Director Clinical Process Excellence at Sandoz

, Telangana, India -

Full Time

Start Date

Immediate

Expiry Date

02 Oct, 26

Salary

0.0

Posted On

04 Jul, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Clinical Trials, People Management, Program Management, Regulatory Compliance, Resource Management, Risk Management, Process Governance, Quality Management System, Change Management, Stakeholder Management, Strategic Thinking, Audit Management, GCP, Clinical Operations, Knowledge Management

Industry

Pharmaceutical Manufacturing

Description

Job Description Summary Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. Join us, the future is ours to shape! Accountable to lead the design, governance, and continuous optimization of clinical process frameworks and quality systems for clinical development, ensuring efficient management of SOPs, templates, regulatory intelligence, training, audits, and operational processes; drive standardization, compliance, and cross-functional collaboration to support high-quality clinical execution and sustainable operational excellence. Job Description Major accountabilities: Process Governance & Standardization: Establish and oversee robust clinical process governance frameworks, including management of process forums, SOP systems, and standardized templates to ensure consistency and efficiency across clinical operations. Quality System Management: Lead the development, maintenance, and continuous improvement of the Quality Management System (QMS), ensuring alignment with regulatory requirements and organizational standards. Documentation & Knowledge Management: Ensure effective management of clinical documentation, including SOP master lists, eTMF templates, SharePoint systems, and archival processes, to support compliance, traceability, and accessibility. Regulatory Intelligence & Compliance Oversight: Drive regulatory intelligence gathering and assessment, translating insights into actionable process improvements and ensuring ongoing compliance with evolving regulations. Training & Capability Building: Oversee clinical training strategy and delivery (including GCP and process training), ensuring workforce capability, compliance, and continuous skill development. Audit, Inspection & Continuous Improvement: Lead/ support internal audits (as per assignment), self-inspections, and quality investigations (including CAPA coordination), driving remediation actions and embedding a culture of continuous improvement and inspection readiness. Cross-functional Collaboration & Operational Support: Partner with Legal, Data Privacy, Medical Affairs, and other stakeholders to ensure integrated process execution, while supporting key administrative and operational activities such as onboarding, organizational governance, and system transitions. Minimum Requirements: Work Experience: 13+ years pharmaceutical industry clinical experience in Development and Clinical Operations Excellent leadership, communication (written/verbal), stakeholders’ management and collaboration skills Excellent organizational skills, with the ability to prioritize/work effectively in a changing environment Extensive experience in conducting a wide range of study types and the end-to-end clinical process Experience in people management and development across countries with the ability to energize others around purpose/impact Strong interpersonal, problem-solving, change management and negotiation skills Displays strategic thinking, an innovative mindset and a solutions-oriented approach Experience in a global environment with the ability to lead cross functional, multi-cultural teams Ability to work independently and create innovative solutions with little direction Why Sandoz? Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more! With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably. Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is supported! Join us! Skills Desired Clinical Research, Clinical Trials, People Management, Program Management, Regulatory Compliance, Resource Management (Organizational), Risk Management Our Purpose here at Sandoz is pioneering access for patients. As the global leader in 'off-patent' high quality medicines, we are able to make medicine more affordable and accessible. Our broad global portfolio comprises of approximately 1,300 quality biosimilar and generic medicines, enabling us to provide more than 900 million patient treatments across 100+ countries per year, and while we are proud of this achievement, we have an ambition to do more! Powered by our talented and ambitious colleagues, who, in return for dedication and skills, experience a flexible, collaborative & inclusive culture where diversity of thought is welcomed and where personal growth is nurtured!

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

Lead the design, governance, and optimization of clinical process frameworks and quality systems to ensure efficient clinical development. Drive standardization, regulatory compliance, and cross-functional collaboration to support high-quality clinical execution.