Xogene is hiring for the position of CTT Specialist – I at its Pune, Maharashtra office. This is a full-time, on-site opportunity designed for Master’s students in Pharmacy or Life Sciences who are expected to graduate in 2026, with onboarding planned for July 2026.
Xogene is a fast-growing global company transforming clinical trial transparency through AI-powered regulatory solutions. This role offers early-career professionals hands-on exposure to clinical trial disclosure, regulatory compliance, plain language summaries, and AI-enabled clinical systems, making it an excellent entry point into clinical research, regulatory affairs, and medical writing careers.
About Xogene
Xogene combines deep regulatory expertise with advanced AI technologies to automate and optimize clinical trial disclosure and transparency workflows. The organization supports global pharmaceutical and life sciences companies by ensuring compliance with US and international clinical trial registries while advancing transparency through innovation.
Job Details at a Glance
- Job Title: CTT Specialist – I
- Company: Xogene
- Location: Pune, Maharashtra
- Employment Type: Full-time, On-site
- Eligible Batch: 2026 pass-outs
- Joining Timeline: July 2026
- Industry: Clinical Research, Regulatory Affairs, Clinical Trial Transparency
Key Responsibilities
As a CTT Specialist – I, you will support Xogene’s Clinical Trial Transparency (CTT) team by:
- Performing data entry and quality review for assigned clinical studies
- Entering and maintaining data in global clinical trial registry systems
- Supporting clinical trial document redaction and anonymization
- Authoring Plain Language Summaries (PLS)
- Reviewing clinical and non-clinical documents for accuracy and compliance
- Tracking project status and coordinating with client-side Disclosure Coordinators
- Researching and applying global clinical trial transparency regulations
- Supporting AI and technology development as a subject matter expert
- Managing timelines and flagging delivery risks proactively
- Assisting with US and international registry postings
- Contributing to process improvement initiatives
Eligibility & Qualifications
To be eligible for this role, candidates must have:
- Master’s degree (M.Pharm / Life Sciences) – graduating in 2026
- Strong interest in life sciences, clinical research, or regulatory affairs
- Excellent organizational and time-management skills
- High attention to detail and quality mindset
- Proficiency in Microsoft Excel, Word, and PowerPoint
- Strong written and verbal communication skills
- Ability to work in global, cross-cultural teams
- Foundational knowledge of drug development or clinical science
- Bachelor’s degree or 2 years of equivalent experience (preferred)
Why Join Xogene?
Xogene offers a high-impact, learning-driven environment with:
- Structured mentorship from industry experts
- Clear career progression in clinical trial transparency
- Exposure to AI, LLMs, and conversational regulatory systems
- Competitive compensation with comprehensive benefits
- A results-oriented, innovation-focused work culture
Estimated Salary (India)
- ₹4.5 – ₹5.5 LPA (Indicative, based on entry-level clinical research roles in Pune)
How to Apply
