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Ctt Specialist - I (Post Graduates - 2026 Passouts)

Xogene
xogene
0-1 years
preferred by company
10 Jan. 2, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Trial Transparency (CTT) Specialist – I (Postgraduates 2026)

Location: Gurgaon, Haryana, India (Hybrid)
Job Type: Full-Time
Category: Clinical Research / Regulatory Affairs
Experience Required: Fresh graduates / 0–1 year relevant experience
Job ID: [Insert ID]


About Xogene

Xogene is transforming clinical trial transparency through AI-powered solutions, helping leading pharmaceutical and life sciences companies achieve regulatory compliance efficiently. By combining regulatory expertise, technological innovation, and advanced AI, Xogene streamlines workflows, accelerates data transformation, and ensures accurate clinical trial disclosure across global regulatory frameworks.

Join Xogene to work in a fast-paced, dynamic environment, gaining exposure to cutting-edge AI technologies, regulatory intelligence, and global clinical trial compliance.


Position Overview

As a CTT Specialist – I, you will be part of Xogene’s Clinical Trial Transparency Team, supporting data entry, document management, and regulatory compliance activities. This entry-level role is ideal for postgraduates graduating in 2026 who have a keen interest in life sciences, clinical research, and regulatory affairs. You will collaborate with analysts, specialists, and managers to ensure high-quality clinical trial registry submissions, plain language summaries, and document redaction.

This role also offers exposure to AI-enabled platforms and allows you to contribute subject matter expertise to technology development projects supporting clinical trial transparency.


Key Responsibilities

  • Enter and manage clinical trial data in global registry systems while ensuring accuracy and compliance.

  • Support document review and quality checks to maintain high data integrity.

  • Author plain language summaries and assist with the redaction/anonymization of clinical and non-clinical documents.

  • Collaborate with Disclosure Coordinators and clients to track project status and meet deadlines.

  • Research, interpret, and apply global regulatory requirements for clinical trial transparency.

  • Provide subject matter input to technology teams to improve AI systems for regulatory compliance.

  • Proactively manage deliverable timelines and communicate risks or delays to project coordinators.

  • Assist with maintaining US and international clinical trial registry postings.

  • Contribute to process improvement initiatives and provide constructive feedback to team members.


Required Qualifications & Skills

  • Postgraduate students completing studies in 2026 (Master’s in Life Sciences or related discipline).

  • Strong interest in clinical research, drug development, and regulatory affairs.

  • Excellent organizational, time management, and self-starter skills.

  • Meticulous attention to detail with high accuracy in data entry and document review.

  • Strong proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).

  • Excellent written and verbal communication skills.

  • Ability to work collaboratively in a team-oriented, intercultural environment.

  • Knowledge of drug development, clinical science, or regulatory processes is a plus.


Experience

  • Fresh graduates / postgraduates with 0–1 year relevant experience in clinical research, regulatory affairs, or life sciences.

  • Bachelor’s degree or equivalent experience in life sciences is preferred.


What We Offer

  • Mentorship from industry experts working at the intersection of AI and regulatory compliance.

  • Exposure to advanced AI technologies, including LLMs and conversational systems.

  • Structured career progression with increasing responsibility as skills develop.

  • Competitive compensation and benefits package.

  • Dynamic, results-oriented culture that values innovation, professional excellence, and accountability.