GSK Recruitment 2023 for Trainee Analyst | M.Pharm/M.Tech/MCA | Bangalore

GSK Recruitment 2023 notification announced for the posts of Trainee Analyst. Candidates with the qualification of  M.Pharm/M.Tech/MCA are eligible to apply. The detailed eligibility and selection process are explained below.

GSK Recruitment 2023 for Trainee Analyst:

Detailed Eligibility:

Trainee Analyst:

• Fresher only.
• Candidates who are currently working or have prior full-time work experience are not eligible.
• Candidates who are currently interning or have prior internship experiences are eligible.
• PharmD students are not eligible
• Education: M.Pharm / M.Tech (Biotechnology) / MCA/ M.Tech Computer Science only.
• Pass out: 2021/2022 / 2023 only.

Key Responsibilities:

• As a trainee Analyst deputed in DS&M sub-functions, at a minimum would carry out the following responsibilities:
• If in the capacity of a Data Management role: End-to-end data review and data cleaning activities on a day-to-day basis for the assigned study/studies.
• If in the capacity of a Data Standards role: Deliver timely and quality reviews of Data Standards and manage standardization activities.
• If in the capacity of an SDTM & Programming role: Ensure timely and quality development, validation, and review of SDTM programs to support study-level conversion of clinical trial data and to ensure various aspects of SDTM activities are thoroughly and accurately conducted.
• If in the capacity of a Coding role: Ensures timely and quality delivery of coded terms, (for Adverse events, concomitant medications, medical histories, medical procedures, etc.) and the effective usage of medical and drug terminology, for clinical trials and other databases as needed across GSK.
• If in the capacity of a Data Acquisition role: Responsible for the technical development of electronic data capture (EDC) and/or Electronic Patient-Reported Outcomes (ePRO) solutions and/or the technical acquisition of vendor data.
• If in the capacity of a Validation role: Ensure various aspects of a clinical study are thoroughly and accurately tested that includes eDC/eCRF rules, User Acceptance Testing (UAT), backend SAS checks, and other non-eDC aspects are validated to company and industry standards.

For any sub-function, the must-have responsibilities will include:

• Engage in activities that enhance automation in a process, involve in tool maintenance and development.
• Apply technical knowledge on a need basis for any of the following – Programming / UAT / Data cleaning & Analysis / Validation / Regulatory submissions.
• Assist in the creation and maintenance of Quality plans and implementation at the study level.
• Ensure all task-related documents are accurate and present in the eTMF system.
• Support activities for process and tool improvement.
• Adhere to the relevant departmental SOPs, corporate policies, regulatory requirements, and industry best practices.
• Compliant in completing all task-related training via LMS and ILT.
• Provides relevant reports, status updates, and feedback on trends observed in day-to-day tasks.
• Contributes to after-action reviews (success or failure) to share learnings and propose improvements for the future.
• Involve in interaction with IT, the Clinical Systems team, and the vendors that are hosting and/or supporting the applications.

About GSK:

• 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 organization where people can thrive.
• Getting ahead means preventing and treating disease, and we aim to positively impact the health of 2.5 billion people by the end of 2030.

How to apply for GSK Recruitment 2023?

Interested and eligible candidates can apply for the job online as soon as possible.

For more details & Apply: Click here

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Reviewed by Prasanth S