Looking for a great career at a cutting edge service provider to pharmaceutical companies and regulatory authorities? Soterius is looking for talented go-getters who are committed to our values of excellence and uncompromising quality.

We’re looking to fill a variety of roles, so check out the openings below to see if there’s the right fit for you. Contact us to receive detailed job descriptions and requirements.

Medical Information Specialist

Job Location: New Delhi, India

We are looking for energetic and enthusiastic Healthcare Professionals (HCPs) to work for a customer focused organization. Candidates should have a minimum of 3 years of experience working in medical information operations for CROs or pharmaceutical companies. You are expected to:

  • Handle medical enquiry calls using a list of frequently answered questions (FAQs)
  • Draft responses for special medical information requests
  • Develop and maintain Standard Response Letters (SRLs) in conjunction with our clients
  • Have fluency in reading, writing and speaking English
  • Work late/night shifts, if required* 

Qualifications: B.Pharm/M.Pharm/BDS/MBBS/MD or equivalent qualification from a reputed university.

*Home based/remote working can be considered for suitable candidates.

Medical Reviewers

Job Location: New Delhi, India

We are looking for energetic and passionate professional to work as  a Medical Reviewer for a fast-paced customer-focused service provider.

You should be:

  • MBBS/MD with minimum 2 years of experience as a medical reviewer
  • Available to join immediately (preferred)
  • Passionate about patient safety
  • Based out of or willing to move to New Delhi

Job Responsibilities:

  • Conducting review and assessment of ICSRs obtained from various sources (clinical trials/post-authorization)
  • Determining reportability of cases obtained from various sources
  • Triaging cases and determining seriousness and relatedness for the assigned products
  • Reviewing appropriate selection of adverse events from source documents, assigning appropriate MedDRA code and reviewing case narratives.
  • Acquiring complete knowledge of the product portfolio and safety profiles for products across therapeutic areas.
  • Involved in clinical safety, signal and risk management and review of aggregate reports
  • Performing any other pharmacovigilance related activities as assigned.
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