Rédacteur scientifique principal en médecine
3 days ago
Fridley, MN, United States
Medtronic plc
Full-time
$108,000 - $162,000
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Rédacteur scientifique principal en médecineNous utilisons des cookies nécessaires et des cookies de mesure d’audience pour assurer le fonctionnement de ce site et produire des statistiques anonymes. Nous souhaitons également utiliser des cookies et des technologies similaires pour améliorer le fonctionnement du site, analyser de façon plus précise l’activité des visiteurs et afficher des publicités personnalisées. Nous définirons ces cookies et technologies uniquement si vous les acceptez. Vous pouvez revenir sur votre décision à tout moment en cliquant sur l’icône « Cookie » qui se trouve en bas à gauche de chaque page. Pour obtenir plus d’informations sur les cookies de notre site et sur les tiers qui les placent, cliquez sur « Préférences en matière de cookies ».### Rédacteur scientifique principal en médecinePostuler: Sur site: Fridley, Minnesota, United States of America: Temps plein: Offre publiée hier: Date de fin : 14 novembre 2026 (Il reste 15 jour(s) pour postuler): R80673We anticipate the application window for this opening will close on
- 14 Nov 2026Chez Medtronic, vous pouvez entamer une longue carrière d’exploration et d’innovation tout en aidant à soutenir l’accès aux soins de santé et l’équité pour tous. Vous dirigerez avec détermination en surmontant les obstacles à l’innovation dans un monde davantage connecté et compatissant.Journée typeThe Neuromodulation operating unit develops therapies for chronic pain, movement disorders, and nervous system conditions through spinal cord stimulation (SCS), and targeted drug delivery technologies. The Clinical Evidence function generates and disseminates clinical and scientific evidence to support product adoption, regulatory requirements, reimbursement initiatives, and evidence-based decision making across the business. This position is based onsite in Rice Creek/Fridley, Minnesota, with an expectation of working onsite four days per week. The role requires approximately 10% travel to support cross-functional collaboration, investigator engagement, and evidence-generation activities. The Senior Clinical Evidence Specialist supports the development, evaluation, and communication of clinical evidence for Neuromodulation therapies. This role partners with physicians and cross-functional stakeholders to advance scientific publications, assess evidence gaps, support evidence strategies, and ensure the accuracy and quality of clinical and scientific communications. Primary Responsibilities* Develop, author, and submit scientific manuscripts, abstracts, posters, podium presentations, and clinical evidence reports.
* Conduct literature reviews and synthesize scientific data to support evidence generation, publication activities, and business objectives.
* Lead or support medical evidence assessments and evidence gap analyses to inform clinical and evidence strategies.
* Collaborate with physicians, investigators, and healthcare professionals on publication development and scientific communications.
* Partner with Marketing, Medical Affairs, Reimbursement, Regulatory Affairs, Research and Development, and Clinical teams to provide clinical evidence expertise.
* Review clinical and scientific content for accuracy, including marketing and educational materials.
* Support investigator meetings, advisory boards, and external research collaborations.
* Maintain publication and literature databases and support responses to regulatory, audit, or submission-related inquiries. Required Qualifications* Bachelor's degree with 4+ years of experience in clinical research, scientific publications, clinical studies, or program management OR advanced degree with 2+ years of experience in clinical research, scientific publications, clinical studies, or program management.
* Experience authoring or contributing to scientific manuscripts, abstracts, clinical reports, or evidence-based communications.
* Experience conducting literature reviews, evidence assessments, or scientific data analyses.
* Experience collaborating with cross-functional stakeholders in a matrixed environment.
* Experience supporting regulated clinical research activities within the medical device, pharmaceutical, biologic, or healthcare industry. Preferred Qualifications* Experience writing clinical study plans, clinical study reports, clinical evaluation reports, scientific manuscripts, or clinical evidence reports.
* Record of leading scientific publications and serving as an author on peer-reviewed publications.
* Knowledge of International Committee of Medical Journal Editors (ICMJE) guidelines and Good Publication Practices.
* Knowledge of clinical research study design, Good Clinical Practice (GCP), U.
S. Food and Drug Administration (FDA), International Council for Harmonisation (ICH), or global clinical regulations.
* Experience supporting neurology, psychiatry, neuromodulation, pain management, or related therapeutic areas.
Pour les diplômes de baccalauréat o
- 14 Nov 2026Chez Medtronic, vous pouvez entamer une longue carrière d’exploration et d’innovation tout en aidant à soutenir l’accès aux soins de santé et l’équité pour tous. Vous dirigerez avec détermination en surmontant les obstacles à l’innovation dans un monde davantage connecté et compatissant.Journée typeThe Neuromodulation operating unit develops therapies for chronic pain, movement disorders, and nervous system conditions through spinal cord stimulation (SCS), and targeted drug delivery technologies. The Clinical Evidence function generates and disseminates clinical and scientific evidence to support product adoption, regulatory requirements, reimbursement initiatives, and evidence-based decision making across the business. This position is based onsite in Rice Creek/Fridley, Minnesota, with an expectation of working onsite four days per week. The role requires approximately 10% travel to support cross-functional collaboration, investigator engagement, and evidence-generation activities. The Senior Clinical Evidence Specialist supports the development, evaluation, and communication of clinical evidence for Neuromodulation therapies. This role partners with physicians and cross-functional stakeholders to advance scientific publications, assess evidence gaps, support evidence strategies, and ensure the accuracy and quality of clinical and scientific communications. Primary Responsibilities* Develop, author, and submit scientific manuscripts, abstracts, posters, podium presentations, and clinical evidence reports.
* Conduct literature reviews and synthesize scientific data to support evidence generation, publication activities, and business objectives.
* Lead or support medical evidence assessments and evidence gap analyses to inform clinical and evidence strategies.
* Collaborate with physicians, investigators, and healthcare professionals on publication development and scientific communications.
* Partner with Marketing, Medical Affairs, Reimbursement, Regulatory Affairs, Research and Development, and Clinical teams to provide clinical evidence expertise.
* Review clinical and scientific content for accuracy, including marketing and educational materials.
* Support investigator meetings, advisory boards, and external research collaborations.
* Maintain publication and literature databases and support responses to regulatory, audit, or submission-related inquiries. Required Qualifications* Bachelor's degree with 4+ years of experience in clinical research, scientific publications, clinical studies, or program management OR advanced degree with 2+ years of experience in clinical research, scientific publications, clinical studies, or program management.
* Experience authoring or contributing to scientific manuscripts, abstracts, clinical reports, or evidence-based communications.
* Experience conducting literature reviews, evidence assessments, or scientific data analyses.
* Experience collaborating with cross-functional stakeholders in a matrixed environment.
* Experience supporting regulated clinical research activities within the medical device, pharmaceutical, biologic, or healthcare industry. Preferred Qualifications* Experience writing clinical study plans, clinical study reports, clinical evaluation reports, scientific manuscripts, or clinical evidence reports.
* Record of leading scientific publications and serving as an author on peer-reviewed publications.
* Knowledge of International Committee of Medical Journal Editors (ICMJE) guidelines and Good Publication Practices.
* Knowledge of clinical research study design, Good Clinical Practice (GCP), U.
S. Food and Drug Administration (FDA), International Council for Harmonisation (ICH), or global clinical regulations.
* Experience supporting neurology, psychiatry, neuromodulation, pain management, or related therapeutic areas.
Pour les diplômes de baccalauréat o
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Fridley, MN, United States Medtronic plc Full-time $108,000 - $162,000Medtronic's Neuromodulation division is seeking a Senior Clinical Evidence Specialist onsite in Fridley, MN. The role focuses on developing clinical evidence for neuromodulation therapies, advancing publications, and supporting evidence strategies.Expect ~10% travel and close collaboration with physicians and cross-functional teams to ensure accurate,...