As a Scientific & Medical Writing Manager, you will implement the operational strategy defined with the Head of Scientific Writing, tracking milestones and deliverables to manage the performance of the Scientific Writing team, ensuring consistency, regulatory compliance and the quality…
The purpose of the role of the Transparency Specialist is to coordinate the delivery of activities related to clinical trial data disclosure in GSK RD in the respective therapy area (Oncology, General Medicines, Specialty, Vaccines) The role is responsible to…
1. As an ADULT VACCINE SPECIALIST you will be responsible for identifying and onboarding a minimum of 40 60 high end HCP s (private clinics) as VACCINATORS (HCP controls Vx journey of patients) by April 2023 and continue to expand…
Provide support for Central Safety Department (CSD) literature screening activities for both ICSR and signal detection purposes in accordance with their procedures and regulatory requirements Support SERM product specialists by identifying articles of interest for relevant safety information from screened…
The purpose of the role of the Transparency Specialist is to coordinate the delivery of activities related to clinical trial data disclosure in GSK R&D in the respective therapy area (Oncology, General Medicines, Specialty, Vaccines). The role is responsible to…
The purpose of the Technical Assurance Manager WREF is to ensure the consistent and sustained performance of engineering systems across WREF through the implementation of a technical assurance framework covering relevant legal, regulatory, safety, operational and strategic risks. Responsibilities include…
The role reports to Experience Design & Channel Orchestrator Lead and the Grade of the Job will be 7/8 The person will act in an individual contributor capacity Primary Duties & Responsibilities: Campaign User Journey Design & Execution Designs well…
Creates & manages a unified HCP view by consolidating and analyzing data from various sources to drive business decisions and improve customer engagement Understands customer experience management and provides relevant insights in order to deliver a meaningful and consistent CX…
Broad scientific/ pharmaceutical industry background with 4 6 years of experience in clinical research and/or in pharmaceutical industry. At least 4 years of professional experience as a plain language writer / editor / scientific / regulatory writer within a professional…
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Organise Joint Planning Sessions with regions and priority markets and collate outputs. Synthesise the outputs of these sessions…
Responsibilities: Providing statistical input to the design, analysis, reporting and interpretation of clinical studies and contribution to publications Identifying, developing and implementing novel statistical methodologies in support of medicine development Influencing clinical development plans, regulatory and commercial strategies. Building and…
The role of the Retrofit Project Associate is to ensure that proposed retrofit changes to ERP template are assessed for any people, process or technology impacts, and where identified, that sufficient consideration has been made to ensure that end users…
As a Medical Writing Asset Lead, you will lead therapy area specific medical writing projects or programs as appropriate in support of the clinical strategy to meet business and regulatory needs, and potentially leading projects across products This role will…
Education required: 1st year students of flagship MBA or specified Programs from specific Institutes in India. Note: This application is open to Selected Institutes only. Your application to the Program will be subject to our engagement confirmation for placement process…