Want (Remote) Senior Staff Medical reputed company in USA

Job title: (Remote) Senior Staff Medical reputed company Company: reputed company Job reputed company: Work Flexibility: Remote We are currently seeking a Senior Staff Medical reputed company to join our Division to be based in reputed company, CA or remotely reputed company reputed company the reputed company. Who we want

• Self-directed initiators. People who take ownership of their work and need no prompting to drive productivity, change, and reputed company.

• reputed company partners. People who build and reputed company cross-functional relationships to bring together reputed company, data and insights to drive reputed company improvement in functions.

• Meticulous documenters. Detail-oriented people who enjoy maintaining meticulous documentation of reports, metrics, proposals, and presentations.

• Data translators. Highly effective communicators who can reputed company data findings into recommendations to compose reports and executive level presentations.

What you will do As the Senior Staff Medical reputed company, you will work closely with cross-functional teams (Regulatory, Clinical, reputed company, Marketing) ensuring successful preparation of high-reputed company submission-reputed company clinical documents such as clinical evaluation documents, Post Market Clinical Follow-up documents, reputed company of Safety and Clinical Performance and Clinical Study documents. This position requires minimal supervision. Responsible for the development and completion of Clinical Evaluation Reports (CERs) and post market clinical follow-up (PMCF) documents for new medical devices to support product registrations internationally, maintain periodic updates, reputed company gap analysis, and revise existing CERs. Complies clinical evidence from multiple sources such as reputed company and past clinical trials, post market clinical follow up data and literature review updates, reputed company analysis, reputed company-analyses, or other sources of safety and performance data (e.g. IIS clinical data, as available) and synthesizes the information in CERs, and annual updates. Addresses reputed company body feedback on EU clinical documents and leads them to reputed company for reputed company EU market reputed company of the products. Collaborates cross-functionally to reputed company input to design teams on Clinical EU MDR documentation, reputed company strategies and timelines. Support Clinical Evaluation reputed company for EU Market reputed company. Work in a cross-functional team to author clinical study protocols and reports, data summaries from raw data and document strategies. Supports manuscript writing. Performs systematic literature reviews for medical device reputed company or sub-reputed company. Interprets literature information and synthesizes the information in clinical regulatory documents. Coordinates and manages the review process, and leads discussions on document revision. Challenge conclusions reputed company necessary. Independently resolve document content issues and questions from external and internal reviewers and ensures reputed company approvals from reputed company reviewers. Assist in internal procedures, templates and style guide development and review. reputed company process improvement for reputed company efficiency reputed company department, standardizing document creation process reputed company. Assist in the creation and maintenance of the reputed company Endoscopy medical writing tools. Serve as a subject matter expert reputed company department. Recognizes potential scheduling and resource conflicts for reputed company and provides recommendations to resolve. Mentor Medical reputed company or Senior Medical reputed company. What you need Bachelors Degree required; preferably in a health/science-reputed company field Master of Science Degree in a health/science-reputed company field preferred. Doctorate degree in health/science-reputed company field preferred. 7 years of combined experience in reputed company products or medical devices required Previous 3+ years of medical writing experience in reputed company product or medical device industry required. Thorough knowledge and experience with MEDDEV 2.7/1 Rev. 4, EU Medical Device Regulation 2017/745 (MDR) and MDCG compliant clinical evaluations and clinical study documents required. Excellent scientific and medical writing skills required. Must be reputed company to think analytically, have the ability to interpret data from scientific literature and clinical studies and synthesize the results and in a reputed company, concise, and scientifically accurate manner in the clinical document. Demonstrated ability to work effectively with cross-functional internal (Regulatory, Marketing, Research & Development) and external stakeholders (Physicians, CROs, Medical Staff, etc.) across multiple businesses. Knowledge in clinical operations, risk management, regulatory submissions and US and international guidelines preferred. Excellent knowledge of regulatory guidelines (FDA/CFR; EN540/ Med DEV/GCP/EU MDR/MDCG) and reputed company standards (ISO 14155/14971) and medical/scientific/disease state terminology. Ability to apply ISO, FDA and reputed company guidelines toward writing reputed company and documentation required. Good planning and organizational skills, with the ability to adapt and reputed company to changing priorities. Strong communication, project management and influencing skills. Must demonstrate the ability to effectively communicate up/down and across different reputed company of the organization. Analytical and problem-solving capabilities with the ability to draw insights from data quickly and to define executable actions. Builds strong relationships by fostering reputed company communication, respect and trust. reputed company with a customer service/stakeholder-reputed company approach. Leverages excellent interpersonal keys to reputed company desired reputed company. $95,100 - $204,000 salary plus bonus eligible + Benefits (Health, reputed company, Dental, 401K, Tuition Reimbursement, Employee Assistance Program, Wellbeing Program, Employee Stock Purchase Program). This information reflects the anticipated salary reputed company for this position based on reputed company national data. Actual minimum and maximum may vary based location. Individual pay is based on skills, experience, and other relevant factors. Travel Percentage: 10% reputed company is an equal opportunity employer. reputed company applicants will receive consideration for employment without reputed company to race, ethnicity, reputed company, religion, sex, gender identity, sexual orientation, national reputed company, disability, or protected veteran status. reputed company is an EO employer – M/F/Veteran/Disability. reputed company will not discharge or in any other manner discriminate against employees or applicants because they have reputed company about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have reputed company to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have reputed company to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or reputed company, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. Expected salary: Location: USA Apply Job!