Selected: 🏥📝 Medical Writer.
Selected: 🇮🇳 India – Remote.
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Selected: 🆕 Date Added.
🕒 5 days ago
Medical Writer producing clinical study reports, protocols, and regulatory documents for Thermo Fisher Scientific. Supporting pharmaceutical research projects through scientific writing and data interpretation.
🕒 October 29
Senior Medical Writer and Evidence Analyst supporting Worldwide Clinical Trials, a global CRO. Contributing to high-quality clinical research and life-changing therapies.
🕒 October 22
Medical writer developing global regulatory submissions for Syneos Health’s biopharmaceutical clients. Managing cross-functional timelines, quality documents, process improvements, and junior writer mentorship.
🕒 October 15
Principal medical writer producing clinical and scientific documents for pharmaceutical and clinical research clients. Leading reviews, mentoring writers, and supporting regulatory and program management activities.
🕒 October 15
Medical Writer authoring clinical and regulatory documents for Quanticate, a global data-focused CRO. Leading projects, supporting clients, and mentoring writers across clinical development programmes.
🕒 October 7
Senior Medical Writer creating clinical and regulatory documents for Syneos Health’s life sciences research services. Coordinating reviews, regulatory compliance, and cross-functional study deliverables.
🕒 October 6
Senior Medical Writer leading clinical trial disclosure submissions at Parexel, a global clinical research organization. Guiding regulatory compliance, client decisions, and junior writer development.
🕒 September 15
Freelance Clinical Medical Writer creating clinical trial documentation for TransPerfect. Producing protocols, study reports, informed consent forms, and investigator brochures.
🕒 September 15
Freelance Clinical Medical Writer creating clinical-trial protocols, reports, consent forms, and investigator brochures for TransPerfect’s localization services.
🕒 April 9
Senior Medical Writer authoring and reviewing regulatory medical writing deliverables for clinical studies. Supporting other writers and undertaking quality control across various domains while adhering to ICH regulations.
🕒 April 9
Principal Medical Writer crafting regulatory and medical writing deliverables for Catalyst Clinical Research. Collaborating on projects and supporting other writers while ensuring quality standards in medical documentation.
🕒 March 5
Medical Writer I role at Syneos Health focusing on clinical study documentation and regulatory project support. Collaborating with teams to ensure quality medical writing deliverables.
🕒 January 8
Senior Medical Writer managing medical writing activities for Syneos Health. Leading document development and regulatory compliance with a focus on clinical and commercial insights.
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