What are the responsibilities and job description for the Pharma Regulatory Submissions _ Coauthoring Consultant position at Cygnus Professionals Inc.?
Project duration: Long term contract
Working model: Hybrid working from Philadelphia
Client: A Big Pharma
Role Description: R&D coauthoring consultant with demonstrated experience and mastering of Pharma process for regulatory submissions across R&D - research, development, safety, regulatory, and medical. Ideal candidate would have prior consulting experience with planning, authoring, reviewing and approving regulatory documents including creation, version control, approval, and real-time co-authoring of all submission-related documents. Very Strong Pharma background is compulsory.
Note : Most Importantly, the proposed candidate need to have seasoned experience on CSR submission Module 2 and Module 5. Also, should be a more seasoned and consultative profile.
