Job highlights
Knowledge of ICH guidelines,Good Clinical Practices (GCP) and
Valuable Knowledge of Medical terminology and clinical concepts. Additional notes: .
Preparation of protocol for Clinical trials ICF (Informed Consent Form, CRF (Case Report Form) writing and quality review
Preparation writing CSR (Clinical Study Report) as per ICH guidelines
Literature survey, feasibility check.
To submit documents related to IEC/DCGI for approval
Knowledge of ICH guidelines, Positive Clinical Practices (GCP) and Applicable regulation and guidelines related to the Clinical trials.
Performs quality control(QC)review of clinical study report and relevant documents.
Valuable Knowledge of Medical terminology and clinical concepts.

Additional notes
Candidates with flair in English and medical writing for clinical trials
You can also explore candidates who are having QC profile in medical writing
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📌 Medical Writer Clinical Trial Mumbai (India)
🏢 Acme Services
📍 India