Required Experience & Qualifications
2-4 years of experience in medical writing, preferably in clinical trials, regulatory, or patient-facing content.
Hands-on experience working with Informed Consent Forms (ICFs) or patient education materials is strongly preferred.
Bachelors degree in life sciences, pharmacy, medicine,nursing, biomedical sciences, or a related field.
Key Skills & Competencies
Excellent written and verbal communication skills with a strong command of English.
Proven ability to simplify complex medical and scientific information for lay audiences.
Strong attention to detail with the ability to preserve
meaning, balance, and neutrality in patient communications.
Comfort working with narrative or screenplay-style formats for audio-visual content.
Ability to work collaboratively with cross-functional teams in a structured, deadline-driven environment.
Preferred / Nice-to-Have Skills
Experience with eConsent, patient engagement tools, or multimedia content development.
Familiarity with global clinical trial environments and multi- country consent requirements.
Exposure to health literacy principles or patient-centric communication approaches.
Disclaimer : This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
Keyskills: audio visual Nursing Pharmacy Clinical trials Life sciences biomedical Medical writing Content development
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