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Principal Programmer Analyst (Pharmacovigilance)

0-2 years
Not Disclosed
10 March 24, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Principal Programmer Analyst (Pharmacovigilance) - Remote, India
 

Overview:
Thermo Fisher Scientific Inc. is seeking a Principal Programmer Analyst (Pharmacovigilance) to lead programming strategies for clinical trials, ensuring data integrity, accuracy, and compliance with industry standards.

Key Responsibilities:

  • Develop and execute programming strategies for clinical trials.

  • Collaborate with cross-functional teams to determine effective programming solutions.

  • Ensure integrity and accuracy of trial data through rigorous validation processes.

  • Implement innovative programming techniques to streamline trial processes.

  • Provide mentorship to junior programmers, fostering continuous improvement.

  • Stay updated with industry trends and technological advancements.

Requirements:

  • Proven experience as a trial programmer in the information technology sector.

  • Strong attention to detail and commitment to delivering high-quality results.

  • Ability to adhere to regulatory guidelines and industry standards.

  • Strong problem-solving skills and adaptability to evolving project requirements.

  • Bachelor's degree in Computer Science, Information Technology, or related field preferred.

Work Schedule: Standard (Mon-Fri)
Location: Fully Remote, India