Principal Programmer Analyst (Pharmacovigilance) – Fully Remote
📍 Location: Remote, India
📌 Job ID: R-01288376
💼 Job Type: Full-time
🔬 Category: Clinical Research
About Us
Join Thermo Fisher Scientific Inc. and contribute to cutting-edge clinical research that drives pharmacovigilance and drug safety advancements. As part of our PPD® clinical research portfolio, we are a leading global contract research organization (CRO) dedicated to bringing innovative therapeutics to market.
Work Schedule
🕘 Monday – Friday (Standard Office Hours)
🏢 Fully Remote Work Opportunity
About the Role
As a Principal Programmer Analyst (Pharmacovigilance), you will lead the design, development, and execution of programming solutions for clinical trials, ensuring the accuracy, integrity, and compliance of trial data. This role requires expertise in data programming, validation processes, and clinical trial workflows, along with a strong ability to mentor junior team members.
Key Responsibilities
✅ Lead Programming Strategies: Develop and implement high-quality programming solutions for clinical trials, ensuring compliance with regulatory standards.
✅ Cross-Functional Collaboration: Work closely with clinical teams, data management, and statisticians to deliver optimized programming solutions.
✅ Data Validation & Integrity: Maintain data accuracy and reliability through rigorous quality control and validation processes.
✅ Innovation & Optimization: Introduce cutting-edge programming techniques to enhance trial efficiency and streamline processes.
✅ Mentorship & Leadership: Guide and mentor junior programmers, fostering a culture of excellence and continuous learning.
✅ Stay Ahead of Industry Trends: Keep up with technological advancements and evolving industry standards to maintain a competitive edge.
Who You Are
Education & Experience:
✔ Bachelor’s or Master’s degree in Computer Science, Information Technology, Life Sciences, or a related field.
✔ Extensive experience (typically 6+ years) in clinical trial programming within a pharmaceutical, biotechnology, or CRO environment.
Key Skills & Competencies:
✅ Proven experience in clinical trial programming and pharmacovigilance data analysis (6+ years required).
✅ Expertise in SAS programming, SQL, or R for clinical data analysis.
✅ Strong problem-solving skills with the ability to adapt to evolving project requirements.
✅ Thorough understanding of regulatory requirements (e.g., FDA, EMA, ICH-GCP).
✅ Ability to collaborate effectively with cross-functional teams and drive projects to completion.
✅ Excellent attention to detail with a commitment to delivering high-quality results.
Why Join Us?
🌍 Global Impact: Work on high-impact clinical research projects that bring life-changing therapies to market.
📈 Career Growth: Join a leading CRO with endless opportunities for professional development.
💡 Innovation-Driven Environment: Be part of a team that embraces new technologies and innovative programming approaches.
🤝 Collaborative Culture: Work alongside industry experts in a diverse and inclusive workplace.
💼 Join Thermo Fisher Scientific Inc. and shape the future of clinical research with us! 🚀
📩 Apply Now and Make an Impact!
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