We are growing, grow with us!
Are you looking for a dynamic company with daily new challenges and opportunities?
Then, Pharmalex is your career opportunity. Pharmalex is one of the leading service companies for the Pharmaceutical Industry globally and is specialized in all aspects of drugs and medical devices approval, of the market development and any action of effective product maintenance.


Senior Specialist , Medical Writing

Your Job

  • To author, review and independently manage high quality clinical documents: Clinical Study Reports (CSR) including narratives, Protocol, Informed Consent Form (ICF).
  • Contribute to planning of data analyses and presentation to be used in CSRs; Ensure compliance of documentation
  • Excellent data interpretation skills.
  • Understanding of ICH-E6 and E3 guideline.
  • Understanding of template for Protocol as per ICH-E6 and Transcelerate Common trial protocol
  • Basic understanding of statistics


Minimum 2 years in CSR/Protocol



If you are interested in joining our Pharmalex team taking over this challenging job opportunity in our future-oriented company, we are looking forward to receive your application documents stating your earliest possible starting date, any visa requirements and salary expectations on-line.

For further information please don’t hesitate to contact us:

Ms. Vineeta Bisht
Manager, Human Resources India