Expertly delivering clinical trials operations, with care.
Freelance Senior Medical Writer experienced in medical devices
Location
Europe + 1 moreAll locations: Europe | Eastern Europe
Posted
10 days ago
Salary
0
Seniority
Senior
No structured requirement data.
Job Description
Freelance Senior Medical Writer experienced in medical devices
Excelya
Role Description We are seeking a Freelancer Senior Medical Writer, experienced with medical devices for a part-time role, to provide medical and scientific expertise required for the successful completion of Excelya’s projects. The position is fully remote and the candidates can be based in every EU country or Armenia. - Preparation of PMCF, CER, CEP, PMS. - Review of relevant documents. - Consultation and gap analysis on transition from MDD to MDR. - Responses to queries from regulatory authorities. - Perform literature search. - Appraise literature search data. - Ability to interpret, evaluate, and translate medical research findings. Qualifications - Degree in Life Sciences. - At least 4-5 years of experience in medical writing. - Experience in medical device-related documents (CEP/CER/PMCF/PSP). - Fluent in English. - Knowledge of French language is a plus. - Submissions to FDA is a plus (for medical devices). - Regulatory consultation is a plus. Benefits - High-impact projects that nurture your potential. - Space to shine and push boundaries. - Becoming a key part of something bigger.
Related Guides
Related Categories
Related Job Pages
More Medical writer Jobs
Role Description We are seeking a Freelancer Senior Medical Writer, experienced with medical devices for a part-time role, to provide medical and scientific expertise required for the successful completion of Excelya’s projects. The position is fully remote and the candidates can be based in every EU country or Armenia. - Preparation of PMCF, CER, CEP, PMS. - Review of relevant documents. - Consultation and gap analysis on transition from MDD to MDR. - Responses to queries from regulatory authorities. - Perform literature search. - Appraise literature search data. - Ability to interpret, evaluate, and translate medical research findings. Qualifications - Degree in Life Sciences. - At least 4-5 years of experience in medical writing. - Experience in medical device-related documents (CEP/CER/PMCF/PSP). - Fluent in English. - Knowledge of French language is a plus. - Submissions to FDA is a plus (for medical devices). - Regulatory consultation is a plus. Benefits At Excelya, we lead with Audacity, act with Care, and move with Energy. We nurture your potential through high-impact projects, give your talents the space to shine, and push boundaries to elevate every patient’s journey. Here, you're not just doing a job—you’re becoming a key part of something bigger.
Registered Nurse - Clinical Documentation Specialist
University of VirginiaThe University of Virginia is an equal opportunity employer. All interested persons are encouraged to apply, including veterans and individuals with disabilities. Learn more about UVA’s commitment to non-discrimination and equal opportunity employment.
Role Description The Clinical Documentation Specialist is responsible for the evaluation of physician documentation utilizing their clinical expertise to ensure the patients’ severity of illness is accurately portrayed in the medical record for specificity of coding and increased coding accuracy. They provide guidance to the physicians, nursing, and ancillary staff on clinical documentation best practices. They must be self-motivated and adaptive to change. - Responsible for the day-to-day evaluation of inpatient documentation in accordance with the Clinical Documentation Program requirements. - Ensures the accuracy and completeness of clinical information used for measuring and reporting physician and hospital outcomes. - Communicate with members of the medical staff on an ongoing basis to assure the documentation in the medical record adequately reflects the diagnoses being treated and the procedure performed. - Other duties may be assigned in addition to the above job responsibilities. Qualifications - RN, graduate of accredited nursing program and Bachelor of Science in Nursing required within 5 years of hire. - A minimum of three years of experience as a Clinical Documentation Specialist is required. - Clinical experience in multiple areas, particularly in the ICU, is preferred. - Licensed to Practice as a Registered Nurse in the Commonwealth of Virginia. Requirements - Reference Checks will be completed by UVA’s third-party partner, SkillSurvey, during the final phase of the interview process. - Five references will be requested, with at least three responses required. Benefits - Comprehensive Benefits Package: Medical, Dental, and Vision Insurance - Paid Time Off, Long-term and Short-term Disability, Retirement Savings - Health Saving Plans, and Flexible Spending Accounts - Certification and education support - Generous Paid Time Off Company Description UVA Health is a world-class Magnet Recognized academic medical center and health system with a level 1 trauma center. The 2023-2024 U.S. News & World Report “Best Hospitals” guide rates UVA Health University Medical Center as “High Performing” in 5 adult specialties and 14 conditions/procedures. - One of 70 National Cancer Institute designated cancer centers. - UVA Health Children’s is named by 2023-2024 U.S. News & World Report as the best children's hospital in Virginia with 9 specialties ranked among the best in the nation. - Our footprint encompasses 3 community hospitals and an integrated network of primary and specialty care clinics throughout Charlottesville, Culpeper, Northern Virginia, and beyond. The University of Virginia is an equal opportunity employer. All interested persons are encouraged to apply, including veterans and individuals with disabilities. Learn more about UVA’s commitment to non-discrimination and equal opportunity employment.
Role Description At Piedmont Healthcare, you’ll love a shared purpose, be motivated to be your best, and be recognized for your contributions. Piedmont Healthcare leaders are in your corner and invested in your success. Our wellness programs and comprehensive total benefits and rewards will meet your needs for today and help you plan for the future. - Reviewing clinical documentation to facilitate the accurate representation of the severity of illness, expected risk of mortality, and complexity of care. - Improving the quality of the physician's clinical documentation through extensive record review and interaction with: - Physicians - HIM/Coding professionals - Nursing staff - Case management - Collaborating with Coding professionals to educate the patient care team on changes in documentation guidelines and/or documentation deficiencies noted. - The patient care team includes but is not limited to: - Attending physicians - Consultants - Physician extenders - Allied health practitioners - Nursing - Case management - The Specialist reports to the Clinical Documentation Improvement Director. Qualifications - Associate’s Degree in nursing, Health Information Management or a related field - Required - Bachelor’s Degree - Preferred Requirements - 5 years of recent hospital experience/practice, preferably in an ICU, CCU or complex Med/Surg environment - Required - Previous clinical documentation improvement experience, utilization management, precertification, coding, Medicare regulations, quality assurance, or related area - Preferred - Prior experience with Epic - Preferred - Must have one of the following upon hire: - RN - Registered Nurse - Georgia State Licensure and/or NLC/eNCL Multistate Licensure - Required - CCS - Certified Coding Specialist - Required - RHIT - Registered Health Information Technician - Required - RHIA - Registered Health Information Administrator - Required - CCDS - Certified Cardiac Device Specialist - Required Company Description Piedmont Healthcare Corporate
Clinical Documentation Integrity Specialist – Lead
Quorum HealthEmpowering hospitals and healthcare providers in communities across the nation.
• The Clinical Documentation Integrity Specialist (CDIS) Lead is an advanced level position for the experienced and proficient CDI Specialist consistently meeting or exceeding all criteria for CDIS advanced performance. • The CDIS Lead provides support to CDI leadership within a defined scope of facilities and CDI team. • The CDIS Lead serves as a liaison between senior leadership, medical staff, nursing, coding, case management and quality departments. • Key Responsibilities: May be assigned special projects related to CDI processes, quality, data analysis, or HIM/CDI performance. • Assumes responsibility for daily workflow process and adjustments for the CDI team. • May present CDI performance metrics at facility meetings. • May present CDI education as needed. • Will assume operational oversight in the absence of the CDI Director. • Supports CDI team through multidisciplinary approach in support of program goals. • Facilitates collaborative efforts between CDI, HIM and Medical Staff providers. • Facilitates collaborative efforts between CDI and clinical teams such as Quality and Case Management. • Effectively utilizes leadership abilities and critical thinking skills to identify opportunities for team process and engagement optimization. • Maintains professional competency in documentation and coding practices by keeping up to date with new coding guidelines, policies/procedures, federal and state reimbursement.

