Duties and Responsibilities:
Reviews and interprets data (tables, listings, graphs) and source documents (provided or accessed directly from a clinical database) to draft, solicit comments, edit, and finalize an IDE (investigational device exemption) study annual report for FDA.Works with individuals in other functional areas to identify and resolve clinical and statistical issues in the interpretation of clinical data. Conducts literature searches, as appropriate, to provide useful references supporting findings/conclusions in the study report May also have other writing, proof-reading, or editorial duties related to other clinical deliverables (e.g., clinical overviews, abstracts, manuscripts, etc.)
Essential Job Functions:
Authors clinical documentation- mainly the Clinical Evaluation Reports (CER), including the clinical section of regulatory authority requests for the entire portfolio. Acquires knowledge of therapeutic areas, competitor devices, current clinical/market developments, literature review processes and the ability to stay current with current literature. Develops comprehensive, systematic literature search protocols, supports in-depth literature searches for CERs and other clinical evidence reports and gains knowledge and understanding of current scientific literature required to support identified product lines and related clinical studies. Responsible for staying informed about applicable clinical landscapes and trends. Provides product guidance to Clinical Affairs, Scientific Affairs, Medical Affairs and other functions (as appropriate) to help with conducting literature searches on products/product families. Reviews literature, interprets and summarizes risks, analyzes alternative therapies and device specific benefits from literature; collects and summarizes primary data to support risk assessment. Critically appraises scientific literature and writes clinical summaries for products and procedures. Responsible for proofreading, editing, formatting, and reviewing comment integration and document completion/approval activities. Performs periodic reviews of risk documentation and product labeling; ensures appropriate updates are implemented. Provides clinical perspective and support to guide new product development for CE Mark/International product registration purposes. Authors protocols and/or routine clinical study progress reports. Ensures compliance with corporate (e.g., SOPs) and regulatory requirements (e.g., GCP and US and OUS guidelines).May support other medical writing/scientific communication efforts (I.e. peer reviewed publication, white paper, podium presentation) as requested Other duties as requiredEOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. To find out more about Real, please visit
