Senior or Principal Regulatory Medical Writer

Senior or Principal Regulatory Medical Writer

Would you like to join one of the fastest-growing organizations with a stated goal of using latest and

greatest AI, GenAI, LLM, Cloud and Digital Technologies to advance drug development and improve

patient care pathways. WriteMed.AI helps Biopharma and Life Sciences Companies, among others, to

reduce the time for writing medical publications and regulatory documents. Our Medical Writing Team

support our customers’ missions with creative and transformative spirit of innovation across all

therapeutic areas.

Role Overview

This is an opportunity to be a Principal or Senior Medical Writer, to guide our AI Architects, Data

Scientists and Engineers towards medical writer needs, evaluate and improve the quality of outputs, and

be the voice of the customers internally.

Required Qualifications

• This position will be a remote position, with occasional ( approximately 10-20%) travel to client

sites and conferences

years of work experience in academia or industry with at least 5+ years of medical writing work

experience in the industry

experience in the industry

Reports, Protocols, Investigator Brochures, Informed Consent Forms, 510Ks, NDAs

Preferred Qualifications

more executive team members

difficult challenges

Responsibilities

interpretation and summary, as well as adherence to AMA manual of style. Provide statistical

summary of document quality

of medical writers across the globe

document quality, accuracy, and style

reimbursement to expense reimbursement programs that can be used for needs that best suit

you and your family, from student loan repayment, to childcare, to pet insurance

every voice and support you in doing the best work of your career

depending on skills, experience, job-related knowledge and location

compensation

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