Apply for Novartis Hiring for Associate Clinical Study Manager in Hyderabad. Explore clinical research jobs and build your global pharma career.
Introduction
Novartis, one of the world’s most respected names in the pharmaceutical and healthcare industry, is hiring for the position of Associate Clinical Study Manager in Hyderabad, India. This full-time, hybrid role offers an exceptional opportunity to contribute to life-changing clinical research that directly impacts patient outcomes worldwide. Novartis Hiring for Associate Clinical Study Manager
As part of the Novartis Clinical Operations team, you’ll play a crucial role in planning, executing, and managing clinical studies. This position is ideal for professionals with experience in clinical research, trial management, and project coordination who want to grow in a dynamic, innovation-driven environment.
If you’re passionate about ensuring excellence in clinical trials and wish to work for a global organization dedicated to improving human health, this is your chance to join one of the industry leaders. Novartis Hiring for Associate Clinical Study Manager
About Novartis
Novartis International AG, headquartered in Switzerland, is a global healthcare company that aims to reimagine medicine and improve people’s lives. With a presence in over 150 countries, Novartis develops innovative medicines across oncology, immunology, neuroscience, and cardiovascular therapy areas. Novartis Hiring for Associate Clinical Study Manager
Novartis invests heavily in clinical research, ensuring that each study meets global ethical standards, regulatory compliance, and scientific excellence. Its Hyderabad operations center plays a critical role in managing clinical trials, regulatory documentation, and medical information processes. Novartis Hiring for Associate Clinical Study Manager
By joining Novartis, you’ll become part of a company that values diversity, integrity, scientific rigor, and a passion for patient-centric innovation.
Position Overview: Associate Clinical Study Manager
The Associate Clinical Study Manager is a key member of the Global Drug Development (GDD) organization at Novartis. In this role, you will support the planning, tracking, and reporting of clinical studies from initiation to close-out. You will coordinate with global study teams, vendors, and external partners to ensure that trials are conducted according to Good Clinical Practice (GCP) and regulatory requirements. Novartis Hiring for Associate Clinical Study Manager
This role combines clinical operations management, project coordination, and financial oversight, providing a comprehensive view of global clinical research. Novartis Hiring for Associate Clinical Study Manager
Key Responsibilities
As an Associate Clinical Study Manager at Novartis, you’ll have a diverse range of responsibilities focused on study management, documentation, and operational support. Novartis Hiring for Associate Clinical Study Manager
Your main duties include:
- Clinical Trial Systems Management:
Maintain and update Clinical Trial Management Systems (CTMS) and Trial Master File (TMF) to ensure compliance, accuracy, and audit readiness. - Budget Tracking and Reporting:
Assist in planning, forecasting, and tracking clinical study budgets. Support cost reconciliation and financial reporting activities to ensure fiscal accountability. - Study Progress Monitoring:
Track the progress of ongoing studies and escalate operational challenges to senior study leads. Support issue resolution in collaboration with external service providers. - Meeting Coordination:
Organize and facilitate study-related meetings, prepare documentation, and maintain consistent communication between internal and external stakeholders. - Process Improvement:
Identify opportunities to streamline workflows, enhance efficiency, and implement process improvement initiatives across clinical operations. - Compliance & Documentation:
Ensure all trial documents adhere to Good Clinical Practice (GCP) guidelines, standard operating procedures (SOPs), and global clinical development regulations. - Collaboration:
Work closely with cross-functional teams such as data management, regulatory affairs, and clinical operations to ensure successful study delivery.
Essential Requirements
To qualify for the Associate Clinical Study Manager position, candidates must meet the following requirements: Novartis Hiring for Associate Clinical Study Manager
- Education:
- Bachelor’s degree or higher in Life Sciences, Pharmacy, Nursing, or equivalent scientific discipline.
- Experience:
- Minimum 3 years of experience in clinical operations, project management, or clinical research within the pharmaceutical or CRO industry.
- Technical Knowledge:
- Strong understanding of Good Clinical Practice (GCP), clinical development processes, and trial lifecycle management.
- Familiarity with CTMS, TMF, and other regulatory documentation systems.
- Skills:
- Excellent communication (written and verbal) and interpersonal skills.
- Proven ability to work independently and escalate issues effectively.
- Good organizational and analytical abilities.
- Attention to detail and commitment to quality standards.
- Language Proficiency:
- Fluent in English, both oral and written.
Desirable Requirements
While not mandatory, the following qualifications are highly desirable for candidates aiming to stand out: Novartis Hiring for Associate Clinical Study Manager
- Experience in financial forecasting, budget tracking, and cost reconciliation for clinical studies.
- Prior exposure to global clinical trials or multi-country study management.
- Knowledge of regulatory submission processes and clinical documentation standards.
- Certification in Clinical Research, Project Management, or related fields.
- Experience with vendor coordination and external study partners.
Desired Skills and Competencies
- Clinical Trials Expertise: Understanding of clinical trial phases (I–IV), trial design, and study execution.
- Conflict Management: Ability to manage and resolve issues constructively across global teams.
- Contract Management: Familiarity with vendor contracts and service agreements.
- Effective Communication: Skilled at articulating study objectives and expectations clearly to stakeholders.
- Financial Analysis: Competence in reviewing study budgets and managing cost efficiency.
- Negotiation Skills: Ability to negotiate timelines, deliverables, and budgets with third-party vendors.
Work Location and Type
- Location: Hyderabad, India
- Work Type: Full-time, Hybrid (minimum 3 days per week in office as per Novartis hybrid model)
- Job Requisition ID: REQ-10063488
The hybrid work model allows flexibility while maintaining strong collaboration among cross-functional teams. Employees enjoy the benefits of remote work combined with the advantages of in-person communication and teamwork. Novartis Hiring for Associate Clinical Study Manager
Why Join Novartis
Working at Novartis is more than just a career choice—it’s a commitment to improving global health and transforming the future of medicine. Here’s what makes Novartis an ideal workplace: Novartis Hiring for Associate Clinical Study Manager
- Global Impact: Contribute to life-changing medicines and therapies that reach millions of patients worldwide.
- Career Growth: Access world-class training, mentorship, and professional development programs.
- Innovation Culture: Work in an environment that fosters creativity, research excellence, and scientific exploration.
- Work-Life Balance: Flexible work arrangements, wellness programs, and a supportive work environment.
- Inclusive Workplace: Novartis celebrates diversity, equality, and inclusion—ensuring all employees feel valued and respected.
Equal Opportunity Statement
Novartis embraces diversity and equality of opportunity. The company is committed to building an inclusive workplace that represents a wide range of backgrounds and perspectives. All qualified candidates are encouraged to apply, regardless of gender, ethnicity, or disability.
How to Apply
Interested and eligible candidates can apply online for the Associate Clinical Study Manager – Novartis Hyderabad position through the official Novartis Careers Portal.
Step-by-Step Application Process:
- Visit the official Novartis Careers website: https://www.novartis.com/careers
- In the search bar, type “Associate Clinical Study Manager”.
- Select the job location as Hyderabad, India.
- Click on the listing titled “Associate Clinical Study Manager – REQ-10063488”.
- Read the job description thoroughly.
- Click on “Apply Now” to start your online application.
- Create or log in to your Novartis Careers account.
- Upload your updated resume and complete the application form.
- Submit your application before November 8, 2025.
Key Details at a Glance
- Company: Novartis
- Position: Associate Clinical Study Manager
- Location: Hyderabad (Hybrid)
- Job Type: Full-Time
- Experience Required: Minimum 3 years
- Application Deadline: November 8, 2025
Conclusion
The Associate Clinical Study Manager role at Novartis, Hyderabad, is a gateway to a fulfilling and impactful career in clinical research and drug development. This position offers a perfect balance between operational responsibility and scientific contribution, making it ideal for candidates seeking long-term growth in the pharmaceutical sector. Novartis Hiring for Associate Clinical Study Manager
By joining Novartis, you’ll not only gain professional experience in managing global clinical trials but also contribute to a purpose-driven mission—reimagining medicine and improving lives worldwide. Novartis Hiring for Associate Clinical Study Manager
If you’re ready to make a difference and build a career with one of the world’s most trusted pharmaceutical organizations, apply now and take the next step in your journey with Novartis.
For verified pharma job updates, visit PharmaJobHub.in – India’s trusted pharma career portal.
Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.
