Lead scientific writing projects for Clinical Research Scientists, Sponsors, Academic partners, and/or Alimentiv. Interpret and translate complex technical research data, findings or methodologies into regulatory documents (protocols, investigator brochures, clinical study reports, informed consent forms, etc.) on a timely basis that align with industry, regulatory and academic style and content guidelines and standards. Coordinate document reviews. 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 (grants, study operations, training, communications, etc.) when requested.
Amsterdam, Toronto, London (UK), Frankfurt, Raleigh, Vancouver, Montreal, ChicagoRead More