Position Summary: The Senior Medical Writer/Principal Medical Writer will be responsible for leading the development of high-quality and on-time clinical study documents.

Responsibilities

include clinical document planning, writing, editing/formatting, and performing QC review.

Requirements

. The successful candidate has a clear understanding of content

for key clinical documents based on regulatory

for all phases of development and will complete MW activities with impeccable attention to detail.

based on regulatory guidances Ensures smooth and effective document management from start to finish (ie, from template to final, approved version) in collaboration with Sponsor, external vendors, and/or internal Precision project teams/departments Ability to independently formulate key messages from clinical study data Ability to author complex content using knowledge/skills and understanding of processes Ability to communicate clearly and concisely both in writing and verbally with internal and client teams Contributes to the development and maintenance of medical writing processes, SOPs, templates, and work instructions for key documents Excellent problem-solving skills Performing literature-based research to support writing activities Other duties as assigned

for all phases of development Impeccable attention to detail and ability to complete writing assignments in a timely manner Ability to work effectively in a fast-paced environment with multiple high priority projects with no instruction on routine work and minimal instruction on new assignments Preferred: Advanced degree (MS/PhD) Oncology and/or rare disease experience (especially protocol and CSR development) Precision is required by law in some states or cities to include a reasonable estimate of the

Qualifications

: Minimum Required: BS degree or equivalent in a scientific or medical discipline with relevant writing expertise 5+ years of experience as a medical writer in the sponsor and/or CRO setting or 7+ years of experience as a Principal Medical Writer.

Requirements (Ie, EudraCT, CT.Gov)

, and eCTD

Compensation

range for this role.

range takes into account the wide range of factors that are considered in making

decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled.

decisions are dependent on the facts and circumstances of each case.

Benefits

, life insurance and disability

, parental leave, and paid time off for sick leave and vacation, among other

Reasonable estimate of the current range $100,600 — $182,600 USD Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice . Precision Medicine Group is an Equal Opportunity Employer.