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Clinical Evaluation Writer Jobs (NOW HIRING)

$134K - $184K/yr

Creation of Clinical Evaluation Plans, Reports, and Post-Market Clinical Evaluation Plans, and ... You have exemplary technical writing and verbal communication skills * You prefer an autonomous ...

New

Strong experience in protocol development, writing clinical sections of documents for regulatory submission and clinical evaluation report writing * Ability to learn quickly and self-educate on ...

Clinical Evaluator

$80K - $100K/yr

Clinical Evaluators also generate thorough, timely documentation that ensures a smooth and intentional handoff to the care team, supported by AI note-writing tools. They provide feedback to the Tech ...

Strong experience in protocol development, writing clinical sections of documents for regulatory submission and clinical evaluation report writing * Ability to learn quickly and self-educate on ...

Medical Writing Specialist Division: Strategic Medical Affairs Reports To: Medical Safety Project ... Clinical Evaluation Reports (CERs), clinical data reports or summaries) documents and responses to ...

Experience writing Clinical Evaluation Plans and Reports (CEP, CER, respectively) to support EU MDD and MDR requirements. * Expertise in conducting focused literature searches on PubMed, Embase ...

Experience writing Clinical Evaluation Plans and Reports (CEP, CER, respectively) to support EU MDD and MDR requirements. * Expertise in conducting focused literature searches on PubMed, Embase ...

Experience writing Clinical Evaluation Plans and Reports (CEP, CER, respectively) to support EU MDD and MDR requirements. * Expertise in conducting focused literature searches on PubMed, Embase ...

Experience writing Clinical Evaluation Plans and Reports (CEP, CER, respectively) to support EU MDD and MDR requirements. * Expertise in conducting focused literature searches on PubMed, Embase ...

Experience writing Clinical Evaluation Plans and Reports (CEP, CER, respectively) to support EU MDD and MDR requirements. * Expertise in conducting focused literature searches on PubMed, Embase ...

Knowledge of regulatory requirements relative to medical devices including Clinical Evaluation Reports and Post Market Requirements * Ability to write and edit quality medical abstracts, white papers ...

Experience writing Clinical Evaluation Plans and Reports (CEP, CER, respectively) to support EU MDD and MDR requirements. * Expertise in conducting focused literature searches on PubMed, Embase ...

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Clinical Evaluation Writer information

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$54

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How much do clinical evaluation writer jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for clinical evaluation writer in the United States is $54.35, according to ZipRecruiter salary data. Most workers in this role earn between $39.90 and $64.18 per hour, depending on experience, location, and employer.

What is a clinical evaluation writer?

A Clinical Evaluation Writer is responsible for preparing clinical evaluation reports (CERs) and related regulatory documentation for medical devices. They analyze clinical data, review scientific literature, and ensure compliance with regulatory requirements like MDR (Medical Device Regulation) and FDA guidelines. Their work supports the safety and performance claims of medical devices for market approval. Strong writing, research, and regulatory knowledge are essential skills for this role.

What are the typical daily responsibilities of a clinical evaluation writer?

As a Clinical Evaluation Writer, your typical day involves conducting in-depth literature searches, critically appraising clinical data, and drafting or updating clinical evaluation reports (CERs) for medical devices or products. You'll frequently collaborate with regulatory teams, subject matter experts, and clinical professionals to gather and verify data, ensuring all documentation aligns with current regulatory requirements. Managing deadlines, responding to feedback from internal reviewers, and keeping up with changing regulations are also key parts of the job. This role requires a blend of independent research, technical writing, and teamwork to ensure timely and accurate regulatory submissions.

What are the key skills and qualifications needed to thrive as a clinical evaluation writer?

To thrive as a Clinical Evaluation Writer, you need a solid background in medical writing, regulatory affairs, and scientific literature analysis, usually supported by a degree in life sciences or a related field. Familiarity with tools like EndNote, document management systems, and knowledge of regulatory frameworks such as MDR/IVDR and MEDDEV 2.7/1 are typically required. Strong attention to detail, critical thinking, and the ability to communicate complex information clearly are key soft skills for success. These qualities ensure that clinical evaluation documents are accurate, compliant, and effectively support product submissions to regulatory authorities.

What does a clinical evaluation writer do?

A clinical evaluation writer creates detailed reports assessing the safety and performance of medical devices based on clinical data. They analyze study results, ensure compliance with regulatory standards, and often use tools like medical writing software to produce clear, accurate documentation.
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Cities with the most Clinical Evaluation Writer job openings:

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What states have the most Clinical Evaluation Writer jobs?

States with the most job openings for Clinical Evaluation Writer jobs include:

Infographic showing various Clinical Evaluation Writer job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $113,048 per year, or $54.4 per hour.

Clinical Evidence Planning & Evaluations Manager

Siemens Healthineers

Remote

$134K - $184K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New


Siemens Healthineers rating

8.4

Company rating: 8.4 out of 10

Based on 89 frontline employees who took The Breakroom Quiz

99th of 491 rated machine equipment manufacturers


Job description

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably.
Our inspiring and caring environment forms a global community that celebrates diversity and individuality. 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 and the company to grow. We offer you a flexible and dynamic environment and the space to move beyond your comfort zone to grow both personally and professionally.

#LI-Remote

Who we are: We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways.

How we work: When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual's potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world's most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

To find out more about Siemens Healthineers businesses, please visit our company page here.

The base pay range for this position is:

$134,300 - $184,668

Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.

If this is a commission eligible position the commission eligibility will be in accordance with the terms of the Company's plan. Commissions are based on individual performance and/or company performance.

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan. life insurance, long-term and short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time.

Equal Employment Opportunity Statement: Siemens Healthineers is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law.

EEO is the Law: Applicants and employees are protected under Federal law from discrimination. To learn more, click here.

Reasonable Accommodations: Siemens Healthineers is committed to equal employment opportunity. As part of this commitment, we will ensure that persons with disabilities are provided reasonable accommodations.

If you require a reasonable accommodation in completing a job application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please fill out the accommodations form here. If you're unable to complete the form, you can reach out to our HR People Connect People Contact Center for support at peopleconnectvendorsnam.func@siemens-healthineers.com. Please note HR People Connect People Contact Center will not have visibility of your application or interview status.

California Privacy Notice: California residents have the right to receive additional notices about their personal information. To learn more, click here.

Export Control: "A successful candidate must be able to work with controlled technology in accordance with US export control law." "It is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations."

Data Privacy: We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. We ask instead that you create a profile in our talent community where you can upload your CV. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you an alert when relevant positions become open. Register here to get started.

Beware of Job Scams: Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons that are currently posing as Siemens Healthineers recruiters/employees. These scammers may attempt to collect your confidential personal or financial information. If you are concerned that an offer of employment with Siemens Healthineers might be a scam or that the recruiter is not legitimate, please verify by searching for the posting on the Siemens Healthineers career site.

To all recruitment agencies: Siemens Healthineers does not accept agency resumes. Please do not forward resumes to our jobs alias, employees, or any other company location. Siemens Healthineers is not responsible for any fees related to unsolicited resumes.


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