Principal Med Writer Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. As the lead writer, reviews documents for the team and provides training and guidance to junior team members. Provides advice on document development strategy, regulations and industry best practices. Demonstrates subject matter and therapeutic area expertise. Acts as backup program manager. Collaborates with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence. Researches, writes, and edits clinical study reports and study protocols, and summarizes data from clinical studies. Researches, writes, and edits clinical study reports and study protocols, and summarizes data from clinical studies. - Serves as primary author who writes and provides input on complex clinical and scientific and program level documents, including IBs, INDs, and MAAs. - Provides senior level review of routine and complex documents. Provides training and mentorship for other writers and program managers on document preparation, the use of software for document development, document types, regulatory requirements, and therapeutic area knowledge. - Ensures compliance with quality processes and requirements for assigned documents. As the subject matter expert, develops and reviews best practices, methods and techniques for achieving optimal results, including various client-specific processes, and leads process improvement initiatives. May also develop, review and manage performance metrics for assigned projects. - May serve as backup program manager. Identifies and resolves out-of-scope activities. Duties could include developing timelines, budgets, forecasts and contract modifications, and assisting business development with client presentations and proposal text review and attending bid defense meetings and capabilities presentations. - Represents the department at project launch meetings, review meetings, and project team meetings. Experience Level Senior Level
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- It is a Full Time Nurse / Compounder job for candidates with 5 - 6+ years Experience.
More about this Principal Medical Writer job
Who is eligible to apply for this Principal Medical Writer job at Thermo Fisher Scientific India Private Limited?
Ans : Candidates should have All Education levels for this Principal Medical Writer job offered by Thermo Fisher Scientific India Private Limited.
How much can you earn in this position?
Ans : Salary details will be shared during the hiring process.
What shift and timings does this job follow?
Ans : This Principal Medical Writer job follows a Day shift.
Do you need to visit the office for this job?
Ans : Yes, candidates need to visit the office and work from the location in Ambernath, Mumbai.
How many openings are available for this position?
Ans : There is 1 opening available for this position.
Is this job open for all genders?
Ans : Yes, this Principal Medical Writer job is open for both male and female candidates.
Where is this job located?
Ans : This Principal Medical Writer job is located in Ambernath, Mumbai.
Why should you apply for this Principal Medical Writer job?
Ans : The employer has not disclosed the salary for this role, but it is a Full Time opportunity with 1 opening available.