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Hiring SAS Programmers in Pharma – Bioclinica Careers – Remote Opportunity

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Bioclinica

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Computer Science or related field.

Remote (India)

1 - 3 Years

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Bioclinica is a leading clinical research and technology-driven solutions provider specializing in medical imaging, eClinical technologies, and drug development services. Committed to innovation and quality, Bioclinica supports pharmaceutical and biotech companies in bringing new therapies to market efficiently.

As an equal opportunity employer, Bioclinica fosters a diverse and inclusive work environment, encouraging professional growth and collaboration.


Detailed Job Description

Job Title: Clinical Data Programmer

Location: Remote (India)
Job Type: Full-time
Requisition ID: R16197

Primary Responsibilities:

  • Develop and execute SAS edit check programs for clinical data validation.
  • Create and validate SAS programs, macros, and ad-hoc reports for internal/external use.
  • Ensure data accuracy and integrity by reviewing data export specifications.
  • Apply CDISC SDTM guidelines for clinical data transfers.
  • Collaborate with Clinical Data Managers (CDMs) and project teams to meet reporting needs.
  • Maintain programming documentation in compliance with Good Clinical Practices (GCP).
  • Contribute to SOP development and process improvements.

Secondary Responsibilities:

  • Assist in resolving technical issues related to clinical data.
  • Participate in training and knowledge-sharing initiatives.
  • Support team members in achieving project goals.

Eligibility & Qualifications

Education:

  • Bachelor’s or Master’s degree in Computer Science, Life Sciences, or related field.
  • SAS Certified Professional (preferred but not mandatory).

Experience:

  • 3+ years of SAS programming in the pharmaceutical/clinical research industry (1 year for Master’s degree holders).
  • Familiarity with CDISC, SQL, and relational databases.
  • Strong data analysis and problem-solving skills.
  • Knowledge of medical/clinical trial terminology (advantageous).

Key Skills:

✔ Advanced SAS programming
✔ Clinical data management (CDM)
✔ CDISC SDTM compliance
✔ Data validation & reporting
✔ Strong analytical abilities
✔ Excellent communication & teamwork


Benefits & Work Environment

✅ Remote work opportunity (India-based)
✅ Competitive salary & growth prospects
✅ Inclusive & supportive workplace culture
✅ Professional development & training
✅ Flexible & collaborative team environment

Working Conditions:

  • Travel: Minimal (0-5%)
  • Physical Requirements: Light (0-10 lbs lifting, prolonged computer work)

How to Apply

Application Link