Job Opportunities in India

1.Content Strategy and Execution: Document Preparation, Development and Finalization/Document
Management
Effectively collect and evaluate data, information, and input from multiple sources,
functions, and regions to create a cohesive content strategy for writing projects.
Plan (including organizing/preparing outlines), write (including first-draft authoring), edit,
review, coordinate, and complete the regulatory documents supporting clinical
development/product registration.
Conduct effective document initiation meeting to ensure authoring team alignment and
understanding.
Build scientific-based rationale that support the purpose of more complex and/or strategic
documents.

• Ensure data are presented in a clear, complete, accurate, and concise manner.

Ensure that key data, statements and conclusions are consistent across related
documents, and that statements and conclusions are integrated, accurate, balanced and
supported by appropriate data.
Coordinate expert/scientific reviews, collate reviewer’s comments, adjust content of
document as required based on internal/external input, and prepare final version.

• Ensure and coordinate quality checks for accuracy.

Exhibit flexibility in moving across development and preparation of multiple document
types.

• Influence or negotiate change of timelines and content with other team members.
• Work with internal and external experts to develop and prepare presentations.
• As needed, may build and manage relationships with vendors/alliance partners.

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2.Project and Stakeholder management
Lead the writing process and apply effective project management skills to ensure timely
completion of high-quality regulatory documents.

• Build/communicate credible writing project timelines.
• Anticipate and mitigate risks to delivery.

Work with teams and stakeholders to ensure smooth and timely development of
documents and escalate issues, as appropriate, to ensure document completion.

• Effectively communicate project status to stakeholders.

3.Knowledge and Skills Development
Maintain and enhance therapeutic area knowledge including disease state and
compound(s) for assigned project(s).
Exhibit flexibility in moving across document types, therapeutic areas, and compounds,
depending on project assignment.

• Maintain and enhance knowledge of regulatory guidelines and publication guidelines.

Possess overarching view of compound, therapeutic area, and external environment
(including competitors) with ability to participate effectively in clinical planning, submission
strategy planning, customer regulatory responses, and/or current awareness literature
updates and reviews.
Maintain and enhance the scientific communications skills to align with the audience needs
and with the changes in technology and platforms.
4.Knowledge Sharing
Provide coaching to others by sharing technical information, giving guidance, answering
questions.

• Recognized for technical expertise in specific document development.

Network with others (including other functions and regions) to identify and share best
practices.

• Contribute to process improvements, suggesting opportunities where appropriate.
• Provide database and other tool (e.g., document management systems) expertise.

Minimum Qualification Requirements:

• Bachelor’s degree in a scientific, health, communications, technology health related field.
• Demonstrated experience in technical/ regulatory scientific writing.
• Strong communication and interpersonal skills.

Successful completion of writing exercise (a writing exercise is required as part of the
candidate evaluation process)
Other Information/Additional Preferences:

• Graduate degree with formal research component or in life sciences.

Demonstrated mastery of verbal and written English skills in the medical, scientific or
technical writing fields.
Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge
and experience specific to hiring area (e.g., neuroscience, oncology, cardiovascular,
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immunology or endocrine expertise).

• Experience writing regulatory, clinical trial documents and/or publications
• Experience in clinical development, clinical trial process or regulatory activities.
• Demonstrated project management and time management skills.

Demonstrated high-level end-user computer skills (e.g., word processing, tables and
graphics, spreadsheets, presentation and templates).
Job Type: Full-time
Pay: ₹1,510,439.03 - ₹2,533,343.36 per year
Schedule:

• Rotational shift

Education:

• Higher Secondary(12th Pass) (Preferred)

Experience:

• total work: 1 year (Preferred)
• Customer service: 1 year (Preferred)

Language:

• English (Preferred)
• Hindi (Preferred)

Work Location: In person