![]() If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation in using our website for a search or application, please contact us. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance. Stratacuity will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. Medical Writing Operations QC Manager (Remote) Vertex Pharmaceuticals 3.7. ![]() All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law. Stratacuity is an Equal Employment Opportunity/Affirmative Action Employer. We will not share your information with anyone without your direct prior consent. Upon receiving your inquiry, you may be directly contacted by a Stratacuity team member to discuss your career goals. We build lasting relationships with exceptional biopharmaceutical talent and take great care to protect your personal information. Whether you are seeking a career change or simply interested in becoming part of our network, you will appreciate the ethics guiding each Stratacuity team member. Work cross functionally with internal and external stakeholdersīS degree in a scientific, medical, or clinical discipline (Advanced degree preferred)ģ - 5 years of clinical / regulatory writing experienceĮxperience with authoring and reviewing submission documentsĮxperience with End Note and Starting Point Represents Medical Writing on project teams to serve as SME for clinical development documents. Manages efficient review and finalization of documents Maintains timelines and workflow of writing assignments Director and requires coming onsite (Newton, MA) 2 days a week.Īuthor clinical development documents (clinical protocols, IBs, CSRs, ICFs and more) This person will join an existing team, reports into the Sr. ![]() This position will work across a number of preclinical and clinical programs and be responsible for providing medical writing expertise, including data review and analysis activities.
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