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Principal Medical Writer - Clinical Focus

Role overview

Qualifications

  • Bachelor’s degree required; science-related field preferred
  • Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting
  • Advanced knowledge of ICH and related regulatory guidelines
  • Excellent written English and keen attention to detail

Responsibilities

  • Independently plans and prepares a range of regulatory documents and medical communications
  • Organizes, analyzes, interprets, and presents scientific and statistical information
  • Collaborates with cross-functional internal and external document production teams
  • Works under the direction of Medical Writing management

Key facts

Other skills

  • Detail Oriented
  • Social Skills
  • Microsoft Office
  • Communication

About the company

Veristat logo

Veristat

Veristat is the science-first full-service drug and biologic CRO and consultancy that integrates strategic planning, regulatory expertise, and clinical trial execution to rapidly advance the most complex or novel therapies. Atβ€―Veristat, we collaborate with clients to support the rapid delivery of life-changing therapies, helping them make sound decisions amidst uncertainties. Ourβ€―scientific experts design and conduct the global activities required for any clinical,β€―regulatory, or commercialization program comprehensively and efficiently. ​ With our focus on novel drug development and nearly 30 years of experience, ourβ€―versatile approach and bold scientific thinking make the impossible possible. Dependβ€―on our game-changing expertise and reliable execution for fast results and positiveβ€―impact to support your biologics and drugs to treat rare cancers, CNS/Neurological disorders, Endocrine/metabolic disorders, and infectious diseases. We are…Bold. Scientific. Versatile.β€―Veristat.​ - Veristat has recently been made aware that unknown third parties that have no connection to Veristat are generating fake Veristat job postings, interviews, and even fake employment offers via emails, websites, and various social media platforms, seemingly for the purpose of fraudulently obtaining personal information from legitimate job candidates. All legitimate correspondence from Veristat will originate from our applicant tracking system (Jobvite) or an @veristat.com email address. If you have received outreach from someone claiming to be a member of our team please search our official LinkedIn company page (https://www.linkedin.com/company/veristat-llc), where all members of our authorized recruiting team can be identified, or contact us directly at talentacquisition@veristat.com. Be vigilant.

Company details

Company size501 - 1000

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Job description

Job Description:

Overview

The Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with International Council for Harmonisation (ICH) and other regulatory guidelines, and individual company document standards. The Principal Medical Writer works under the direction of Medical Writing management and collaborates with cross-functional internal and external document production teams.

Make an Impact at Veristat!

Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.

  • 105+ approved therapies for marketing applications prepared by Veristat
  • 480+ oncology projects in the past 5 years
  • 350+ rare disease projects delivered in the past 5 years
  • Flexible, inclusive culture β€” 70% remote workforce, 66% women-led teams Learn more about our core values here!

What we offer:

The estimated hiring range for this role is $142K-153K USD plus applicable bonus. This hiring range is specific to the US and will vary for other regions based upon local market data.  Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.

Benefits vary by location and may include:

  • Remote working
  • Flexible time off
  • Paid holidays
  • Medical insurance
  • Tuition reimbursement
  • Retirement plans

What we look for:

  • Bachelor’s degree required; science-related field preferred.
  • Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute toward this minimum requirement, as determined on a case-by-case basis.
  • Advanced knowledge of ICH and related regulatory guidelines.
  • Excellent written English and keen attention to detail.
  • Strong interpersonal and communication skills.
  • Experience with Microsoft Office Suite is essential, including advanced

Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.

Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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