Position Summary:

　　We are looking for a Clinical Expert who is responsible for clinical evaluation and PMCF activities; collaboration with CLM owners/Risk manager/PMS manager.

　　Qualification:

　　· MBBS or equivalent Medical degree; specialization in Radiology is preferred.

　　· Knowledge/direct clinical experience in the use of the device or device type in a clinical setting. The expected experience is 3-4 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.

　　· Knowledge on Medical devices regulations

　　· 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 Experience:

　　Significant experience writing scientific, medical/clinical, and technical content.

　　Knowledge in the therapeutic area – specifically in the field of diagnostic radiology, interventional radiology and radiation oncology

　　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

　　Collaborate with the project/program stakeholders for product knowledge and information to develop quality content for the CER’s and within the required timelines.

　　Able to work in cross functional teams with strong communication, presentation & interpersonal skills

　　Analytical thinking skills with strong demonstration of scientific writing and verbal communication.

　　Manages projects in the context with full responsibility for the results and drives the development of clinical evaluation report, Pre-CER, CLP and/or services that are on time and meets the quality, regulatory and customer requirements .

　　Mentoring and coaching the team on technical topics

　　Responsible to implement process changes as per the new/updated regulatory requirements

　　Defining clinical development activities/ PMCF activities

　　participating in the assessment of clinical benefit-risk profile of the clinically relevant risks identified in the risk management upon request of the risk manager

　　assessing and aligning the device’s clinical benefit-risk profile between the clinical evaluation and risk management jointly with the risk manager

　　supporting post-market surveillance manager on the PSUR/PMS reporting by providing summary of the relevant clinical evaluation report contents, and in planning/coordinating device’s PMS activities with the device’s clinical evaluation and PMCF.