Siemens Life Science Jobs

Siemens Life Science Jobs – Clinical Evaluation Writer Post

Siemens Life Science Jobs – Clinical Evaluation Writer Post. 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:

Job Name: Clinical Evaluation Writer

Job ID: 208793

Location: Bengaluru, India

Organization: Siemens Healthineers

Company: Siemens Healthcare Private Limited

Experience Level: Experienced Professional

Job Family: Research & Development

Job Type: Full Time

Position Summary:

We are looking to add a skilled Clinical Writer to our team. The person in this position must have the ability to independently 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 as well as knowledge/direct clinical experience in using the device or device type in a clinical setting. The expected experience is 4 – 6 years with a minimum of 1– 2 years of CER writing experience is essential. A minimum of 1– 2 years of medical writing/reviewing experience is needed. The

experience is expected to be current or current (preferably within the past 2 years), to provide confidence in their experience considering the rapid nature of updates/changes in the regulatory landscape, the device, its functionalities and also the therapy area.

Preferred Education: Masters’ degree in a life science or biomedical engineering discipline favoured, or equivalent regulatory/writing experience

Preferred Experience:

  1. The expected experience is 4– 6 years with minimum 1– 2 years of CER writing and also reviewing experience. Significant experience writing scientific, medical/clinical, and technological content. Also, a plus would be experience with writing CERs that comply with MEDDEV 2.7/ 1.
  2. Knowledge in the therapeutic area– particularly in the field of diagnostic radiology, interventional radiology and also radiation oncology
  3. Familiarity with numerous country specific standards and also guidelines for medical devices to be able to evaluate as well as provide device appropriate clinical evaluation data for registrations.

Duties and Responsibilities:

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

Organization: Siemens Healthineers

Company: Siemens Healthcare Private Limited

Experience Level: Experienced Professional

Apply Online

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