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Siemens Life Science Clinical Evaluation Writer Job Vacancy

Siemens Life Science Clinical Evaluation Writer Job Vacancy. Candidates with life science background and relevant experience and invited to apply online for Clinical Evaluation Writer vacancy. Interested and eligible candidates can check out all of the details on the jobs details, jobs descriptions, eligibility, application procedure and such given below:

Name of the Post: Clinical Evaluation Writer

Job Family: Quality Management

Job ID: 214482

Location: Bengaluru, India

Organization: Research & Development

Company: Siemens Healthcare Private Limited

Experience Level: Experienced Professional

Job Family: Research & Development

Job Type: Full Time

Job Description:

Position Summary:

We are wanting to add an experienced Clinical Writer to our team. The person in this position should be able to individually add to the development of initial and update( s) of CER’s that support the applicable regulatory submission requirements for the medical device products.

An experienced Clinical Analyst professional has relevant medical/life-science

qualification and also knowledge/direct clinical experience in the use of the device or device type in a clinical setting. The expected experience is 4 – 5 years with a minimum of 2 years of CER writing experience is essential.

Preferred Education: Masters’ degree in life science or biomedical engineering discipline is chosen, or equal regulatory/writing experience.

Preferred Experience:

  1. The expected experience is 4– 5 years with minimum 2 years of CER writing as well as reviewing experience. Significant experience writing scientific, medical/clinical, and also technical content. Also, a plus would be experienced with writing CERs that conform to MEDDEV 2.7/ 1.
  2. Knowledge in the therapeutic area– specifically in the field of diagnostic radiology, interventional radiology and also radiation oncology.
  3. Familiarity with various country-specific standards and regulations for medical devices to be able to assess and also provide device appropriate clinical evaluation data for registrations.

Duties and also Responsibilities:

  1. Collaborate with the project/program stakeholders for product knowledge and info to develop quality content for the CER’s and within the required timelines.
  2. Screen and also summarize the literature for relevant clinical data.
  3. Review literature to elucidate the clinical problem as well as current treatment techniques.
  4. Study as well as report device characteristics and also instructions for use.
  5. Assess data for similar competitor devices.
  6. Sum up post-marketing surveillance as well as risk management data for the target device.
  7. Able to work in cross-functional teams with strong communication, presentation & interpersonal skills.
  8. Analytical thinking abilities with a strong demonstration of scientific writing and verbal communication.

Organization: Siemens Healthineers

Company: Siemens Healthcare Private Limited

Experience Level: Experienced Professional

Apply Online

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