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Information & Communication Technology 🏢 Full Time ⭐️ Terverifikasi

Programmer Analyst - Clinical Research & SAS

Thermo Fisher Scientific
Manila City, Metro Manila
Estimasi Gaji
PHP 65.000 – PHP 120.000
Live Update
28 Mei 2026
Batas Akhir
28 Mei 2027

Deskripsi Pekerjaan

Are you a detail-oriented programmer passionate about life sciences? Thermo Fisher Scientific is seeking a skilled Programmer Analyst to join our Clinical Research team in Manila. In this role, you will play a pivotal part in the drug development lifecycle, leveraging your expertise in SAS programming and data analysis to drive bioinformatics innovation and ensure high-quality clinical trial outcomes.

You will work in a high-impact environment, collaborating with global teams to develop clinical datasets, reports, and visualizations that support vital regulatory submissions. If you thrive on solving complex technical challenges and want to make a tangible difference in global healthcare, we invite you to advance your career with a world leader in serving science.

Tanggung Jawab

  • Develop, test, and maintain high-quality SAS programs for clinical data reporting and analysis.
  • Transform complex raw clinical trial data into CDISC-compliant datasets (SDTM/ADaM).
  • Generate tables, listings, and figures (TLFs) in accordance with clinical study protocols.
  • Validate clinical database exports and perform data cleaning activities to ensure integrity.
  • Collaborate with biostatisticians and clinical data managers to meet project timelines and regulatory requirements.
  • Troubleshoot and resolve technical issues within the programming environment.
  • Maintain documentation for all programming activities, ensuring compliance with SOPs and industry regulations.

Kualifikasi

  • Bachelor’s degree in Computer Science, Statistics, Mathematics, Bioinformatics, or a related field.
  • Minimum of 2-4 years of professional experience in SAS programming, preferably within the CRO or Pharmaceutical industry.
  • Strong technical proficiency in SAS/BASE, SAS/STAT, and SAS/GRAPH.
  • Solid understanding of clinical trial design and regulatory reporting (CDISC standards, FDA/EMA guidelines).
  • Exceptional analytical and problem-solving skills with high attention to data accuracy.
  • Effective communication skills with the ability to work in a cross-functional, global team environment.
  • Proficiency in SQL or additional programming languages (R or Python) is a significant advantage.

Keahlian yang Dibutuhkan

SAS Clinical Research CDISC SDTM ADaM Clinical Data Management Statistical Programming Bioinformatics Data Analysis SQL

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