Clinical Research

• You will bridge the gap between strategy and execution across the entire trial lifecycle—from early development to late-stage delivery—ensuring our clinical assets are executed with maximum speed, efficiency, and clinical quality.
• Develops and executes country-level site engagement strategies aligned with internal priorities.
• Conducts early, strategic landscaping and site engagement during the protocol concept and study set-up phases to identify optimal sites.
• Builds deep, multi-stakeholder relationships at strategic sites.
• Serves as the local escalation point for study challenges.
• Partners seamlessly with internal teams and CROs to ensure unified site communication.
• Manages assigned local/global clinical studies by overseeing CRO performance and mitigating timeline or operational risks.
• Focus on driving adoption of DCT and digital solutions with our sites.

Clinical Research Engagement Lead – Central Region

• Provides leadership for the conduct of clinical studies and for the regulatory affairs function as it applies to product approval
• Develops and implements regulatory strategies to obtain timely product approvals from worldwide regulatory bodies
• Ensures regulatory submissions are accurately prepared and comply with regulatory approvals
• Represents Medtronic from a clinical research perspective within the country / region and also collects feedback from local customers and authorities
• Builds and maintains a strong network and close relationship with the various internal and external parties
• Leads execution for both local and global studies, manages clinical research projects over all of the Medtronic therapies across multiple businesses

Senior Clinical Research Director – CRDN

• Conduct clinical studies according to FDA/GCP and ICH regulations and guidelines.
• Provide medical care to patients, always ensuring patient safety comes first.
• Schedule subject visits within protocol windows, ensuring scheduling capacity is maximized.
• Perform all defined study activities (i.e., informed consent, screening, and protocol procedures which include but are not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.).
• Record all patient information and results from tests as per protocol on required forms.
• Where required, may complete IP accountability logs and associated information.
• Reports suspected non-compliance with relevant site staff.
• Ensures that IRB approval is obtained prior to study initiation and IRB requirements are met throughout the study.
• Promotes the company and builds a positive relationship with patients to ensure retention.
• Attend site initiation meetings and all other relevant meetings to receive training on protocol.
• May be required to call patients, do patient bookings and follow-up calls to confirm bookings or provide information or results.
• Logs/complete information on sponsor systems and ensures all information provided is accurate (i.e., case report forms, EDC, etc.) and ensures it is completed within timeframe.
• Gather and maintain source documents, updates patient files and notes, always ensuring relevant and most up to date information is recorded.
• Adhere to company COP/SCOP.
• May be required to dispose of waste according to standards and assist in keeping a general neat appearance of the facility.

Traveling Clinical Research Coordinator II

• Serve as the Clinical Research representative on New Product Development (NPD) core teams, acting as the primary clinical voice throughout the product lifecycle—from concept through post-market evaluation
• Develop and lead clinical evidence strategies aligned to regulatory, medical, and commercial objectives, including identification of evidence gaps necessary to support safety, performance, and claims
• Critically evaluate and synthesize clinical literature and competitive evidence landscapes to inform product development decisions, clinical positioning, and differentiation strategy
• Lead and influence clinical study design, including protocol development, endpoint selection, and overall evidence generation approach to support intended use and global market needs
• Provide clinical oversight, review, and approval of product claims to ensure alignment with scientific evidence, regulatory requirements, and reimbursement strategies
• Partner cross-functionally (R&D, Regulatory, Marketing, Medical Affairs, Quality) to integrate clinical insights into product requirements, risk management, and benefit-risk assessments
• Drive development of key clinical deliverables, including Clinical Evaluation Plans/Reports, Clinical Study Reports, and other documentation supporting regulatory submissions and product commercialization
• Synthesize clinical data to support regulatory approval, evidence dissemination, and lifecycle management activities
• Identify and proactively manage clinical and patient-related risks early in development, contributing to mitigation strategies and overall product safety profile
• Influence Voice of Customer (VoC) translation and ensure clinical insights are reflected in product design, usability, and intended use

Principal Clinical Research Specialist

• Working cross-functionally to conduct gap analyses in clinical evidence and recommending strategies in line with business goals
• Providing leadership for the conduct of clinical research for product approval, post-market clinical follow-up, and market adoption or development
• Ensuring research plans are scientifically valid, meeting regulatory requirements, and are conducted within ethical guidelines
• Ensuring audit readiness and participating in related activities, e.g., serving as a subject matter expert
• Setting and communicating strategy, direction, priorities, and goals in partnership with the CRMS Leadership Team
• Serving as the ENT Clinical Research representative for enterprise councils and communities of practice
• Creating and maintaining a culture of ownership and accountability
• Managing performance, developing talent, and fostering engagement and inclusion through 1:1s, feedback, coaching, and delegation
• Setting and maintaining the budget and resourcing for the clinical research program and team
• Advancing ways of working and operational efficiency, including the use of AI-enabled tools
• Communicating business and operational developments up, down, and across
• Preparing reports and presentations for internal and external stakeholders for projects and budgets, integrating information from multiple sources

Senior Clinical Research Manager

• Lead scientific activities associated with the design, conduct, and reporting of clinical trials
• Participate in the development of clinical evidence to establish feasibility
• Achieve regulatory approvals and meet ongoing regulatory requirements
• Gain reimbursement and support full commercial adoption of medical devices
• Support the analysis and interpretation of scientific data
• Write clinical study protocols, reports, and scientific publications
• Aid in the production of additional study-level documents
• Interact with physician Key Opinion Leaders and various cross-functional teams
• Interact with global regulatory agencies to obtain market approval of new products

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Clinical Research Engagement Lead – Central Region

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