Job Update: Graduates Vacancy at GSK

Overview:

GSK is hiring an experienced Associate Director Study Delivery Management at their Bengaluru location. As a Clinical Study Manager, you will be responsible for leading Global In-Country Clinical operations teams to improve quality processes and evolve the ways of working to optimise clinical operations and foster stronger quality relationships with the sites. You will also support the Director of Quality, Training and Capability Development with all required activities to achieve business goals.

The complete details of this job are as follows:-

Roles and Responsibilities:

The Ideal Candidate should be able to:

Lead and participate in cross functional teams to assess transformational initiatives and tools to help simplify ways of working and accelerate portfolio delivery

Identify future capability and competency requirements in line with R&D strategy and the constantly changing and evolving internal and external environment

Support capability development globally across the Local Operating Countries (LOCs) in partnership with the Regional Directors and LOC Clinical Operational Heads

Sponsor and oversee the different communities across the Global In-Country Clinical Operations Team to ensure alignment between the communities and that the activities to bring simplification and value to the business

Foster a culture of simplification, standardisation, sharing best practices, working across boundaries and continuous improvement through a variety of mechanisms

Develop and drive the implementation of the risk register and management monitoring templates to each LOC and continuously look for opportunities to simplify and evolve management monitoring activities to the next level

Conduct regular holistic quality discussions with the LOCs based on collective intelligence in partnership with the Regional Directors

Partner with various business areas to analyse the global management monitoring output looking for local, regional, and global trends and share those learnings with the LOCs

Support the Director of Quality, Training and Capability Development to build an effective Quality Management System (QMS) in partnership with other business areas

Work with Clinical Quality Assurance (CQA) to support and where possible facilitate regulatory inspections, identify root causes for findings, and identify appropriate corrective and preventative actions; Ensure these learnings are shared with the business.

The Ideal Candidate should also have:

Master’s Degree in science related field

Advanced knowledge of the drug development processes and key operational interfaces

Ability to plan, manage and lead cross-functional projects

Excellent communication skills and able to explain complex situations

Eligibility:

Bachelor’s Degree

5 or more than years of experience developing quality programs for clinical operations

Experience with Good Clinical Practices (GCP) and International Council for Harmonization (ICH) guidelines

Experience working across geographies with clinical and corporate governance principals

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