GlaxoSmithKline (GSK) is a leading global biopharma company dedicated to uniting science, technology, and talent to combat diseases. Our mission is to positively impact the health of billions, fostering a culture where employees can thrive, grow, and make meaningful contributions. With a focus on innovative medicines, vaccines, and specialty treatments, GSK operates in core therapeutic areas such as infectious diseases, respiratory/immunology, oncology, and HIV. We believe that our success is rooted in the diverse talents of our workforce, and we strive to create an inclusive environment where everyone feels valued and empowered.
Responsibilities in the Job
As a Literature Specialist Intern at GSK, you will play a pivotal role in supporting the Central Safety Department (CSD) with literature screening activities related to Individual Case Safety Reports (ICSR) and signal detection. Key responsibilities include:
- Conducting thorough literature surveillance activities in compliance with pharmacovigilance regulations.
- Supporting SERM product specialists by identifying important safety information from a wide range of publications relevant to GSK’s diverse product portfolio.
- Screening and reviewing literature search results (including articles, abstracts, and citations) to identify relevant safety information.
- Triaging literature search results to determine articles of interest for GSK marketed products and those in development, using established algorithms and criteria.
- Ensuring the timely production of key deliverables and maintaining accurate records.
Qualifications
To be considered for the Literature Specialist Intern position, candidates should meet the following qualifications:
- Education: A Bachelor’s Degree in Life Sciences (e.g., Biology, Chemistry, Pharmacy, Medicine) is required. Preference may be given to candidates with degrees in Pharmacy, Medicine, or Pharmacology.
- Experience: 0 to 2 years of relevant industry experience, preferably in the pharmaceutical sector, with a focus on drug safety and regulatory compliance.
Skills
To succeed in this role, candidates should demonstrate the following skills:
- Language Proficiency: Strong command of the English language, both written and verbal, particularly in scientific and medical terminology.
- Analytical Skills: Ability to evaluate data, draw conclusions, and make informed decisions, with guidance from senior team members.
- Attention to Detail: High level of detail orientation is crucial in assessing literature and ensuring accuracy in deliverables.
- Communication Skills: Excellent interpersonal and presentation skills, with an ability to translate complex scientific information into understandable messages for diverse audiences.
- Technical Proficiency: Familiarity with computer applications and web-based platforms to perform literature searches and data analysis.
- Flexibility and Prioritization: Ability to manage multiple tasks effectively and adapt to changing priorities in a fast-paced environment.
