Senior Statistical Programmer
Role Overview
Work as a senior programmer on clinical and non-clinical trials; producing complex datasets and outputs to excellent quality whilst adhering to deliverable timelines.
Good knowledge of CDISC SDTM and ADaM implementation guidelines; producing, reviewing and updating complex data specifications; creating and debugging complex macros; understanding Statistical Analysis Plans (SAPs) and output shells for day to day programming activities.
Excellent team work ethos, willingness to help others and learn new skills from working in a team environment.
This role is full-time and fully-remote .
The successful candidate may be based in India .
Key Skills for This Role
Full Job Posting
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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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.
Important notice to Employment businesses/Agencies
Phastar does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Phastar's Head of Talent Acquisition to obtain prior written authorization before referring any candidates to Phastar. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and Phastar. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of Phastar. Phastar shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site .
Requirements
- BSc in Computer Science, Mathematics or a related discipline.
- Strong experience in clinical trial statistics and SAS programming, supporting Phase II/III studies across analysis, reporting, and regulatory submission activities.
- Hands-on expertise in SDTM, ADaM, TLF development and validation, with strong knowledge of CDISC standards and submission-ready deliverables.
- Experience supporting regulatory submissions, including NDA/BLA, MAA, ISS/ISE, eCTD packages, define.xml, reviewers’ guides, and responding to regulatory authority queries.
- Ability to interpret protocols, SAPs, shells, and statistical specifications, translate requirements into high-quality analysis outputs, and identify issues proactively.
- Strong understanding of submission QC, traceability, data integrity, and programming best practices, including independent validation, macro usage, documentation, and adherence to SOPs.
- Proven ability to work independently with statisticians, programmers, data management, medical writing, and sponsor teams, manage timelines, communicate risks early, and deliver high-quality outputs under tight submission deadlines.
- MSc in Mathematics, Computer Science or a related discipline is advantageous.
About Phastar
Specialist biometrics and data science CRO providing clinical-trial data services to pharmaceutical, biotech, and medical-device companies.
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