Principal Medical Writier

Overview

We are seeking an experienced Principal Medical Writer to lead the development of high-quality clinical and regulatory documents supporting global regulatory submissions. This role plays a critical part in ensuring that documents such as Investigators Brochures (IBs) Clinical Study Reports (CSRs) and Module II summaries that are scientifically accurate consistent and aligned with program objectives and global regulatory requirements.

The successful candidate will act as a lead writer for key summary documents providing strategic guidance to cross-functional teams while overseeing medical writing activities across multiple compounds. This position reports to the Director of Medical Writing (or above).

Key Responsibilities

• Lead the development of high-quality clinical and regulatory documents (e.g. Investigators Brochures Clinical Study Reports clinical summaries and marketing authorization submissions) in compliance with global regulatory guidelines (ICH FDA EMA) and internal standards

• Serve as the lead writer for key summary documents overseeing medical writing activities across multiple compounds or programs

• Provide strategic guidance to cross-functional teams on document content messaging and regulatory positioning to ensure alignment with program goals

• Manage medical writing projects including planning timelines resource coordination and delivery to ensure milestones and submission deadlines are met

• Collaborate with cross-functional stakeholders (Clinical Regulatory Affairs Biostatistics Safety etc.) to gather interpret and accurately present clinical data

• Mentor and support other medical writers ensuring high-quality scientifically sound and consistent deliverables across projects

• Review and edit project-related documents to ensure accuracy clarity consistency and compliance with templates and style guides

• Attend project and team meetings to provide expert input on document development study data interpretation and process improvements

• Contribute to and lead process improvement initiatives to enhance efficiency quality and consistency in document preparation

• Develop maintain and refine standard operating procedures (SOPs) templates and best practices for medical writing

• Stay current with evolving global regulatory requirements industry trends and therapeutic area knowledge to ensure compliance and innovation

Qualifications

• Bachelors degree in a scientific clinical regulatory or related field required; advanced degree (e.g. MSc PhD PharmD MD) preferred

• Minimum of 7 years of experience in medical writing within the biopharmaceutical biotechnology or CRO industry; equivalent experience in clinical or preclinical development will also be considered

• Strong knowledge of global regulatory requirements and guidelines (e.g. ICH FDA EMA) across all phases of clinical development

• Broad understanding of clinical research processes including study design data analysis and regulatory submission requirements

• Demonstrated ability to lead writing activities for complex documents and provide strategic input to cross-functional teams

• Excellent written and verbal communication skills with the ability to clearly and accurately present complex scientific and clinical information

• Strong organizational time management and project management skills with the ability to manage multiple priorities and meet tight deadlines

• Proven ability to work collaboratively in a cross-functional team-oriented environment while also operating independently when needed

• High attention to detail with a commitment to quality consistency and scientific accuracy

• Proficiency in Microsoft Word and document formatting best practices

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or any other status protected by applicable law. is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.