Medical Writing Job at ClinChoice | Life Sciences Graduates Apply Now
Are you a Life Sciences graduate looking for a high-impact Medical Writing job? ClinChoice careers in Bengaluru offer an exciting opportunity to contribute to Clinical Evaluation Reports (CERs) and Safety Surveillance Reports (SSRs) within the medical device sector. This role blends scientific writing, regulatory compliance, and cross-functional collaboration, making it one of the most sought-after Life Sciences jobs for professionals aiming to accelerate their career in medical and clinical writing.
About the Company:
ClinChoice is a leading partner to global pharmaceutical, medical device, and consumer care innovators. Established in 1995, the company provides expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology. ClinChoice helps partners accelerate clinical trials, enhance patient safety, and ensure global regulatory compliance through data-driven insights and innovative solutions.
Job Overview:
The Medical Writer, Shared Services will support the creation and execution of Clinical Evaluation Reports (CERs) and Safety Surveillance Reports (SSRs) for assigned therapeutic areas within the medical device business. The role involves developing Clinical Evaluation Plans, ensuring regulatory compliance, linking documentation to quality systems, and collaborating with cross-functional teams including Medical Directors, Post Market Surveillance, R&D, and Regulatory Affairs.
Key Responsibilities:
- Writing Clinical Evaluation Plans and Reports (CERs) in compliance with regulatory requirements.
- Preparing Safety Surveillance Reports (SSRs) aligned with local procedures and client guidelines.
- Linking CER and SSR files to Quality Systems and Regulatory documents for consistency.
- Developing communication strategies for CERs/SSRs with cross-functional partners.
- Participating in workshops and initiatives to improve global processes and efficiency.
- Supporting audits and inspections related to CER/SSR processes.
- Collaborating with Medical Directors, Post Market Surveillance, R&D, and Regulatory Affairs teams.
Educational Requirements:
- Graduate or Postgraduate degree in Life Sciences.
- Minimum 3 years of experience in medical, scientific, or technical writing.
Skills Required:
- Strong knowledge of Clinical Evaluation Report (CER) and Safety Surveillance Report (SSR) requirements.
- Experience in the medical device industry, regulatory compliance, and adverse event reporting.
- Familiarity with quality systems, risk management, and biostatistics.
- Excellent scientific and technical writing skills.
- Regulatory/Notified Body audit experience preferred.
Advance your career with ClinChoice careers in Bengaluru and take the next step in Life Sciences jobs focused on Medical Writing. This role offers hands-on experience with global regulatory standards and scientific documentation, providing an opportunity to grow professionally while contributing to patient safety and medical device innovation.
