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Premium Employer

Sandoz

Compare

4.0

based on 413 Reviews

387 Sandoz Jobs

Principal Scientific Writer

Sandoz

4.0

based on 413 Reviews

12-16 years

Hyderabad / Secunderabad

1 vacancy

Principal Scientific Writer

Sandoz

posted 4mon ago

Job Role Insights

Flexible timing

Key skills for the job

Clinical Research Medical Writing Project Management Customer Management Clinical Trials Regulatory Compliance

+ 2 more

Job Description

Summary

Working in partnership with the Client Engagement team, Medical Communications, and the Writing delivery team for a designated client group/therapeutic area (TA)/brand, this role will be responsible for delivering and supporting scientific excellence of Medical Communications services across their accounts

About the Role:
Working in partnership with the Client Engagement team, Medical Communications, and the Writing delivery team for a designated client group/therapeutic area (TA)/brand, this role will be responsible for delivering and supporting scientific excellence of Medical Communications services across their accounts

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: :

We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

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.

Skills Desired

Clinical Research, Clinical Trials, Detail-Oriented, Medical Writing, People Management, Project Management, Regulatory Compliance, Safety

Employment Type: Full Time, Permanent

Read full job description

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