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Senior Clinical affairs analyst

ID de Puesto
479585
Publicado desde
17-Oct-2025
Organización
Siemens Healthineers
Ámbito de trabajo
Quality Management
Empresa
Siemens Healthcare Private Limited
Nivel de experiencia
Profesional Experimentado
Tipo de jornada
Jornada completa
Modalidad de trabajo
Oficina/Solo presencial
Tipo de contrato
Indefinido
Ubicación(es)
  • Bangalore - Karnataka - India
We are looking to add an experienced Clinical Writer to our team. The person in this position must be able to independently contribute 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 knowledge/direct clinical experience in the use of the device or device type in a clinical setting. The experience is expected to be current or recent (preferably within the past two years), to provide confidence in their experience considering the rapid nature of updates/changes in the regulatory landscape, the device, its functionalities and the therapy area.

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

Preferred Experience: 
1. The expected experience is 3-4 years with minimum 1 – 2 years of CER writing and reviewing experience. Significant experience writing scientific, medical/clinical, and technical content.
2. Knowledge in the therapeutic area – specifically in the field of diagnostic radiology, interventional radiology and radiation oncology
3. Familiarity with various country specific standards and regulations for medical devices to be able to assess and provide device appropriate clinical evaluation data for registrations.

Duties and Responsibilities

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