As a Clinical Data Scientist, you will be responsible for overseeing the end-to-end DS&M study related activities and is accountable for all Data Strategy & Management (DS&M) study deliverables in terms of quality & delivery to plan.,

Accountable for the end-to-end DS&M study related activities in terms of quality & delivery to plan which include:
For an in-house study, leads the day-to-day DS&M operational study related activities, acts as a member of the study core team and is the single point of contact for all the DM study related activities & matters
For study outsourced through a DM Functional Service Provider (FSP), conducts & documents DM sponsor oversight of the end-to-end FSP study related activities and ensures training on the protocol to the FSP resources working on the study. May oversee Full Service Outsourced (FSO) studies.
Provides DM operational input into the study design, the protocol, study planning, study documents including the studyrisk register
Provides reports, status updates, feedback and advice to key study stakeholders on study progress
Creates or reviews study level timelines for DM deliverables and ensures teams adhere to these
Promotes the implementation of clinical data standards to increase consistency, efficiency & productivity
Acts as the first point of escalation for all DM study issues. Understands, mediates and solves issues related to DM study deliverables and escalates as required to DM representative at Asset level
Ensures DM study deliverables are in compliance with GSK SOPs and regulatory guidelines, We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.

Bachelor's Degree, in scientific or business discipline
Experienced in Clinical Data Management processes, standards and clinical systems
Project Management
Exposure to InForm, Rave/ Veeva/ OC, e-Diaries, e-Source is an added advantage
Proficient in Microsoft exce and validation methodology
Basic knowledge of PL SQL, SAS is an added advantage
Understanding of general data flow & database architecture concepts
Good understanding of regulations including ICH-GCP, 21 CRF part 11, CDISC requirement
Comprehensive understanding of clinical drug /Vaccine development process
Knowledge of medical terminology, anatomy and physiology
Proven ability to prioritize and multi-task, along with effective time management skills Detail oriented, organized
Excellent interpersonal and teamwork skills
Demonstrates adaptability and an agile mindset
Problem solving mindset
Quick learner
Results oriented and customer focused
Willing to work in a Global environment

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people over the next 10 years. R&D is committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease. Science and technology are coming together in a way they never have before, and we have strong tech-enabled capabilities that allow us to build a deeper understanding of the patient, human biology and disease mechanisms, and transform medical discovery. We are revolutionising the way we do R&D. We're uniting science, technology and talent to get ahead of disease together.