Senior Specialist, Submission Management Bristol Myers Squibb

3.0 - 5.0 years

0 Lacs

hyderabad, telangana, india

Remote

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a w...

Posted 2 weeks ago

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Lead - Scientific Writing Indegene

10.0 - 14.0 years

0 Lacs

karnataka

On-site

As a Medical Writer, you should have MBBS/PhD/MDS/BDS/MPharm/PharmD education qualification with 10 to 12 years of experience in writing Clinical & Regulatory documents supporting global filings (CTD Module 2 and Module 5). Your role will involve handling complex Medical Writing projects, providing review support for medical writing deliverables, training junior writers, and authoring a broad set of different clinical document types that support regulatory filings. Demonstrating excellence in focused/lean writing, leading cross-functional teams, understanding the clinical development process, and possessing effective communication, time management, organizational, and interpersonal skills ar...

Posted 1 month ago

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Lead - Scientific Writing Indegene

10.0 - 14.0 years

0 Lacs

karnataka

On-site

Role Overview: You will be responsible for handling complex Medical Writing projects, providing review support for medical writing deliverables, training junior writers, and authoring a broad set of different clinical document types that support regulatory filings. Your role will also involve leading cross-functional teams, understanding the clinical development process, and possessing effective communication, time management, organizational, and interpersonal skills. Key Responsibilities: - Prepare and review clinical study reports, protocols, investigator brochures, submission documents, and other regulatory documents on investigational drugs in various stages of clinical development. - Ap...

Posted 3 months ago

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