Researcher, Trials (Norstella)

Roles and Responsibilities

Responsibilities

• Identify and extract key drug data from public sources (e.g., clinical trial registries, regulatory filings, company report)

• Demonstrate working knowledge of FDA, EMA, and other global regulatory agencies’ processes.

• Apply foundational knowledge of therapeutic areas and mechanisms of action (MoAs) to drug research

• Adhere to SOPs and gather information from source publishing processes

• Check and validate content for accuracy and basic errors before submission

• Meet daily and weekly productivity targets while ensuring data quality

• Develop proficiency in authoring tools and extensions to support publishing.
  

Qualifications

• Graduate/Post-Graduate/Doctorate degree in Life Sciences, Pharmacy, Medical Sciences, or a related discipline

• Minimum 1 year of experience in pharmaceutical research, clinical data, or drug content development preferred

• Understanding of regulatory databases (e.g., ClinicalTrials.gov, EMA, FDA) and public data sources

• Familiarity with drug development lifecycle, therapeutic areas, and MoAs

• Proficient in MS Office Suite, especially Excel and Word.
  

Benefits

• Health Insurance

• Provident Fund

• Life Insurance

• Reimbursement of Certification Expenses

• Gratuity

• 24x7 Health Desk