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Sr. Clinical Evaluation Medical Writer

Integrated Resources, Inc

Mounds View, MN

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JOB DETAILS
JOB TYPE
Contractor
SKILLS
Cardiac Monitoring, Clinical Assessment, Clinical Best Practices, Clinical Data, Clinical Medicine, Clinical Outcomes, Clinical Research, Clinical Support, Clinical Trial, Coaching, Cross-Functional, Data Analysis, Document Management, Documentation Format, Drug Development, Editing, Healthcare Quality, Marketing, Medical Writing, Mentoring, Negotiation Skills, Options Analysis, People Management, Policy Development, Procedure Development, Process Improvement, Product Safety, Product Testing, Project/Program Management, Proofreading, Regulations, Regulatory Compliance, Regulatory Requirements, Requirements Management, Research & Development (R&D), Risk, Risk Analysis, Risk Management, Schedule Development, Strategic Planning, Technical Analysis, Technical Writing, Time Management
LOCATION
Mounds View, MN
POSTED
Today
Title: Sr. Clinical Evaluation Medical Writer Location: Mounds View, MN (Hybrid- 4 Days Onsite) Duration: 24 Months+ Possible Extension Top Needs: 1. Clinical Evaluation experience (end to end would be ideal) 2. Experience with cardiac rhythm management devices (ideal) 3. Experience with literature management tools (ReadCube is ideal) Job Description: This role is responsible for analyzing and integrating diverse clinical evidence to evaluate product safety and performance and identify potential data gaps or risks. The position leads and supports clinical evaluations in compliance with applicable global regulatory requirements, working closely with crossfunctional stakeholders to define clinical evaluation strategies and support regulatory interactions. The role requires maintaining current knowledge of clinical evaluation best practices and the evolving clinical and regulatory landscape, and producing clear, accurate, and highquality clinical documentation. Responsibilities also include supporting risk/benefit and stateoftheart assessments, managing document timelines, addressing regulatory feedback, and providing guidance or mentoring to colleagues as needed. Education Required: Years Experience Required: Bachelors degree with a minimum of 4 years of experience in clinical research/clinical evaluation/clinical evidence, or advanced degree with a minimum of 2 years of experience in clinical research/clinical evaluation/clinical evidence Responsibilities may include the following and other duties may be assigned. Identify, compile and analyze multiple data types (clinical investigation results, literature and clinical experience, preclinical data, etc.) in order to evaluate product safety and performance and identify potential evidence gaps Collaborate, plan and develop clinical evaluations in accordance with relevant guidelines/regulations (i.e. CERs, clinical dossiers) with stakeholders from multiple functions and in compliance with applicable standards and in alignment with business needs Develop and maintain therapeutic and device operation knowledge; apply this knowledge to the development of well-written, clear and concise reports Identify potential evidence gaps or risks to existing data and work with stakeholders to assess options, track, and communicate risks as needed Develop search strategies to identify and obtain existing, relevant data (internal or external) Stay current on clinical evidence landscape and provide guidance to teams on sufficient data Develop and maintain in-depth knowledge of clinical evaluation best practices and regulatory agencies guidelines on clinical evaluation requirements Assess other technical file documents aProductst clinical data, available current literature and industry state of the art (this may include risk management plans, IFU, etc.) Collaborate with other functional groups (R&D, clinical, quality, marketing, etc.) to conduct risk/benefit assessments and evaluate State of the Art for the therapy area and product line Conduct proofreading, editing, document formatting, review comment integration and document completion / approval activities Address deficiencies and or answer questions from regulatory agencies as needed Work in close collaboration with cross-functional stakeholders to determine appropriate clinical evaluation strategy; may provide input to clinical trial design Interface with regulators and may lead discussions and develop strategies with cross functional stakeholders to negotiate and influence regulatory reviewers on the clinical evaluation Provide guidance, mentoring and coaching to colleagues Create and manage project schedule for each document May lead the development of policies, procedures, and/or process improvement initiatives for the group or clinical department

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Integrated Resources, Inc