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Cer Writer Jobs in Ohio (NOW HIRING)

Philips Iberica SAU

$90 - $120/hr

Experience in Medical Writing (CER, CSR, PMCF) and/or Scientific Publications is nice to have * Experience in MedTech, Healthcare Research, Real-World data analytics, Epidemiology, or related fields.

Philips International

$90 - $130/hr

Experience in Medical Writing (CER, CSR, PMCF) and/or Scientific Publications is nice to have* Experience in MedTech, Healthcare Research, Real-World data analytics, Epidemiology, or related fields.

TERRACON

Engineering Technician III

Gahanna, OH · On-site

Tabulate, prepare, and submit data and observation in the form of written and digital reports as ... Successful completion of related internal safety cer * Performs testing, observation, and ...

TERRACON

Engineering Technician III

Gahanna, OH · On-site

Tabulate, prepare, and submit data and observation in the form of written and digital reports as ... Successful completion of related internal safety cer About Us Terracon is a 100 percent employee ...

Palmer Trucks

Service Foreman

Cincinnati, OH

Informs service writer of delays in work performance, necessary repair order extensions, and additional service needs. * Ensures high efficiency of productive employees, analyzes reasons for ...

Arclin

Senior Product Development Chemist

Cleveland, OH · On-site

$90 - $130/hr

Excellent verbal and written communication * Ability to coordinate activities both on site and between sites * Strong technical knowledge of: * Formulating and factory scale manufacturing of rubber ...

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$13

$36

$55

How much do cer writer jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for cer writer in Ohio is $36.73, according to ZipRecruiter salary data. Most workers in this role earn between $24.90 and $46.39 per hour, depending on experience, location, and employer.

What is a Cer Writer?

A CER (Clinical Evaluation Report) Writer is responsible for preparing detailed reports that assess the safety and performance of medical devices. They analyze clinical data, regulatory requirements, and scientific literature to ensure compliance with regulations like the EU MDR. CER Writers collaborate with regulatory teams, medical experts, and researchers to compile and present findings in a clear and structured manner. Their work is essential for obtaining and maintaining medical device approvals in global markets.

What are the most common challenges faced by Cer Writers in their daily work?

One of the most common challenges for CER Writers is gathering and interpreting comprehensive clinical data from various sources while ensuring compliance with ever-evolving regulatory requirements. The role often involves collaborating with clinical, regulatory, and product development teams to fill information gaps and clarify technical details. Additionally, managing tight deadlines and adapting to changes in regulatory expectations can create pressure. However, strong organization and communication skills can help CER Writers overcome these challenges and deliver accurate, timely reports that are critical for medical device approval and market access.

What are the key skills and qualifications needed to thrive in the Cer Writer position, and why are they important?

To thrive as a CER Writer, you need a strong background in scientific writing, clinical research, and regulatory compliance, often supported by a degree in life sciences or pharmacy. Familiarity with relevant guidelines such as MEDDEV 2.7/1 and proficiency with literature databases and referencing tools like EndNote are crucial. Attention to detail, critical thinking, and effective communication are key soft skills for synthesizing data and collaborating with cross-functional teams. These skills ensure the development of high-quality Clinical Evaluation Reports that meet stringent regulatory standards and support product approvals.

What are popular job titles related to Cer Writer jobs in Ohio?

For Cer Writer jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Cer Writer jobs in Ohio look for?

The top searched job categories for Cer Writer jobs in Ohio are:

What cities in Ohio are hiring for Cer Writer jobs?

Cities in Ohio with the most Cer Writer job openings:

Cer Writer jobs near you
Infographic showing various Cer Writer job openings in Ohio as of August 2026, with employment types broken down into 65% Full Time, 33% Part Time, and 2% Contract. Highlights an 54% Physical, 3% Hybrid, and 43% Remote job distribution, with an average salary of $76,401 per year, or $36.7 per hour.

Clinical Development Scientist

Philips Iberica SAU

On-site

$90 - $120/hr

Other

Posted 4 days ago

Job description

Job Title

Clinical Development Scientist

Job DescriptionJob Responsibilities
  • Owns and drives end‑to‑end clinical evidence strategy, defining and linking clinical need, value, TPP, claims, endpoints, and evidence to regulatory acceptance and post‑market requirements with full lifecycle traceability (AD -> PDLM -> PMS).
  • Leads clinical development in cross‑functional AD and PDLM core teams and drives program governance and cross‑project integration enabling global alignment.
  • Owns clinical study design, protocol development, and execution—driving end‑to‑end delivery (kick‑off to results) with optimal data strategy, data integrity, audit readiness, and proactive risk and timeline management.
  • Leads site/KOL engagement and all site‑facing activities (protocol communication, contracts, training) in collaboration with Clinical Science/CPM to ensure compliant execution, protocol adherence, and consistent understanding of product and data requirements.
  • Owns end‑to‑end data strategy and oversees data management in collaboration with data/engineering teams, ensuring data quality, completeness, annotation integrity, adherence to protocol and traceability, while resolving complex data challenges.
  • Collaborates with data/engineering teams on data infrastructure (catalogues, systems) for structured access, traceability.
  • Operationalizes real‑world data by identifying, integrating, and governing data relevance, reliability and scientific validity of diverse data sources, and leads CER and PMCF analytics to generate and continuously assess clinical evidence on safety, performance, and benefit–risk for patient safety and in accordance with regulations and guidance documents.
  • Defines claims validation strategies and leads continuous post‑market evidence surveillance (PMCF/PMS), translating insights into updated claims, regulatory submissions, and expansion of clinical value, indications, and market positioning.
  • Authors and oversees core clinical and regulatory documents (study protocols, CDMA, data strategies, CSRs, CERs, PMCF), ensuring compliant, evidence‑based, and traceable outputs, including integration into IFU and regulatory submissions (e.g., 510k, Technical Documentation, NMPA etc).
  • Drives program risk management and knowledge sharing to optimize execution and evidence generation, and bridges regional and global teams.
  • Communicates insights and aligns stakeholders, builds KOL partnerships, and supports informed decision‑making.
  • Drives scientific dissemination by translating clinical and real‑world evidence into publications, presentations, and competitive insights.
  • Drives structured project management via ADO/Azure, aligning cross‑functional tasks, tracking dependencies, and ensuring clear ownership, prioritization, and timely execution.
Qualifications
  • Medical degree (physician) / Doctor of Medicine, or Medical Technical degree, or a Life Science degree, or a Quantitative Science degree (e.g., Medicine, Technical Medicine, Biomedical Engineering, Biotechnology, Epidemiology, Health Informatics, Data Science).
  • Residency & Advanced Training in Diagnostic Radiology/Ultrasound domain
  • Experience with ultrasound imaging.
  • Experience with developing AI-features in Radiology/Ultrasound.
  • Experience with developing AI‑based medical devices.
  • Experience in Clinical Development / Clinical Research.
  • Experience in clinical evidence communication, research and analysis.
  • Experience in Medical Writing (CER, CSR, PMCF) and/or Scientific Publications is nice to have
  • Experience in MedTech, Healthcare Research, Real-World data analytics, Epidemiology, or related fields.
  • Experienced in regulatory compliance, process improvement and project management
  • Experience with data tools (R, Python, Power BI, Tableau, Git) is nice to have
Preferred Skills
  • Regulatory Compliance
  • Clinical Evaluation and PMCF methodologies
  • Clinical Evidence Generation Strategy
  • Medical and Regulatory Writing (CER, CSR, reports)
  • Data Analysis and Interpretation
  • Quantitative and Real‑World Evidence Methods
  • Project and Program Management
  • Strategic Planning and Business Acumen
  • KPI and Performance Management
  • Document Review and Audit Readiness
  • Continuous Improvement
  • Medical Terminology
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