3.0 - 7.0 years

0 Lacs

chennai, tamil nadu

On-site

Role Overview: As a Medical Writer at RRD GO Creative, you will be responsible for developing high-quality and scientifically accurate medical and regulatory documents, including clinical study reports, protocols, and brochures. Your role involves creating clear and concise medical content tailored for healthcare professionals, regulatory agencies, and internal stakeholders. Conducting thorough research and literature reviews to ensure content accuracy and compliance with industry standards is essential. Collaboration with subject matter experts, scientists, and regulatory teams is crucial to develop compelling and compliant medical writing materials. You will also need to adhere to client a...

Posted 1 month ago

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Research Analyst-II ( Regulatory Affairs) Makro Group

2.0 - 4.0 years

2 - 4 Lacs

hyderabad

Work from Office

Research Analyst - II Roles & Responsibilities: To perform Secondary research in order to provide the detailed information or the complete profile of the product. Thorough understanding of regulations, Ability to grasp new concepts quickly and to assimilate and evaluate scientific data keeping up to date with changes in regulatory legislation and guidelines Strong secondary research skills and Sound Knowledge on drug labels and clinical trial Knowledge on drugs, devices and other products regulations Able to evaluate applicable laws and regulations to determine impact & Able to mentor team members Compile and analyze data using modern and traditional methods to collect it. Responsible for co...

Posted 2 months ago

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Research Analyst-II ( Regulatory Affairs) Makro Group

2.0 - 4.0 years

2 - 4 Lacs

Hyderabad

Work from Office

Posted 4 months ago

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