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Clinical Evaluator (CER Writer)
Clinical Evaluator (CER Writer)Experis • WROCŁAW, Dolnoslaskie
Clinical Evaluator (CER Writer)

Clinical Evaluator (CER Writer)

Experis • WROCŁAW, Dolnoslaskie
16 dni temu
Opis pracy

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Location : 100% remote work

Salary : 15 300 – 17 000 PLN gross per month (temporary employment contract via Experis)

Tasks :

  • Writes and contributes to Clinical Evaluation reporting deliverables including Clinical Evaluation Plans / Reports, PMS and PMCF Plans / Reports, SSCPs, Regulatory Responses and other related documentation
  • Effectively communicates and collaborates with global R&D, Regulatory Affairs, Library Services, Quality, Clinical Affairs, and Risk Management teams in completing clinical evaluation project deliverables and publication reviews
  • Maintains thorough knowledge of assigned products and identifies appropriate sources of relevant data
  • Interprets, evaluates and incorporates information from literature, clinical data and medical references
  • Manages document control and reviewers for CERs
  • Ensures quality, consistency and integrity of data in all deliverables
  • Ensures compliance with applicable regulations and guidance documents including ISO13485, ISO14155, ISO14791, MEDDEV 2.7.1, MDR, EU and FDA guidance documents and applicable SOPs
  • Demonstrates understanding of clinical background and state of the art, literature review and search strategy, article processing and synthesis, MAUDE search and safety database summary, internal clinical trial results and clinicaltrials.gov search
  • Integrates and interprets competitor data, sales and complaints analysis, vigilance summary, risk / benefit evaluation, claims matrix analysis, field actions, CAPAs, recalls, mitigations, references, appendices and QC processes with MD Reviewer and Notified Bodies
  • Maintains CER SOP for current MDR regulatory requirements
  • Supports research for Post Market Surveillance Reports

Requirements :

  • Bachelor’s degree in a science or equivalent technical degree or equivalent combination of education and experience
  • Minimum 3 years of relevant experience with Medical Device CERs
  • Excellent written and verbal communication skills in English
  • Strong analytical and project management skills
  • Ability to develop spreadsheets or databases for metrics capture, assembly and graphical presentation
  • Advanced scientific or medical degree considered a plus
  • Medical Device PMS experience preferred
  • Experience in experimental design, data interpretation and summarizing clinical data
  • Knowledge of consumer product regulations and / or quality systems
  • 3+ years of medical writing experience in medical device or pharmaceutical industry or 7+ years of technical writing
  • Experience writing, editing and managing clinical and technical documentation for new and existing products
  • Experience in medical, pharmaceutical, medical device, clinical research or related industries
  • Excellent analytical skills and ability to manage complex tasks and time effectively
  • Proficiency in Word, Excel, PowerPoint, Outlook
  • Experience working in a cross functional global environment
  • MDR audit exposure
  • Ability to work remote in Poland
  • Offer :

  • Multisport card
  • Private healthcare
  • Access to an e learning platform
  • Group life insurance
  • header-over-companydesc

    Experis to światowy lider rekrutacji specjalistów i kadry zarządzającej w kluczowych obszarach IT. Z nami znajdziesz konkurencyjne oferty zatrudnienia oraz ciekawe projekty IT skierowane zarówno do ekspertów z wieloletnim doświadczeniem, jak i osób, które dopiero zaczynają swoją przygodę w branży IT.job-detail-footer

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