Principal Scientific Writer

Key Responsibilities:

• Prepares / supports the preparation of highly complex scientific documents to meet highest quality standards.
• Initiates, implements and champions process improvement techniques.
• Manages multiple projects across multiple brands and therapeutic areas.
• Defines and implements customer management strategies and tactics.
• Develops a Center of Excellence (CoE) for identified TA/disease area/deliverable.
• Provides strategic inputs to development and brand plans and assists in policy decision making as TA/disease/deliverable champion.
• Ideates and implements tactics to influence internal and external development environment.
• Complies with and support group s project management tool, standards, policies and initiatives.
• Commitment to Diversity & Inclusion: :

Essential Requirements: :

• Minimum science degree or equivalent, B.Sc./equivalent with 12 years Clinical Research (CR) experience, M.Sc./M.Pharm +10 years of clinical research (CR) experience
• Provides strategic inputs to development and brand plans and assists in policy decision making as TA/disease/deliverable champion.

Desired Requirements:

• Thorough knowledge of Good Clinical practice. Demonstrated ability to establish effective working relationship in a matrix and multicultural environment.
• Demonstrated presentation and diplomacy skills. Strong customer-oriented mindset.