Regulatory Data Content Specialist Pharma Jobs at Roche in Chennai Hyderabad for clinical trial disclosure and regulatory affairs professionals.
Company Overview
Roche is a globally respected healthcare organization committed to advancing science and improving access to innovative medicines and diagnostics. With a strong focus on patient-centricity, Roche operates across pharmaceuticals and diagnostics, supporting millions of patients worldwide. In India, Roche Services & Solutions plays a key role in delivering high-quality global business and regulatory services that enable innovation, compliance, and operational excellence across the product lifecycle. Regulatory Data Content Specialist Pharma Jobs
Job Location & Employment Type
- Job Locations: Chennai, Tamil Nadu / Hyderabad, Telangana
- Employment Type: Full-Time (Permanent)
- Work Mode: Office-based / Hybrid (as per business requirements)
- Functional Area: Regulatory Affairs | Regulatory Data & Content | Clinical Trial Disclosures
Open Positions / Department Details
- Position: Regulatory Data & Content Specialist – Disclosures
- Business Unit: Roche Services & Solutions (RSS)
- Department: Pharma Development Regulatory (PDR) – Innovation & Sustainment
- Job ID: 202602-102886
This role is part of a global regulatory capability team responsible for strengthening regulatory data quality, transparency, and compliance across clinical development programs. Regulatory Data Content Specialist Pharma Jobs
Key Roles & Responsibilities
As a Regulatory Data & Content Specialist – Disclosures, the selected candidate will contribute to global clinical trial transparency and regulatory disclosure activities. The role involves close collaboration with regulatory, clinical, and cross-functional teams to ensure accurate and timely public disclosure of clinical trial information. Regulatory Data Content Specialist Pharma Jobs
Core Responsibilities
- Act as a subject matter expert in the pharmaceutical product development lifecycle, with a strong focus on regulatory and disclosure-related activities.
- Develop and maintain a clear understanding of global clinical development pathways and regulatory requirements governing clinical trial disclosures.
- Support the posting of clinical trial protocols, registrations, and results on public disclosure platforms such as ClinicalTrials.gov and the EU Clinical Trial Results Registry.
- Identify clinical studies requiring registration or results disclosure and ensure relevant stakeholders are informed of regulatory timelines and obligations.
- Coordinate with global project teams, affiliates, and functional partners to ensure awareness and compliance with clinical trial disclosure responsibilities.
- Submit protocol-related documents for registry postings and perform quality control checks to ensure consistency, accuracy, and regulatory compliance.
- Work closely with cross-functional stakeholders to gather required data, approvals, and confirmations needed for timely disclosure submissions.
- Monitor disclosure workflows and track progress to ensure registry entries and results postings are completed within regulatory timelines.
- Manage correspondence related to disclosure activities and ensure timely follow-up and resolution of queries from internal teams.
- Maintain high-quality regulatory records and ensure disclosure documentation aligns with internal standards, policies, and external regulations.
- Contribute to continuous improvement initiatives by identifying process gaps and supporting enhancements in regulatory disclosure systems and tools.
Regulatory Data Content Specialist Pharma Jobs
Eligibility Criteria
Education
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Clinical Research, or a related scientific discipline.
- Pharm D candidates are also eligible.
Experience
- Minimum 4+ years of relevant experience in the pharmaceutical or biotechnology industry.
- Hands-on exposure to Regulatory Affairs, Regulatory Writing, or Clinical Trial Disclosure activities is highly preferred.
- Prior experience supporting regulatory or product development functions will be considered an advantage.
Regulatory Data Content Specialist Pharma Jobs
Skills Required
- Solid understanding of drug development processes and familiarity with global regulatory frameworks and guidelines such as GxP, GCP, and ICH.
- Practical knowledge of clinical trial disclosure requirements and public trial registries.
- Strong computer proficiency, including Microsoft Office Suite, Google Workspace (gSuite), and Adobe Acrobat.
- Excellent written and verbal communication skills in English.
- Ability to work effectively in cross-functional, matrix-based global teams with a strong sense of ownership and urgency.
- Strong organizational, documentation, and project planning skills with keen attention to detail.
- Capability to manage multiple tasks, prioritize workload, and meet strict regulatory deadlines.
- Self-motivated, learning-oriented, and quality-focused mindset with an interest in solving complex regulatory challenges.
- Collaborative attitude with a partner-service mindset and adaptability to fast-paced, evolving environments.
Preferred / Good-to-Have
- Certification or formal training in Regulatory Affairs or Clinical Research (e.g., PG Diploma in Clinical Research or Regulatory Affairs).
- Prior experience in regulatory writing or disclosure-related documentation.
Regulatory Data Content Specialist Pharma Jobs
Salary & Benefits
- Salary: As per company norms and role location
- Compensation details may vary based on the primary posting location and will be discussed during the hiring process.
- Employees receive access to a collaborative work culture, learning opportunities, and global exposure within Roche’s regulatory ecosystem.
Selection Process
- Application screening
- Technical and functional interview rounds
- Final HR discussion
The hiring process may differ based on business needs and location.
How to Apply
Interested candidates can apply through the online application process mentioned in the official job posting.
Important Dates
- Application timelines are subject to change.
- Early applications are recommended for better consideration.
Why Apply for This Pharma Job?
This position offers a unique opportunity to work at the intersection of regulatory affairs, clinical development, and data transparency. Professionals will gain exposure to global regulatory disclosure requirements, collaborate with international stakeholders, and contribute directly to patient-centric regulatory compliance. The role is ideal for candidates seeking long-term growth in regulatory data, content management, and clinical trial disclosures within a globally respected healthcare organization. Regulatory Data Content Specialist Pharma Jobs
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform. We are not affiliated with any pharmaceutical company or recruiter. Job details are shared strictly for informational purposes. Candidates are advised to verify all information from official sources before applying. Regulatory Data Content Specialist Pharma Jobs
Final Call-to-Action
If you have experience in regulatory affairs and clinical trial disclosures and want to contribute to global healthcare innovation, apply now and advance your regulatory career. Regulatory Data Content Specialist Pharma Jobs
