ClinChoice
pharmaceutical, medical device, and consumer care
Associate-RegulatoryAffairs
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“Associate - Regulatory Affairs at ClinChoice. Skills: data analysis, data cleaning, validation, regulatory data management. 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”
What You'll Achieve.
optimize operational efficiency and quality; accelerating clinical trials with data-driven insights; delivering the best strategies for product registration; enhancing patient safety through real-world and clinical analysis; maintain regulatory compliance locally and globally
Industry & Context.
analytical skills; attention to detail and accuracy
What They're Looking For.
Must Have
Bachelor’s/Master’s degree in Pharmacy/Life Sciences, 0–1 years in data analysis, data cleaning, and validation, analytical skills, Ability to work independently and collaboratively, Excellent communication skills
Nice to Have
Experience with RIMS platforms and regulatory data management, experience in the pharma/life sciences industry
What You'll Do.
Collate data from primary/secondary data sources or stakeholders and maintain databases and data systems
analyze results using statistical techniques
and provide summary reports
Develop and implement databases
data collection systems
and other strategies that optimize operational efficiency and quality
and interpret trends or patterns in complex data sets
Prepare dashboards for management meetings
Identify opportunities for process improvement
How You'll Work.
Team & Collaboration
Work closely with cross-functional teams to collate data requirements for analysis projects aligned with business processes; Work closely with management to prioritize business and information needs; Ability to work collaboratively in a fast-paced environment
Communication Scope
Excellent communication skills
Full Job Description
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
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