Job Description

Site Name: Bengaluru Luxor North Tower Posted Date: Aug 10 2023 As R&D efforts follow science without constraint, we need to take full advantage of our internal data and expertise, as well as leverage external services and technology, to inform, optimize and validate our clinical trial protocols and study delivery plans. This includes the management of a robust site feasibility process. As such we are seeking to appoint a Clinical Operations Planning Analyst to create data driven, high quality insights and modelling to support clinical operations project and study team members. This role will directly support clinical operations planning activities. Key Responsibilities include, but are not limited to: Use internal and industry data sources, along with data analytics, to generate insights used for the planning of clinical trials Utilisation of current and emerging data sources to identify risks and challenges to optimise clinical trial protocol design Lead the site feasibility process in close partnership with the network of local offices Provide timely, high-quality deliverables (e.g. recruitment plans, feasibility report) to clinical trial teams to support the clinical trial planning Actively participate in team meetings to obtain relevant information and present the result of their work Comprehensive tracking of assumptions used to generate deliverables Contribute to the tracking and reporting of KPIs and OKRs Drive continuous improvement in Feasibility and Clinical Operations Planning processes Identify and share trial informatics best practice and exemplars within Clinical Operations. Maintain information on impact and successes. Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: Bachelor\'s degree in relevant field 10+ years relevant industry experience Previous experience in a clinical development operations or study feasibility role at a CRO, pharmaceutical company or other relevant environment Track record in problem solving Knowledge of project management concepts Results orientated with a drive to set and reach challenging goals with high standards for performance Excellent written and verbal communication skills Ability to build strong relationships Ability to analyse data from divergent sources and translate it into meaningful recommendations Understanding of the drug development process Understanding of all relevant industry guidelines (ie FDA, GCP and ICH guidelines) Preferred skills: Master\'s or PhD degree in relevant field Experience utilizing clinical trial recruitment modelling tools Experience utilizing industry clinical trial related data sources (i.e., CiteLine, DQS, TriNetX, etc) Experience across therapeutic areas would be advantageous Experience with data manipulation, visualization, or advanced analytics High level of proficiency with Microsoft Office GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030. Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it\'s also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We\'re committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK\'s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. 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