Apply for Analyst Clinical Label Management Jobs in Hyderabad at Novartis. Full-time role supporting clinical trial labeling operations.
About the Company
Novartis is a leading global healthcare company committed to reimagining medicine to improve and extend people’s lives. With a strong presence across research, development, manufacturing, and clinical operations, Novartis focuses on delivering innovative therapies that address some of the most complex health challenges worldwide. Analyst Clinical Label Management Jobs
The organization operates with a strong emphasis on quality, compliance, patient safety, and ethical standards. Novartis fosters a culture of integrity, accountability, collaboration, and continuous improvement. Employees are encouraged to contribute ideas, develop leadership capabilities, and grow within a structured yet flexible professional environment.
Working at Novartis means being part of a globally respected organization where operational excellence, compliance, and scientific rigor play a critical role in every clinical and commercial activity.
Job Details
- Job Title: Analyst – Clinical Label Management
- Company: Novartis
- Job Requisition ID: REQ-10070942
- Location: Hyderabad (Office-based)
- Employment Type: Full-Time
- Department: Clinical Trial Supply / Label Management
- Application Deadline: February 28, 2026
- Time Left to Apply: 23 Days
This role is ideal for professionals with experience in pharmaceutical or clinical trial environments who want to specialize in clinical labeling operations and compliance. Analyst Clinical Label Management Jobs
Job Description
The Analyst – Clinical Label Management is responsible for executing label design, review, and related activities in alignment with the labeling strategy defined by the Label Lead and established organizational processes. This position plays a key role in ensuring accurate, compliant, and timely delivery of labeling activities that support global clinical trials. Analyst Clinical Label Management Jobs
The role requires close coordination with internal stakeholders such as Clinical Trial Supply Managers and Supply Chain teams, as well as external service providers for specialized labeling requirements. The analyst ensures that labeling documentation meets quality standards, regulatory expectations, and internal compliance requirements.
This position demands a strong understanding of GMP principles, attention to detail, and the ability to manage multiple labeling activities simultaneously while maintaining transparency and consistent reporting. Analyst Clinical Label Management Jobs
Skills / Qualifications
Candidates applying for the Analyst – Clinical Label Management position should meet the following educational and professional criteria.
Educational Qualifications
- Degree in Science, Engineering, or an equivalent discipline
- Apprenticeship or formal education in a logistical, technical, or related business area is desirable
Work Experience Requirements
- More than 2 years of practical experience in the chemical or pharmaceutical industry
OR - More than 3 years of experience in the relevant field of expertise
Analyst Clinical Label Management Jobs
Technical and Functional Skills
- Strong knowledge of GMP standards and pharmaceutical compliance
- Understanding of Health, Safety, and Environment (HSE) requirements
- Familiarity with clinical trial supply and labeling processes
- Working knowledge of SAP ERP and master data management
- Exposure to logistics, warehouse management, and supply chain operations
- Ability to manage documentation repositories and labeling templates
Analyst Clinical Label Management Jobs
Professional and Behavioral Skills
- Good organizational, planning, and time-management skills
- Strong problem-solving and analytical thinking abilities
- Effective communication, negotiation, and interpersonal skills
- Ability to work efficiently in interdisciplinary and cross-functional teams
- Fundamental leadership and presentation skills
- Capability to operate in a structured, quality-driven environment
Analyst Clinical Label Management Jobs
Key Responsibilities
As an Analyst – Clinical Label Management, you will be responsible for executing and supporting a wide range of labeling activities essential to clinical trial operations. Analyst Clinical Label Management Jobs
Key responsibilities include:
- Generation of labels for Investigational Medicinal Products (IMP)
- Preparation and management of randomization lists and randomization schedules
- Ensuring agreed milestones, quality standards, and timelines are consistently met
- Designing labels based on strategic inputs and specific clinical study requirements
- Acknowledging and managing ticket assignments promptly to maintain workflow continuity
- Uploading study-related forms, Study Label Templates (SLTs), and supporting documentation into relevant repositories accurately
- Providing regular progress updates and issue escalation to the Label Lead
- Maintaining consistent and transparent status reporting for all assigned activities
- Ensuring label compliance with study design, pack design, and analytical specifications of the IMP
- Verifying compliance with country-specific Health Authority requirements and internal Novartis compliance standards
- Maintaining and updating the Phrase Library, including validated country-specific regulatory phrases and translations
- Performing GMP line unit checks (LU1b) for labels when certified and required, in accordance with SOPs
- Documenting GMP checks accurately and reporting quality events, deviations, or non–Right First Time (RFT) cases to the Team Head or Deputy
- Coordinating effectively with internal stakeholders such as Clinical Trial Supply Managers and Supply Chain Managers
- Collaborating with external label service providers for specialized labeling requirements
- Supporting inspections by explaining labeling processes clearly during internal and external audits
- Participating actively in projects, internal networks, and professional forums
- Ensuring execution of all assigned tasks according to defined quality, quantity, and timeline expectations
- Adhering strictly to established processes, procedures, and Novartis values and behaviors
Analyst Clinical Label Management Jobs
Benefits / Perks
Novartis offers a professional environment designed to support employee growth, compliance excellence, and long-term career development. Analyst Clinical Label Management Jobs
Benefits and perks include:
- Opportunity to work with a global pharmaceutical leader
- Exposure to international clinical trial labeling and regulatory requirements
- Structured training and certification opportunities
- Collaborative, inclusive, and quality-driven work culture
- Career development pathways within clinical operations and supply chain functions
- Strong focus on compliance, safety, and ethical practices
- Stable full-time employment with long-term growth potential
Why You Should Join
Joining Novartis as an Analyst – Clinical Label Management provides a unique opportunity to build deep expertise in clinical trial labeling, regulatory compliance, and GMP-driven operations. This role allows you to work at the intersection of clinical research, supply chain management, and regulatory affairs. Analyst Clinical Label Management Jobs
You will gain hands-on exposure to global clinical trials, collaborate with cross-functional teams, and develop skills that are highly valued across the pharmaceutical industry. The position offers a solid foundation for advancing into senior labeling, clinical supply, or quality compliance roles in the future.
For professionals who value precision, compliance, structured processes, and continuous learning, this role offers an excellent platform for long-term career growth. Analyst Clinical Label Management Jobs
FAQs
Q1. Is this role office-based or remote?
This is a full-time, office-based role located in Hyderabad.
Q2. What type of experience is required for this position?
Candidates should have at least 2 years of pharmaceutical industry experience or 3 years in a relevant field.
Q3. Is GMP knowledge mandatory?
Yes, good knowledge of GMP standards and processes is essential for this role.
Q4. Will this role involve inspections or audits?
Yes, the role requires participation in internal and external inspections related to labeling processes.
Q5. Is SAP knowledge required?
Working knowledge of SAP ERP and related systems is highly desirable.
How to Apply
Interested and eligible candidates can apply directly through the official Novartis careers portal using the job requisition ID REQ-10070942 or via the platform where this job vacancy is listed. Applicants should submit an updated resume highlighting relevant experience in clinical labeling, GMP compliance, and pharmaceutical operations.
Early application is recommended, as applications will be reviewed on a rolling basis until the closing date of February 28, 2026. Analyst Clinical Label Management Jobs
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