Xogene CTT Specialist I (Clinical Trial Transparency) Jobs – Post Graduates 2026 | Gurgaon

Xogene hiring CTT Specialist I in Gurgaon. Post Graduates 2026 pass-outs eligible. Clinical trial transparency role.

Xogene is hiring CTT Specialist – I (Clinical Trial Transparency) for its growing team in Gurgaon, Haryana. This opportunity is specifically targeted at post‑graduate students completing their degree in 2026 who want to start a career at the intersection of clinical research, regulatory compliance, and AI‑driven healthcare technology. The role offers early exposure to global clinical trial disclosure requirements, regulatory intelligence, and real‑world transparency operations for leading pharmaceutical and life sciences companies.

This position is ideal for candidates who are detail‑oriented, curious about drug development and clinical science, and motivated to work in a fast‑growing, technology‑focused organization shaping the future of clinical trial transparency.

Company Overview

Xogene is a specialized life sciences technology company focused on transforming clinical trial transparency through AI‑powered and agentic solutions. The company combines deep regulatory expertise with advanced automation to help pharmaceutical, biotechnology, and life sciences organizations meet global clinical trial disclosure and compliance requirements efficiently.

Xogene works across global regulatory frameworks, supporting protocol registrations, results disclosure, plain language summaries, document anonymization, redaction, and regulatory intelligence. Its solutions streamline complex transparency workflows while maintaining strict compliance with evolving global regulations.

As a fast‑growing and merit‑driven organization, Xogene offers a professional environment where innovation, accountability, and continuous learning are valued. Employees gain exposure to cutting‑edge AI technologies while contributing directly to ethical research practices and patient‑centric transparency.

Job Role & Responsibilities

The CTT Specialist – I role supports clinical trial transparency operations across global and regional disclosure activities. The position involves structured data handling, document review, regulatory research, and collaboration with both clients and internal technology teams.

Key Responsibilities

• Support the Clinical Trial Transparency (CTT) team with data entry activities for assigned clinical studies.
• Enter clinical trial data directly into applicable global and regional registry systems.
• Communicate regularly with internal CTT team members to ensure timelines and deliverables are met.
• Perform quality checks by reviewing documents and entered data with strong attention to detail.
• Support redaction and anonymization of clinical and non‑clinical documents to protect confidential and personal information.
• Author plain language summaries for clinical trial disclosures.
• Track study status and coordinate with client‑side Disclosure Coordinators when required.
• Develop subject matter expertise in clinical trial transparency by researching, interpreting, and applying global regulatory requirements.
• Support AI and technology enablement initiatives by acting as a subject matter expert for clinical trial transparency.
• Proactively manage timelines and flag risks to project coordinators and management.
• Support administrative maintenance of US and international clinical trial registry postings.
• Contribute to continuous process improvement and provide constructive feedback within the project team.

This role builds a strong foundation in regulatory compliance, transparency operations, and technology‑enabled clinical research support.

Eligibility / Qualifications

Required Education

Candidates must meet one of the following criteria:

• Master’s degree students completing post‑graduation in 2026
• Bachelor’s degree with strong interest in life sciences or clinical research
• Two years of commensurate experience may be considered

Skills & Competencies

• Strong interest in life sciences, clinical research, and regulatory compliance
• Excellent organizational and time‑management skills
• High attention to detail and data accuracy
• Strong proficiency in Microsoft Office tools including Excel, Word, and PowerPoint
• Effective written and verbal communication skills
• Ability to work collaboratively in cross‑functional and multicultural teams
• Basic knowledge of drug development or clinical science is an advantage

Location & Salary

Work Mode: Hybrid
Job Location: Gurgaon, Haryana, India

Application Process

Eligible candidates should apply through the official Xogene careers portal using the link below.

Apply Online:

Applicants are advised to apply only through the official link. Xogene does not charge any fees during the recruitment or selection process.

Frequently Asked Questions (FAQs)

Who can apply for the CTT Specialist – I role?

Post‑graduate students completing their degree in 2026 with a strong interest in life sciences and clinical research are eligible to apply.

Is this role suitable for freshers?

Yes. This role is designed for fresh post‑graduates and early‑career professionals seeking entry into clinical research and regulatory compliance.

What type of work does clinical trial transparency involve?

It includes registry data entry, document review, regulatory research, redaction, anonymization, and authoring of plain language summaries.

Is this a technology‑focused role?

Yes. The role involves collaboration with AI and technology teams to support clinical trial transparency solutions.

Where is the job located?

The position is based in Gurgaon, Haryana, with a hybrid working model.

Summary Table