Programming Manager

Work as a Programming Manager across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines, producing, reviewing and updating complex dataset specifications (including efficacy); creating and debugging complex macros; reviewing Statistical Analysis Plans (SAPs), including study specific ISS/ISE and DSMB SAPs and output shells with a view to commenting from a programming perspective. Excellent team work ethos, proactive at managing workload, willingness to help others and learn new skills from working in a team environment. Line managing members of staff, contributing to management meetings. The role will be full-time and fully remote, the successful candidate will be based in India. 

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

Essential:

• Strong SAS programming expertise, including SAS/BASE, SAS/STAT, SAS/GRAPH and ODS. Experience with additional SAS modules, automation tools or other programming languages would be advantageous.
• Educated to BSc or above within Computer Science, Mathematics or a Science related discipline
• Strong knowledge of CDISC standards, particularly SDTM and ADaM, including dataset specifications, implementation, validation and regulatory submission requirements.
• Experience leading statistical programming activities, including study planning, resource allocation, timeline management, quality oversight and technical review.
• Ability to provide technical guidance and mentoring to programmers while working effectively with statisticians, data managers and cross-functional study teams.

Preferred:

• Experience supporting complex efficacy analyses, including advanced statistical outputs, derived endpoints, sensitivity analyses and exploratory or post-hoc analyses.
• Experience leading programming activities for complex clinical studies, integrated analyses or regulatory submissions.
• Ability to work with overlap with US morning hours

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.

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