Medtronic

Healthcare

ClinicalResearchSpecialist-ExternalResearchProgram(ERP)

€53–79k Maastricht, Limburg, Netherlands FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Clinical Research Specialist- External Research Program (ERP) at Medtronic. Skills: External research program, Investigator-initiated studies, Clinical research. Support execution of External Research Program portfolio. Serve as operational point of contact”

Industry & Context.

Healthcare
Problems you'll solve

Creative problem solving

What They're Looking For.

Must Have

Bachelors in biological science or biomedical engineering, Experience in clinical or laboratory research, Worked in a clinical cardiac setting, Detail oriented, Comfortable presenting to small audiences, Ability to influence colleagues, English fluency

Nice to Have

Master's degree in biological science or biomedical engineering, Additional languages, Aptitude for creative problem solving, Scientific background in Cardiac Rhythm Management, Customer-facing background in Cardiac Rhythm Management

What You'll Do.

Support execution of External Research Program portfolio

Serve as operational point of contact

Coordinate ERP lifecycle activities

Partner with cross functional stakeholders

Facilitate review of ERP proposals

Support ERP agreements and amendments

Lead financial management of portfolio

Process payment requests

Communicate with cost center owners

Monitor study progress

Identify documentation gaps

Conduct portfolio reviews

Liaise on fair market value evaluation

Liaise on contracting

Align terms with operational requirements

Align terms with compliance requirements

Contribute to continuous improvement of ERP tools

Contribute to continuous improvement of ERP templates

Contribute to continuous improvement of ERP workflows

Share learnings across clinical organization

Share best practices across clinical organization

Share learnings across enterprise ERP community

Share best practices across enterprise ERP community

Embrace responsible hyperautomation use

Embrace responsible AI use

Operate with a global mindset

Support ERPs in various countries

Keep in mind cultural norms

Keep in mind cultural expectations

Build optimal relationships

Maintain optimal relationships

Foster effective collaborations

How You'll Work.

Team & Collaboration

Cross functional stakeholders; Medical scientific advisors; Local clinical teams; Internal and external parties

Communication Scope

Presenting to physicians

Full Job Description

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. # **A Day in the Life** Seeking a dynamic individual interested in advancing the cardiac rhythm management (CRM) operating unit (OU) via support of our external research program (ERP). Ideal role for a candidate that has a keen interest in investigator-initiated research operations on a global scale, with room to grow into some scientific responsibility in the future. **Responsibilities may include the following and other duties may be assigned:** * Support execution of the External Research Program (ERP) portfolio by serving as an operational point of contact for investigator initiated studies and coordinate ERP lifecycle activities (from review through close out) in alignment with Medtronic ERP policy and applicable procedures, ensuring documentation, timelines, and milestones are tracked appropriately * Partner with cross functional stakeholders (e.g., R&T, Clinical, Legal, Compliance, and Finance, etc.) to facilitate review and support of ERP proposals, agreements, and amendments * Lead effective financial management of portfolio, inclusive of forecasting, payment requests, accruals, and proactive communication to cost center owners/stakeholders * Monitor study progress through appropriate tracking tools, proactively identifying risks, data or documentation gaps, and escalating issues per defined processes and conduct routine portfolio reviews with medical scientific advisors, and/or local clinical teams to align on study progress, status, and any watch outs * Liaise with local team or MCRS on fair market value evaluation and contracting, aligning agreed upon terms with operational and compliance requirements and contribute to continuous improvement of ERP tools, templates, and workflows, sharing learnings and best practice

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