Senior Sas Programmer

THE ROLE

Demand for our Functional Service Provision is growing we are therefore looking for a driven and passionate Statistical Programmer to join our reputable FSP team to support one of our fantastic US based pharmaceutical clients. We are looking for an experienced Programmer with ISS / ISE and submission experience, who is versatile and flexible to work on various therapeutic areas. The successful individual must be able to program / QC ISS and ISE datasets, as well as TLFs – and will have experience with building macros and standards.

This is a fantastic opportunity to work for a growing CRO that is recognized for its continuous learning and development opportunities, whilst also gaining direct experience of working within a pharmaceutical environment.

This position is remote, and the successful candidate can be located anywhere in India.

Responsibilities:

Employees may be required to perform some or all of the following...

Program and validate SDTMs and ADaMs, including complex efficacy, labs, etc.

Program complex non efficacy outputs/figures

Develop and debug complex macros

Create, QC and update complex dataset specifications (including efficacy) for single/ multiple studies

Review simple study design SAP without supervision

Review all shells without supervision and provide feedback

Knowledge, interpretation and implementation of current SDTM, ADaM standards

Knowledge of FDA CRT requirements including define.xml and define.pdf

Become familiar with and follow study documentation

Ensure the principles in the Phastar checklist are followed rigorously

Archive study documentation following instructions in supplied SOPs

Act as a Lead Programmer, ensuring quality and timely delivery

Liaise with the Study Statistician and Project Manager regarding resourcing and deliverables

Assess and monitor study level resources

Point of contact for programming issues for the team, proactively ensuring everything is working cohesively

Persuade stakeholders to follow best practice within a trial

Assist in development of internal training courses

Qualifications:

Educated to BSc or above within Computer Science, Mathematics or a Science related discipline

5+ years of CDISC standards experience (i.e. programming SDTMs and ADaMs)

5+ years of SAS programming experience within the pharmaceutical/CRO industry (essential)

ISS/ISE experience (essential)

Excellent communication skills

Good awareness of clinical trial issues, design, and implementation

Familiarity with GCP and regulatory requirements

Oncology experience is strongly preferred. Candidates without oncology experience must have prior experience working on complex efficacy studies.

APPLY NOW

With the world’s eyes focused on clinical trial data, this is a fantastic time to join an award-winning specialized biometric CRO that is renowned for its technical expertise, outstanding quality and cutting-edge data science techniques. We offer flexible working, part-time hours, structured training and development plans, continuous learning opportunities, and a competitive salary and benefits package. We’re committed to ensuring our employees achieve a healthy work-life balance, within a supportive, fun and friendly working environment.

Should you feel that you have the right skill set and motivations for this position, please apply! Please note that we are considering candidates located anywhere in India as this role can be carried out remotely.

Phastar is committed to the principles and practices of equal opportunities and to encouraging 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, colour, 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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