CTT Specialist I – Clinical Trials Transparency (Postgraduates – 2026 Passouts)
Location: Gurgaon, Haryana, India (Hybrid)
Employment Type: Full-Time
Function: Clinical Trials Transparency
Industry: Life Sciences | Regulatory Compliance | AI-Enabled Solutions
About Xogene
Xogene is transforming the future of clinical trial transparency through advanced AI-powered regulatory solutions. The company partners with leading pharmaceutical and life sciences organizations to streamline global clinical trial disclosure, ensuring regulatory compliance across multiple jurisdictions. By combining deep regulatory expertise with cutting-edge technology, Xogene delivers efficient, scalable, and future-ready transparency solutions.
Role Overview
Xogene is hiring a CTT Specialist I to join its Clinical Trials Transparency (CTT) team. This entry-level role is specifically designed for postgraduate students graduating in 2026 who are passionate about life sciences, regulatory compliance, and emerging AI technologies. The role offers hands-on exposure to global clinical trial disclosure activities, regulatory intelligence, and AI-enabled process optimization.
Key Responsibilities
Support the CTT team with data entry and documentation activities for assigned clinical studies.
Enter and manage clinical trial data within global and local registry systems in compliance with regulatory requirements.
Perform quality checks and content reviews to ensure accuracy, consistency, and completeness of submitted data.
Support clinical document redaction and anonymization projects to protect confidential and personal information.
Author Plain Language Summaries (PLS) in alignment with regulatory and patient-centric standards.
Track project status and coordinate with client-side Disclosure Coordinators when required.
Develop subject matter expertise in global clinical trial transparency regulations through research and application of regulatory guidance.
Support technology enablement and AI development initiatives by providing regulatory subject matter expertise.
Proactively manage deliverables and escalate timeline risks to project coordinators and management.
Support administrative activities related to US and international clinical trial registry postings and results disclosures.
Contribute to continuous process improvement initiatives and provide constructive feedback to team members.
Required Qualifications & Experience
Education:
Master’s degree students completing post-graduation in 2026 (Life Sciences, Pharmacy, Clinical Research, Biotechnology, or related discipline).
Bachelor’s degree in a relevant field is mandatory.
Experience:
Entry-level role; 0–2 years of relevant academic, internship, or industry experience in life sciences, clinical research, or regulatory domains is acceptable.
Technical & Functional Skills:
Strong proficiency in Microsoft Office tools (Excel, Word, PowerPoint).
Basic understanding of drug development, clinical research, or clinical science.
Soft Skills:
Excellent organizational and time management skills.
High attention to detail and quality orientation.
Strong written and verbal communication skills.
Ability to work independently and collaboratively in a global team environment.
Strong intercultural awareness with a global perspective.
What Xogene Offers
Structured mentorship from industry experts working at the intersection of AI, regulatory science, and business strategy.
Clear career progression pathways with increasing responsibility as skills and expertise develop.
Exposure to cutting-edge AI technologies, including large language models (LLMs) and conversational systems.
Competitive compensation package with comprehensive benefits.
A results-driven, meritocratic culture that values innovation, accountability, and professional excellence.
Flexible hybrid work environment supporting work-life balance.
Why Join Xogene?
At Xogene, you will contribute to meaningful work that directly impacts clinical trial transparency and patient trust worldwide. This role provides a unique opportunity to build a strong foundation in regulatory compliance while working alongside experts shaping the future of AI-enabled clinical research.
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