Clinical Evidence Planning & Evaluations Manager

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We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions.

This person will create and drive clinical evidence strategies, develop clinical evaluation plans and reports, and provide clinical input across regulatory and product management teams.

Post-market clinical follow-up activities and clinical review of promotional materials are also key responsibilities.

This is remote role in the US and Canada with less than 25% travel requirements

This is a role well suited for a self-driven professional looking to expand the impact of Medical Affairs work across the organization.

As a Clinical Evidence Planning and Evaluations Manager, you will be responsible for:


* Creating and driving the Clinical Evidence Strategy for Varian's devices


* Creation of Clinical Evaluation Plans, Reports, and Post-Market Clinical Evaluation Plans, and Reports (CEP/CER and PMCFP/PMCFR)


* Providing clinical perspective and input to cross-functional teams regarding clinical development, risk management, product management, and post-market surveillance


* Execute Post-Market Clinical Follow Up activities (may include customer surveys, annual literature searches, clinical studies)


* Provide clinical review of promotional material and claims in support of publishing customer facing content

This position may suit you best ifyou are familiar with what is below, and would like to develop your skills with Healthineers:


* You have familiarity with design and manufacture medical devices, especially those used in the radiation oncology setting


* You have exemplary technical writing and verbal communication skills


* You prefer an autonomous working environment, as this position is remote.

Required skills and education to have for the success of this role


* Understanding of Clinical Evaluation and Post Market Clinical Follow Up Requirements of class I-III medical devices as designated in the European Union Medical Device Regulation (EU MDR)


* Master's or PhD in Medical Physics (preferred), Biophysics, Biomedical Engineering.

Other degree programs considered based on experience


* 3-5 years' experience with clinical evaluations, medical physics, or related field.

At Siemens Healthineers, we value those who dedicate their energy and passion to a greater cause.

Our people make us unique as an employer in the med-tech industry.

What unites and motivates our global team is the inspiration of our common purpose: To innovate for healthcare, building on our remarkable legacy of pioneering ideas that translate into even better healthcare products and services.

We recognize that taking ownership of our work allows both us an...