Medical writing and clinical services for pharma drug development and safety
SIRO operates two integrated business units serving pharmaceutical companies: medical writing (protocols, regulatory documents, clinical trial transparency, scientific publications) and clinical services (staffing, data management, pharmacovigilance). The tech stack reveals active modernization — Oracle + SAP for core systems, Databricks + PySpark for data pipelines, and emerging adoption of OpenText — alongside heavy engagement with SDTM/ADAM dataset specifications and data warehouse initiatives. The hiring mix (senior data and engineering roles concentrated in India) suggests internal platform investment to automate document workflows and scale data operations for a growing client base.
SIRO is a privately held pharmaceutical services firm founded in 1996, headquartered in Mumbai with 201–500 employees. The company serves global pharma and IT firms across clinical development, drug safety, and regulatory functions. SIRO Medical Writing handles regulatory documentation (protocols, clinical study reports, eCTD modules), clinical trial transparency services (protocol registries, document redaction, lay summaries), scientific publications, real-world evidence analysis, and post-market safety surveillance. SIRO Clinpharm provides staffing and flexible workforce solutions for clinical operations, data management, biostatistics, and pharmacovigilance. Active projects span research information management, HR document automation, data ingestion pipelines, and SDTM/ADAM dataset development for clinical trials.
Oracle, SAP Master Data Governance, Databricks, AWS, Java, Python, SAS, SQL, Shiny, React, Angular, and ServiceNow for HR and operations. Recently adopting OpenText for document management.
Mumbai, Maharashtra, India. The company was founded in 1996 and is privately held with 201–500 employees.
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