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Merck & Co, Inc (7)
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Easy Apply only
Leads the development and authoring of abstracts and slides or posters presenting clinical study data at medical congresses and the development of primary manuscripts for publication in peer-reviewed...
Familiarity with the drug development process (discovery to market), clinical study protocol design and study conduct, documentation required for the conduct of clinical studies, and clinical study da...
Collaborate with internal and external stakeholders to develop manuscripts and congress materials (abstracts, posters, oral presentations) in accordance with timelines set in the publication plan...
Draft high-quality clinical & regulatory documents that demonstrate a good grasp of the scientific and medical content and drug development process with excellent understanding of data analysis, data...
Develop a detailed knowledge of assigned therapeutic area(s), client and competitor product(s), the compliance/regulatory environment, and international standards for disclosing medical/scientific con...
Knowledge and skills as a medical writer, literature evaluation, and multi-level response development. Excellent interpersonal, oral and written communication and presentation skills required...
Accountable for the scientific aspects of the implementation and conduct of a clinical trial (e.g., investigator meeting presentations, safety and medical monitoring)...
Ensure that documentation conforms to International Conference on Harmonization (ICH) and other relevant regulatory guidelines and medical editorial boards; ensure that appropriate documented quality...
Provides leadership in biometrics activities pertaining to study projects. Collaborates with project teams on design and analysis of clinical trils; selects appropriate statistical methods for design...