- Integra LifeSciences (Trenton, NJ)
- …+ Medical device experience is preferred (510(k), PMA, BLA, HCTP). + Experience in regulatory writing is preferred. + Skilled in written and oral communications. ... outcomes and set new standards of care. The **Associate Manager , Medical Writing ** is a senior level...clinical deliverables in accordance with internal GSOPs, and regulatory guidelines including clinical sections for … more
- BeOne Medicines (San Mateo, CA)
- …global clinical operations, start-up, regulatory , safety, medical & clinical sciences, data management, biostatistics, medical writing , and other units. ... Senior Manager Clinical Costing System and Pricing will support the development, enhancement, and governance of our enterprise resource need estimating tool for… more
- Centers for Independence (Milwaukee, WI)
- …Travel Percentage **None** Category **Health Care** **Description** **Job Purpose:** The clinical manager is responsible for organizing and directing the ... directs and evaluates the performance of all staff who report to the clinical manager including formal reviews and performance recognition, feedback and… more
- Stanford Health Care (Palo Alto, CA)
- …of assigned areas of responsibility for the Anatomic Pathology and Clinical Laboratories. Ensures that programs, policies, and procedures are established and ... implemented to meet customer needs, department standards, and regulatory agency requirements. Assesses and determines the staffing needs and practices of the… more
- BeOne Medicines (Emeryville, CA)
- …and execution of the Clinical Study Report in collaboration with Global Clinical Study Manager and Medical Writing **Quality:** + Handles escalated ... progress in the region to senior management and Global Clinical Study Manager as required + Represents...other key stake holders to ensure timely submission to regulatory authorities and ECs/IRBs + Accountable for submissions of… more
- BeOne Medicines (San Mateo, CA)
- … operations teams and medicator monitor) + Ensures planning and execution of the Clinical Study Report in collaboration with Medical Writing and relevant CST ... within agreed timelines and budget + Leads all aspects of assigned clinical study(ies) + Leads global cross-functional study team (including oversight of external… more
- BeOne Medicines (Emeryville, CA)
- …is responsible for the development of patient safety narratives for Phase 1-4 clinical trials in accordance with the client's controlled processes based on data ... and/or safety reports (eg, CIOMS). **Essential Functions of the job:** **Narrative Writing ** **:** + Writes, edits, reviews, finalizes, and tracks patient safety… more
- BeOne Medicines (San Mateo, CA)
- …and execution of the Clinical Study Report in collaboration with Global Clinical Study Manager and Medical Writing **Quality:** + Handles escalated ... progress in the region to senior management and Global Clinical Study Manager as required + Represents...other key stake holders to ensure timely submission to regulatory authorities and ECs/IRBs + Accountable for submissions of… more
- Olympus Corporation of the Americas (Westborough, MA)
- …commercialization of Olympus's portfolio. Specifically, this individual will be responsible for writing clinical study protocols, case report forms, and study ... between Sales and Marketing, R&D, PMO, HEMA, Risk Management, Quality and Regulatory Affairs, and investigational sites. + Ensures clinical studies are… more
- Endo International (Greenville, IL)
- …operation of the Greenville Quality Department to ensure product quality and regulatory compliance. The Quality Manager will champion the continued ... expert. + Strong patient and customer focus. **_Skills/Competencies:_** + Strong writing skills to effectively communicate technical/ clinical information to… more
- Stanford Health Care (Newark, CA)
- …Day - 08 Hour (United States of America) The Advanced Practice Provider (APP) Manager for Clinical Advice Services (CAS) will be supporting a team comprised ... Medicine. As a manager at CAS, you'll set the standard for clinical teletriage, shape process improvement, and contribute to a culture of continuous learning and… more
- DESC (Seattle, WA)
- Project Manager - Day Shift, MRRCT Seattle, WA (http://maps.google.com/maps?q=1618+S+Lane+Street+Seattle+WA+USA+98144) -MRRCT Apply Job Type Full-time Description ... instabilities in our community. **JOB DESCRIPTION:** The MRRCT Day Shift Project Manager is responsible for overseeing a highly motivated and effective crisis… more
- Stanford Health Care (Redwood City, CA)
- …sector? Join Stanford Health Care's dynamic Cancer Center project as a Project Manager and help deliver innovative spaces that redefine cancer care. You'll oversee ... projects. + Act as liaison between clients, consultants, contractors, and regulatory agencies, ensuring clear communication and project alignment. + Implement… more
- Moses/Weitzman Health System (Meriden, CT)
- …Description Summary:** **Job Description:** JOB SUMMARY The School Health Regional Manager is responsible for the overall business operations in assigned region(s). ... The School Health Regional Manager will be responsible for leading and managing daily...sets performance objectives, evaluates and optimizes operational performance, ensures regulatory and company standards are upheld, and prepares operation… more
- Parexel (Washington, DC)
- …guidelines and regulations. + Broad experience in preparation of all types of clinical regulatory documentation. Experience in management of complex medical ... analyze, and evaluate pertinent resources to prepare, develop, and finalize key clinical documents for submission to regulatory authorities, without the need… more
- Parexel (Phoenix, AZ)
- …analysis plans and mock statistical output to determine appropriateness of content/format for clinical writing . **Quality Control** + Ensure that all work is ... deliverable timelines, project leadership, and training and support of junior medical writing staff. **Key Accountabilities** : **Author Clinical Documents** +… more
- Parexel (Baton Rouge, LA)
- …leverage your medical expertise to ensure the safety of patients in clinical trials and post-marketing settings. In this pivotal role, you'll perform comprehensive ... while tackling complex safety evaluations that directly impact patient wellbeing and regulatory compliance. **About the Role** As a **Senior Physician in Patient… more
- Terumo Medical Corporation (Elkton, MD)
- …products, training and education programs that drive clear economic value, better clinical outcomes and improved quality of life for patients. TMC is part ... and, when possible, cost reductions, through the review & writing of new or revised procedures; Assisting with third... of new or revised procedures; Assisting with third party/ regulatory audits and administration of the Adverse Event Reporting… more
- GRAIL (Menlo Park, CA)
- …and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome ... total work week be on-site. Your specific schedule, determined in collaboration with your manager , will align with team and business needs and could exceed the 40%… more
- Stanford Health Care (Palo Alto, CA)
- …therapist who performs routine patient care and is responsible for all clinical aspects of assigned patient care, including evaluation and treatment, with ... supervision as needed. The Occupational therapist I is proficient in providing basic clinical care, however is expected to seek guidance from and collaborate with… more
