Job Title: Associate – Regulatory Affairs
Employment Type: Full Time (Permanent)
Location: Bengaluru, India
Experience: 0 to 1 Years
About ClinChoice
ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology to help our partners advance healthcare by accelerating clinical trials with data-driven insights, delivering the best strategies for product registration, and enhancing patient safety through real-world and clinical analysis. Our global delivery network has expanded to centers and satellite offices in the United States, Mexico, the United Kingdom, Armenia, China, Japan, India, and the Philippines, helping our customers maintain regulatory compliance locally and globally. We have forged future-defining partnerships with industry bodies and technology companies to develop cutting-edge solutions that deliver our expertise with quality and precision.
Key Responsibilities
• Collate data from primary/secondary data sources or stakeholders and maintain databases and data systems
• Interpret data, analyze results using statistical techniques, and provide summary reports
• Develop and implement databases, data collection systems, data analytics, and other strategies that optimize operational efficiency and quality
• Work closely with cross-functional teams to collate data requirements for analysis projects aligned with business processes
• Identify, analyze, and interpret trends or patterns in complex data sets
• Work closely with management to prioritize business and information needs
• Prepare dashboards for management meetings
• Identify opportunities for process improvement
Skills and Qualifications
• Bachelor’s/Master’s degree in Pharmacy/Life Sciences
• Experience with RIMS platforms and regulatory data management is desirable
• Experience with data visualization tools (Tableau, Power BI)
• Proven working experience of 0–1 years in data analysis, data cleaning, and validation, preferably in the pharma/life sciences industry
• Technical expertise in data models, database design and development, data mining, and segmentation techniques
• Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy
• Ability to work independently and collaboratively in a fast-paced environment
• Excellent communication skills
ClinChoice Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ClinChoice and has not been reviewed or approved by ClinChoice.
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Flexible Benefits — Flexible arrangements, including telecommuting and flextime with no core hours in some regions, are highlighted for many roles. Feedback suggests flexibility is commonly available but depends on role and location.
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Leave & Time Off Breadth — Vacation, personal, and sick days are part of the core package, with some markets granting paid leave from the date of hire. Feedback suggests time off is standard-to-decent across locations, though specifics vary.
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Healthcare Strength — Health coverage is positioned as a core benefit, with some accounts describing overall benefits as full or good. In the U.S., healthcare sits within a conventional CRO package alongside medical, dental, and vision.
ClinChoice Insights
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What We Do
ClinChoice is a global full-service Contract Research Organization (CRO) specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies, aiming to accelerate the development and commercialization of innovative drugs and devices.
