![]() ![]() Minimum of a BA/BS in Life Science graduate degree preferred.Ability to function in an ambiguous environment.Excellent computer skills including MS Office (Word, Excel, Power Point, Outlook) experience with electronic document management systems and other content authoring technologies preferred.Applies good judgment and demonstrates initiative to resolve issues.Ability to identify process improvements, manage change successfully, work with newer technologies, and foster an innovative atmosphere. Minimum of 2-3+ years of experience in medical education preferred, or relevant experience in pharmaceutical advertising, medical publishing, or medical.Ability to collaborate with a wide variety of internal customers and relate effectively to people at all levels of the organization.Good leadership, communication, and influencing skills.Experience with ICH and electronic submission guidelines for regulatory report+C58s+C58 written and verbal skills.Provide high-quality medical & scientific. Medical writing experience in Pharma, Biotech and/or CRO medical device experience preferred. 30+ days ago 100 Remote Job Full-Time Employee Canada, or US National As a Senior Medical Writer, you will serve as the primary author by writing and providing input on routine documents such as clinical study reports and study protocols and summarizes data from clinical studies.Ability to interpret and organize scientific and clinical data. ![]() Demonstrated expertise in writing/developing clinical documents in support of global regulatory submissions.Must have exp working with clinical or regulatory documents. Supports innovation initiatives within the Medical Writing Group.Ensures medical writing activities meet quality standards and expectations and adhere to applicable Corporate SOPs, WPs, policies, guidelines and regulations.Engages with team members to ensure medical writing continues to deliver value to the business.Assures that standardized practices are implemented and maintained across all therapeutic areas.Adheres to medical writing practices/systems/tools to support clinical studies in order to meet company goals and objectives.Authors deliverables with consideration for regulatory, corporate, departmental, and quality standards (documents include but are not limited to protocols, clinical study reports, Investigator’s Brochures, annual reports, HA briefing packages and response documents, submission summary modules, and integrated data summary reports).Contributes to therapeutic project teams as the medical writing expert for clinical and regulatory submission documents.New York to its west, and Long Island Sound to its south. Proactively manages writing activities across assigned projects as appropriate, ensuring adherence to the medical writing strategy and alignment with business needs. The average medical writer salary in Connecticut, United States is 99330 or an equivalent. ![]()
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