Work as a senior data operations programmer on clinical and non-clinical trials; develop and maintain trial specific databases, including eCRF’s, edit Checks and Custom Functions using relevant programming languages of various levels of complexity to excellent quality whilst adhering to deliverable timelines. Creation of advanced custom programs as per Data Review Convention specifications as required. Program reports and listings which contribute to the standardization of process and reports used for data review and analysis for external partners/vendors. Develop and maintain CDASH compliant therapeutic area and global eCRF libraries ensuring efficient mapping to current SDTM standards. Good knowledge of CDISC CDASH and SDTM implementation guidelines. Excellent teamwork ethos, willingness to help others and learn new skills from working in a team environment.
Responsibilities
Employees may be required to perform some or all of the following:
- Participate in study specific eCRF programming strategy meeting at study set up.
- Perform senior review of database specification documents created by study teams, such as eCRF specifications and Data Review Convention specifications.
- Build clinical study database CRF database screens per CRF/database specifications provided by the study team.
- Create/Program edit checks, special action and derivations as per the Data Review Convention specifications.
- Ensure non -eCRF technologies for data capture (e.g., ePRO, coding, IWRS/RTSM) are deployed as per requirements, including integrations with other systems, platforms or reporting environments with timelines for consumable data outlined.
Qualifications
- University or college degree in Life Sciences, Mathematics, Computer Science or equivalent degree
- At least 5 years’ experience in clinical database programming, setup of clinical databases and eCRF design, edit checks, Custom Function and Migration, gained in the pharmaceutical industry, CRO or Life science related industry
- Certification in Medidata Rave EDC
Why Join Us
- Remote working and flexible working hours
Career development, mentorship, and continuous learning
Supportive, friendly, and collaborative culture
Making a Positive Impact: we are committed to sustainability, solid responsibility and strong ethical governance through our ESG initiatives
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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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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