Fircroft Qatar Careers 2023-Apply for Principal Medical Writer – CRO Jobs Vacancy

  • Full Time
  • Qatar

Website Fircroft Qatar

Principal Medical Writer – CRO

Fircroft Qatar Job Vacancy at Principal Medical Writer – CRO in Qatar

Principal Medical Writer – CRO Jobs 2023 in Qatar :- Principal Medical Writer – CRO has publish a notification on career page for the recruitment of Fircroft Qatar Post in Qatar location. Candidates who are eligible for the post of Fircroft Qatar can apply on before last date without getting late.

Comapny Name Fircroft Qatar 
Name of Post Principal Medical Writer – CRO
Salary QAR 26,486.00 per month
Job Location Qatar
Job type Qatar Jobs

Principal Medical Writer – CRO Jobs in Qatar 2023 Full Job Descripation

Principal Medical Writer

NES Fircroft is seeking an experienced Medical Writer who will confidently lead medical writing projects across this dynamic and growing boutique CRO!

You’ll provide project leadership across all development, writing & editing of scientific, clinical content, Investigator Brochures (IB), Clinical Trial Protocols, Participant Information Consent (PIC) and Clinical Study Reports, as well as ensuring medical accuracy & regulatory compliance across promotional tools. Developing SOPs, internal guidelines & best practice for content development.

An exciting opportunity to join a CRO with plenty of further career growth opportunities within as they continue to expand!


  • act as a scientific consultant and medical writer; provide scientific and regulatory support to clients and internal teams
  • provide scientific strategy on study designs; plan and develop Early Phase study designs/synopses/protocols, IBs
  • clinical data analysis, CSRs development based on international standard and sponsor’s unique requirements
  • quality control activities (regulatory documents, SOPs, SAP, AMIS, TFLs)
  • ensuring that study designs are adequate and meet study objectives while ensuring subjects’ safety
  • participation in reviewing Early Phase protocols prepared by clients
  • accountable for scientific leadership and deliverable on assigned activities throughout the project conduct
  • submission of regulatory materials (FDA, Health Canada, HREC)
  • keep track of assigned documents/deliverables until the end of the study and deliver within required timelines; address and manage related issues.
  • independently prepare and present scientific material at internal and client calls
  • lead projects autonomously from beginning to the end

To be successful, you will have;

  • A positive ‘can do’ attitude
  • Suitably qualified with Medical, Life Science or equivalent degree(s)
  • Experience writing regulatory documentation including study reports & protocols
  • Thorough medical terminology knowledge & good understanding of clinical trial processes and ICH GCP guidelines
  • Excellent verbal & written communicator
  • Ideally experience in developing & delivering training programs within Medical Writing
  • Good understanding of drug development & awareness of regulatory affairs
  • Australian Citizen or Permanent resident

Apply Now

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