Clinical Affair cer Writing

**Position Summary**: 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...

**Position Summary**: **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...

**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...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

1. Assisting Regulatory Stack preparation. 2. Assisting Medical affair contents management and creation. 3. Assisting teams across departments, in their regulatory compliance adherence. 4. Ability to research articles to relate regulatory and clinical needs to relevant technology(s). **Job Types**: Fresher, Internship Contract length: 6...

**About the job**: **Job Title**:Medical Writer** Company: MS Clinical Research Pvt Ltd Location: Indiranagar, Bangalore Experience: 2-4 years **About MS Clinical**: MS Clinical is a dynamic and innovative company dedicated to advancing medical research and improving patient outcomes. We specialize in conducting clinical trials and providing...

**Responsibilities**: - Develop and deliver training on Clinical Research, Clinical Data Management (CDM), Pharmacovigilance (PV), and Good Clinical Practice (GCP), with additional knowledge of Medical Writing (MW) and Regulatory Affairs (RA) as a plus. - Conduct assessments and provide feedback to improve trainees’ clinical research skills. - Stay...

Long Description 1ØPurpose of Position The position performs in line with the Bureau Veritas Quality Assurance System, including the BV Code of Ethics and the BV Group policyØ Major ResponsibilitiesAssimilate, understand and operate the BV Certification Quality Management System in all activities relevant to the postResponsible for undertaking audit...

Long Description 1ØPurpose of PositionThe position performs in line with the Bureau Veritas Quality Assurance System, including the BV Code of Ethics and the BV Group policyØMajor ResponsibilitiesAssimilate, understand and operate the BV Certification Quality Management System in all activities relevant to the postResponsible for undertaking audit...