Clinical Job Opening: Remote Medical Role at Siemens Healthineers | Apply Now
A remote clinical job opportunity is now open for professionals looking to expand their impact in Medical Affairs. Siemens Healthineers jobs offer a dynamic environment where clinical evaluation, post-market clinical follow-up, and cross-functional collaboration come together to drive innovation in healthcare. This medical job is ideal for self-driven professionals seeking flexibility, global exposure, and meaningful work.
Job Details:
- Job Title: Clinical Evaluation Specialist-2
- Type: Remote
- Locations: PUN MA
- Time Type: Full-time
- End Date: March 9, 2026
- Job Requisition ID: R-26419
About the Company
At Siemens Healthineers, people dedicate their energy and passion to a greater cause. As a global leader in medical technology, Siemens Healthineers employs more than 72,000 people across over 70 countries. The organization continuously pushes boundaries to create better outcomes and experiences for patients through innovative healthcare products and services.
Job Description
This medical job is well-suited for a self-driven professional looking to expand the impact of Medical Affairs work across the organization. As a Clinical Evaluation Specialist, focus areas include execution of clinical evaluation and post-market clinical follow-up activities while providing clinical input across multiple functions. This clinical job is fully remote and offers flexibility to support global teams.
Qualifications
- Familiarity with medical devices used in the field of radiation or interventional oncology
- Basic understanding of EU MDR and related guidance documents related to Clinical Evaluations and Post-Market Clinical Follow-Up
- Familiarity with data analysis (e.g., literature appraisal, survey data) and statistical methods
- Exemplary medical writing and verbal communication skills
- Ability to work autonomously in a remote job environment
- 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 Science or a Medical field; Medical Physics, Biophysics, or Biomedical Engineering preferred
- At least 2 years’ experience with clinical evaluations, medical writing, medical physics, or related field
- Advanced knowledge of Microsoft Office, Word, and Excel; experience with reference manager software preferred
Key Responsibilities
- Execution of Clinical Evaluation and Post-Market Clinical Follow-up support activities (may include customer surveys, literature searches, clinical studies)
- Support creation of Clinical Evaluation Plans/Reports and Post-Market Clinical Follow-up Plans/Reports (CEP/CER and PMCFP/PMCFR)
- Provide clinical perspective and input to cross-functional teams such as risk management, product management, and post-market surveillance
- Provide clinical review of promotional material and claims in support of publishing customer-facing content
- Other duties, as assigned
