Job Description

3 days ago Be among the first 25 applicants This range is provided by SPECTRAFORCE. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $62.00/hr - $67.99/hr Direct message the job poster from SPECTRAFORCE Lead Recruiter (Pharma/Clinical) at SPECTRAFORCE Technologies Position Title: Principal Medical Writer Location: St. Paul, MN 55117 Duration: 6-12 months from the start date of the worker with a possibility to convert Work Schedule: Will be flexible after initial training period, likely hybrid schedule thereafter, to be worked out with the hiring manager Work Arrangement: Onsite role, transitioning to hybrid after initial training Position Summary: The Medical Writer on our Regulatory Clinical Evaluation team provides technical and strategic writing expertise throughout the product development and life cycle process. Daily activities are related to authoring Clinical Evaluation Reporting documents for Neuromodulation, CAHF, and Vascular products. For years, our organization’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring systems, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Every day, our technologies help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks. Key Responsibilities: 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. Evaluates and summarizes clinical evidence including data from sources such as clinical investigations, literature, post-market surveillance, risk, and post market clinical evaluations. Analyzes results in preparation for product applications and submissions. Collaborates with team members and stakeholders in planning for and supporting CER related projects and processes. Supports additional clinical, regulatory, quality and engineering related deliverable as assigned. Effectively communicates and collaborates with Sales and Marketing, R&D, Regulatory Affairs, Library Services, Product Performance Group (PPG), Quality Engineering, Clinical Affairs, Clinical Science, Risk Management and Medical Affairs in completing clinical evaluation project related deliverables. Maintains thorough knowledge of assigned products. Identifies appropriate sources of relevant data, interprets, evaluates and incorporates information from various sources including literature, clinical data, and medical references. Reviews IFUs, patient guides, Risk Management files, Clinical Evaluation Protocols, Clinical Evaluation Reports and Plans (CER/CEP), physician training materials, ensuring alignment of risk information. Involved in responses to complex queries such as those issued by notified bodies and stakeholders. Authors and contributes to necessary documents for regulatory submissions and communications, risk reviews and other processes such as regulatory inquiries. Ensures quality in all deliverables and documentation with attention to detail, consistency and integrity of data. Responsible for compliance with applicable corporate and divisional policies and procedures. Ensures compliance to applicable regulations and guidance’s (ISO13485, ISO14155, ISO14791, MEDDEV 2.7.1, MDR, and EU and FDA guidance documents) and applicable SOPs and DOPs. Qualification & Experience: Bachelor’s Degree or an equivalent combination of education and work experience. 6-8 years of medical writing experience in the medical or pharmaceutical industry or 8+ years general technical writing experience required. Experience may include writing experience in a medical, pharmaceutical, medical device, clinical research, medical or research industry, or combination of these skills. Biomedical, sciences, medicine or similar health-related discipline preferred. CER writing experience preferred. Excellent written and verbal communication skills. Experience with collaborative, cross-functional teams. Excellent analytical skills and ability to manage complex tasks and manage time effectively. Proficient with Word, Excel, PowerPoint, Outlook, etc. Notes: Medical Device MDR compliant CERs, CEPs, and SSCPs for Structural Heart and Neuromodulation Class III devices. Top 3 Skills or Any Specific type of Experience you are looking for: Experience writing Medical Device MDR compliant CERs, CEPs, and SSCPs. Structural Heart, Neuromodulation, or other medical device experience such as Clinical Study Management. Interview Process/Methods: 1) Phone Screen with HM, 2) In-Person and/or On-Camera interview with HM and 3 other persons. Seniority level Seniority level Mid-Senior level Employment type Employment type Contract Job function Job function Science and Engineering Industries Medical Equipment Manufacturing Referrals increase your chances of interviewing at SPECTRAFORCE by 2x Principal Medical Writer (Contract-to-Hire) Senior Medical Writer (Contract-to-Hire) Associate Director- Medical Science Liaison - Hematology and Theragnostic/Radioligand Therapies (Mid-West) Minneapolis, MN $200,000 - $250,000 6 days ago Eden Prairie, MN $80,000 - $100,000 3 weeks ago Medical Science Liaison (MSL), Medical Affairs - North Central Minneapolis, MN $160,000 - $220,000 4 hours ago Plymouth, MN $96,000 - $120,000 5 days ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr SPECTRAFORCE

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