification or equivalent experience· Good awareness of clinical trial issues, design, and implementation.· Familiarity with GCP and regulatory requirements· Experience of data management software systems and some experience of leading data processing activities within a regulated environment
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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