Trainee Analyst | Bengaluru | GSK

Trainee Analyst | Bengaluru | GSK

Posted 2 weeks ago

About :

Over the last four years, GSK has already delivered unprecedented change, improving R&D, becoming a leader in Consumer Healthcare, strengthening leadership, and transforming commercial execution. It is now implementing the most significant changes to our business in over 20 years. It plans to split into two new companies in 2022: a new GSK with a leading portfolio of vaccines and specialty medicines, as well as R&D based on the immune system and genetics science, and a new world-leading consumer healthcare company with well-known and trusted brands.

New goals necessitate new goals.

Job’s Purpose :

The Trainee Analyst is responsible for learning and applying knowledge/training on the tasks assigned on a daily basis by adhering to related GSK standard operation, guidance, and procedural documents while ensuring quality and delivery within set timelines with minimal supervision.

Job Description :

  • If you are in a Data Management role, you will be responsible for end-to-end data review and cleaning activities on a daily basis for the assigned study/studies.

  • If you are in charge of Data Standards, you must deliver timely and high-quality reviews of Data Standards and manage standardisation activities.

  • If you are in charge of SDTM and programming, you will be responsible for ensuring the timely and quality development, validation, and review of SDTM programmes to support study-level conversion of clinical trial data and ensuring that various aspects of SDTM activities are thoroughly and accurately carried out.

  • If in a Coding role, ensures timely and quality delivery of coded terms (for Adverse events, concomitant medications, medical histories, medical procedures, and so on) as well as the effective use of medical and drug terminology in clinical trials and research.

  • 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 including EDC/eCRF rules, User Acceptance Testing (UAT), backend SAS checks, and other non-EDC aspects are validated to company and industry standards.

Educational Qualifications :

  • Bachelor’s Degree, in a scientific or business discipline

  • Life-science or related medical/clinical area ranging from Fresh Graduates to upto 2 years of Clinical Research or Information Systems or relevant scientific experience and demonstrated good collaboration and communication skills

Soft skills :

  • Detail-oriented, organized, able to grasp information

  • Display interpersonal skills

  • Demonstrate effective communication skills within a matrix environment

  • Team spirit – ability to facilitate interfaces within an extended network

  • Ability to manage priorities within the stipulated timeframe

  • Ability to anticipate changes and be flexible in their implementation

  • A solution-oriented attitude

Hard skills

  • Thorough computer skills, understanding of general data flow & interfaces

  • Awareness of the drug development process and working knowledge of GxP

  • Awareness of converting structured and unstructured data from various sources

  • Ability in developing utility macros

  • Proficient in Microsoft Office tools

  • Understanding of clinical trial process and clinical systems are added advantage

  • Awareness of CDISC standards (CDASH, SDTM, ADaM) is added advantage

  • Awareness of Clinical Dictionaries – MedDRA and WHODD is added advantage

  • Understanding of regulations including ICH-GCP and 21 CRF part 11 is added advantage

  • Programming skills required if deputed in sub-function – Data Standards and SDTM & Programming (e.g., SAS, SQL, Cognos), sub-function – Validation (e.g., automation tools like Selenium, HP ALM), sub-function – Data Acquisition (e.g., PL/SQL, SAS, Python, C++)

How to apply :

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