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2 weeks ago
A skilled Medical Writer is needed to create high-quality medical content.
Key Responsibilities:
- Create accurate and informative medical documents, including clinical trial reports, regulatory submissions, and educational materials.
- Develop and implement effective content strategies to engage target audiences and meet business objectives.
- Collaborate with cross-functional teams, including scientific experts, designers, and project managers, to ensure seamless execution of projects.
Required Qualifications:
- Education: Bachelor's or Master's degree in Life Sciences, Pharmacy, or a related field.
- Experience: 5-10 years of experience in medical writing/scientific communications within the pharmaceutical industry.
- Skills: Publication and regulatory writing skills, literature database proficiency (PubMed, EMBASE, Cochrane, etc.) and reference management skills (EndNote, Mendeley, Zotero).
- Knowledge: Familiarity with EMA, FDA, HTA, NICE, and WHO guidelines.
- Understanding: Understanding of systematic reviews, RWE/HEOR, and statistical interpretation.
Benefits:
The ideal candidate will have a passion for science communication and be looking for a challenging opportunity to showcase their skills and expertise.
Other Requirements:
Proficiency in Adobe Suite, Veeva PromoMats, and statistical software (SPSS, R, SAS, Prism) is highly desirable. Therapeutic area expertise, such as Oncology, Immunology, Neurology, Rare Diseases, is also an asset.
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