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Medical Records Jobs in Massachusetts

Sr. Medical Writer

Integrated Resources, Inc

Mansfield, Massachusetts

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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Adobe Illustrator, Adobe Photoshop, Analysis Skills, Biology, Biotech and Pharmaceutical, Clinical Assessment, Clinical Outcomes, Clinical Research, Clinical Trial, Data Entry, Documentation, Drug Development, Editing, Graphics Software, Healthcare, Information Technology & Information Systems, Interpersonal Skills, Mail Processing, Marketing, Medical Equipment, Medical Writing, Microsoft Excel, Microsoft Office, Microsoft PowerPoint, Microsoft Word, Nursing, Organizational Skills, Product Reviews, Publications, Regulations, Regulatory Requirements, Rehabilitation Nursing, Reporting Skills, Research & Development (R&D), Risk Management, Sales, Science Software, Scientific Publications, Scientific Research, Support Documentation, Surveillance, The Joint Commission (TJC), Work From Home
LOCATION
Mansfield, Massachusetts
POSTED
Today
Sr. Medical WriterIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionTitle: Sr. Medical WriterDuration: 2 yearsLocation: Mansfield, MA 02048 (100% possibility of relocation)Summary of position:The Medical Writer is responsible for the preparation of documents that support the presentation, publication needs of assigned therapeutic areas and/or products in the Covidien Scientific Communications group.Remote candidates are an option. Local candidate to Mansfield, MA preferred.Essential functions:This role predominantly focuses on writing, editing and reviewing regulatory (e.g. Clinical Evaluation Reports/clinical study reports/summaries) documents and responses to Notified Bodies.Post Market Surveillance activities (monthly literature review of our product)Scientific Writing e.g. abstracts, manuscripts, presentationsRequires a strategic understanding of the therapeutic areas, business and study objectives as well as statistical dataIndependently, critically writes and edits scientifically complex documents for substantial intellectual contentReviews and provides input on the data being considered for publication to ensure alignment with current medical issues and corporate goalsExpert knowledge of clinical research, device/drug development processes, regulatory requirements, and good clinical practicesAbility to understand and interpret statistical results of clinical studies; ability to summarize complex results and present them in a clear, concise, and scientifically accurate manner to a wide range of audiencesNon-essential functions:1. Other duties as assigned with or without accommodation.Minimum requirements:Clinical, scientific or research backgroundPh.D./Pharm.D plus 1 to 2 years of related pharmaceutical/medical device industry experience(e.g., medical writing, clinical research)BS, B. Pharm, MS, plus 4 to 6 years of relevant pharmaceutical/medical device industry experienceExperience in Medical WritingCommunication/Presentation SkillsExcellent Interpersonal RelationshipsExpert understanding of scientific or clinical research and the scientific methodDemonstrated scientific writing abilityMust be highly proficient in the use of Microsoft Office suite (especially Microsoft Word and PowerPoint); skill in Microsoft Excel, Photoshop, Illustrator, EndNote Reference Software, and other scientific graphics software would be helpfulGood understanding of statistical methodsOther Skills:Organizational relationships/scope:The Medical Writer will report to the Sr. Director of Scientific Communications. This position will meet and communicate regularly with Clinical Affairs, PACE, R&D, marketing, Sales, KOL's and others as necessary to build and collaborateQualificationsSpecial Notes:100% remote work is possible, on site is preferredPHD with 5+ years of experience or Nurses with 10+ years of experience is requiredThe Medical Writer has to review the post market surveillance data, has to create a demonstration of safety reportsExtensive experience with Clinical Evaluation Report is required, person has to be able analyze complex scientific informationPost Marker Surveillance experience is requiredGood understanding of risk management and hands on experience with risk management documentation is requiredAdditional InformationKind Regards,Sabanaaz ShaikhClinical RecruiterIntegrated Resources, Inc.IT Life Sciences Allied Healthcare CROGold Seal JCAHO Certified for Health Care Staffing"INC 5 0 0 0 's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)

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