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Veramed

Principal SAS Programmer - Bangalore/Hyderabad/Rest of India (Remote)

Early Applicant
  • 4 months ago
  • Be among the first 50 applicants

Job Description

We believe in hiring not only the best quality candidate but also the best fit for our culture and vision for the future. Our retention rate and employee satisfaction are high for a reason: we develop our staff and give them a work-life balance that not only improves their happiness but also their productivity and quality of work. Being a new CRO in the Indian market, it is an exciting time to consider roles with us. Are you looking to join a company that truly puts its people first

Company Overview

Veramed is a specialist CRO to the pharmaceutical industry, focused on delivering high quality statistics and programming to the reporting of Phase I-IV clinical trials across a variety of therapeutic areas. We are currently looking for experienced Principal SAS Programmers to join us and take on hands-on programming responsibilities. This is an opportunity to join an FSP-style model with a global best in class organization.

Benefits of the Role

This role offers a competitive salary and annual bonus, health insurance, training and a great working culture. As we are a small company you will have the opportunity to be a key part of our growth and to develop a wide range of skills. Our commitment is to challenge, encourage and support you to help you reach your full potential. We offer flexible working arrangements, which will be discussed in an initial screening call.

Key Responsibilities

The job tasks listed below outline the scope of the position. The application of these tasks may vary, based on current business needs.

Technical:

  • Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs.
  • Author, review and approve study TFL shells and dataset specifications.
  • Author, validate and document SAS programs for datasets, TFLs and macros, applying good programming practice.
  • Identify data issues and outliers.
  • Complete, review and approve CDISC Validation tool reports.
  • Identify data and standards issues and resolve or escalate as appropriate.
  • Awareness of emerging standards and associated impact to ongoing and future planned trials.
  • Maintain proficiency in SAS and awareness of developments.
  • Maintain study master file documents and any other documents that are required to be audit ready.

Qualifications, Skills & Attributes:

  • 7+ years of relevant experience.
  • BSc, MSc or PhD (or equivalent) in Mathematics, Computer Science or other analytical field.
  • Proficient SAS programming skills: good knowledge of SAS/BASE.
  • Knowledge or training in CDISC (SDTM & ADAM).
  • Excellent verbal and written communication skills.
  • Excellent organisational and problem-solving skills.
  • Ability to establish and maintain effective working relationships with co-workers, managers and clients.
  • Self-management skills, with a focus on timely and accurate completion of competing deliverables.
  • Candidates must have the legal authorisation to work in India.

What to expect:

  • A warm, friendly working environment in which to thrive both personally and professionally.
  • A supportive, open-door management policy that will aid in your development and provide you with the tools to take your career to the next level.
  • A truly unique CRO that's doing something different when it comes to managing staff, projects and building relationships in the industry.
  • The ability to own your role and develop your skills and experience.

If this role sounds right for you, please click apply now to submit your application. We'd love to hear from you!

More Info

Industry:Other

Function:Pharmaceutical

Job Type:Permanent Job

Skills Required

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Date Posted: 11/07/2024

Job ID: 84135729

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