Clinical Trial Transparency (CTT) Team Member – Pune
Location: Pune, Maharashtra, India (Hybrid)
Job Type: Full-Time
Category: Clinical Research / Regulatory Affairs
Experience Required: 3–5 years in medical writing or clinical trial transparency
About Xogene
Xogene is a global leader in clinical trial transparency services, combining deep regulatory expertise with AI-powered technology to streamline compliance for pharmaceutical, biotechnology, and life sciences companies. Our advanced, end-to-end platforms simplify clinical trial disclosure, protocol registration, results posting, and patient engagement initiatives.
Joining Xogene means becoming part of a fast-growing, innovative organization that prioritizes professional growth, work-life balance, and meaningful contributions to global health.
Position Overview
As a CTT Team Member, you will support Xogene’s Clinical Trial Transparency (CTT) Team in ensuring accurate, compliant, and timely clinical trial disclosures across global registries. This role involves data entry, document redaction, plain language summary authoring, quality review, and administrative support for US and international clinical trial postings. You will collaborate with specialists, managers, and technology teams to enhance workflow efficiency and contribute subject matter expertise to AI-enabled solutions.
This role is ideal for experienced medical writers or clinical trial professionals who are detail-oriented, organized, and capable of working in a hybrid environment.
Key Responsibilities
Execute clinical trial posting activities for drug, device, and biologic trials across global registries.
Perform redaction and anonymization of clinical and non-clinical documents to ensure confidentiality.
Author plain language summaries to meet regulatory requirements.
Conduct quality checks on documents and data entries to maintain accuracy and compliance.
Manage timelines, track deliverables, and communicate with internal teams and stakeholders.
Record and monitor clinical trial disclosure activities for compliance reporting.
Support administrative tasks related to US and international clinical trial registry postings.
Act as a point of contact for internal and client inquiries related to clinical trial transparency.
Required Qualifications & Skills
Bachelor’s degree in Science or related discipline; Master’s degree preferred.
3–5 years of experience in medical writing, clinical trial transparency, or regulatory affairs.
Strong interest in life sciences, drug development, or clinical research.
Excellent organizational, time management, and multitasking skills; self-starter mindset.
Meticulous attention to detail with high accuracy in data entry and document review.
Proficient in Microsoft Office Suite (Excel, Word, PowerPoint).
Strong written and verbal communication skills.
Collaborative and team-oriented with intercultural understanding and global perspective.
Knowledge of regulatory frameworks and clinical trial processes is a plus.
What Xogene Offers
Mentorship from industry experts bridging AI technology and regulatory compliance.
Exposure to cutting-edge AI tools, including LLMs and conversational systems.
Structured career growth with increasing responsibility as skills develop.
Competitive salary and benefits package.
A results-driven culture that values innovation, professional excellence, and accountabil
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