Urgent Requirement For Medical Affairs Manager

The Best Enterprises

Manages Study Operational Plan and Cro Activities, Including Project Timelines & Quality of Deliverables Throughout the Life of the Assigned Clinical Trial(s)

reviews and Refines Clinical Operational Plans Including the Study Monitoring At Cro Site for all Be Studies

maintains Frequent and Meaningful Contact with Cros to Assess Performance and Provide Guidance as Needed.

oversees Clinical Trial Sites Adherence to Pertinent Regulations Through Review of Monitoring Reports, Cqa-gcp Audit Report, Communications with Investigators, Study Site Personnel, Cras, and other Cro/designee Personnel

work Closely with other Teams in the Organization, . Quality, Regulatory, Etc

new Product Identification:

suggestion of New Product Ideas for Domestic Markets as Well as International Markets

evaluation of In-licensing Opportunities, Participate in Due-diligence from Medical Perspective.

evaluating New and Unique Drug Formulations with Novel Drug Delivery System

to Represent Company At Dcgi Office for New Drug / Fixed Dose Combination Approvals.

to Effectively Assist in all Regulatory Activities Including Dcgi Dossier Preparation, Ctd Review.

• Experience

  3 - 10 Years

• No. of Openings

  04

• Education

  Professional Degree, Any Bachelor Degree

• Role

  Medical Affairs Manager

• Industry Type

  Hospitals / Medical / Healthcare Equipments

• Gender

  [ Male / Female ]

• Job Country

  India

• Type of Job

  Full Time

• Work Location Type

  Work from Office