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IQVIA Inc. is seeking a Lead Medical Writer with a strong background in clinical writing to manage advanced projects related to clinical study reports and protocols. The ideal candidate will possess relevant educational qualifications and a minimum of three years of experience in medical writing, particularly with an emphasis on collaboration and communication.
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Job Summary
Acts as Lead Medical Writer on more advanced writing projects, preparing assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines.
Manages day-to-day workload, identifies project needs, tracks timelines, implements customer requests, and keeps management abreast of progress and potential problems.
Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or technical writing.
Matching Summary
Match Score: 75
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IQVIA Inc. is seeking a Lead Medical Writer with a strong background in clinical writing to manage advanced projects related to clinical study reports and protocols. The ideal candidate will possess relevant educational qualifications and a minimum of three years of experience in medical writing, particularly with an emphasis on collaboration and communication.
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Skills & Requirements
Must-have
Lead medical writing projects
Prepare clinical study reports
Adhere to SOPs and timelines
Communicate with customers
Understand drug development regulations
Nice-to-have
Provide feedback to peers
Deliver basic training
Propose SOP revisions
Key Requirements
3 years of prior relevant experience
Familiarity with clinical study reports and protocols
Ability to identify deficiencies in documents
Good understanding of statistical methods
In-depth knowledge of drug development and regulations