
Urgent Search) Principal Scientific Writer
4 weeks ago
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.
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