Lead medical writing projects for Clinical Research Scientists, Academic partners, Sponsors and/or the Corporation. Interpret and translate complex technical research data, findings or methodologies into academic/scientific publications, regulatory documents (protocols, investigator brochures, clinical study reports, etc.) and/or presentations on a timely basis that align with industry, regulatory and academic style and content guidelines and standards. Embrace a continuous learning mindset and be able to manage writing projects of increasing complexity, including those stemming from studies with novel or innovative research designs. Coordinate document reviews with authors. Develop and track timelines for assigned writing projects. Provide mentorship and support to other writing team members. Act as primary contact for external publishing if required. Assist with review or editing of other materials (training, communications, sales, grants, study operations, etc.) when requested.
Boston, Raleigh, Atlanta, TampaRead More