Medical Writer- PhD in Life Science Field Career Opportunity
Posted 2025-08-15
Remote, USA
Full Time
Immediate Start
About the position
The Medical Writer position at Medpace offers a unique opportunity to engage in the research of drug and medical device development while making a significant impact on the lives of individuals. This role is ideal for those holding a PhD in a life science field who are eager to explore the research domain and contribute to a team dedicated to bringing pharmaceutical products and medical devices to market. As a Medical Writer, you will be responsible for crafting essential regulatory documents, including IND and NDA modules, clinical study reports, protocols, and protocol amendments. Your work will play a crucial role in ensuring that these documents meet the necessary standards for quality and compliance. In this position, you will coordinate quality control reviews of the documents you produce, maintaining meticulous audit trails of any changes made. You will also interact closely with sponsors and other subject matter experts within Medpace, fostering collaboration and ensuring that all documentation aligns with regulatory requirements. This role not only requires strong writing skills but also demands a high level of attention to detail and the ability to manage multiple projects simultaneously. Your contributions will directly support the mission of Medpace to accelerate the global development of safe and effective medical therapeutics, ultimately improving patient outcomes across various therapeutic areas.
Responsibilities
• Write IND modules, NDA modules and other related regulatory documents
,
• Write clinical study reports, protocols, and protocol amendments
,
• Coordinate quality control reviews of those documents and maintain audit trails of changes
,
• Interact closely with the sponsor, and other Medpace subject matter experts
Requirements
• PhD degree in a life science
,
• Strong computer skills
,
• Project management skills
,
• High attention to detail
,
• Strong communication skills (both written and oral)
Nice-to-haves
Benefits
• Hybrid work-from-home options (dependent upon position and level)
,
• Competitive PTO packages, starting at 20+ days
,
• Competitive compensation and benefits package
,
• Flexible work schedule
,
• Company-sponsored employee appreciation events
,
• Employee health and wellness initiatives
,
• Community involvement with local nonprofit organizations
,
• Discounts on local sports games, fitness gyms and attractions
,
• Modern, ecofriendly campus with an on-site fitness center
,
• Structured career paths with opportunities for professional growth
,
• Discounted tuition for UC online programs Apply tot his job
The Medical Writer position at Medpace offers a unique opportunity to engage in the research of drug and medical device development while making a significant impact on the lives of individuals. This role is ideal for those holding a PhD in a life science field who are eager to explore the research domain and contribute to a team dedicated to bringing pharmaceutical products and medical devices to market. As a Medical Writer, you will be responsible for crafting essential regulatory documents, including IND and NDA modules, clinical study reports, protocols, and protocol amendments. Your work will play a crucial role in ensuring that these documents meet the necessary standards for quality and compliance. In this position, you will coordinate quality control reviews of the documents you produce, maintaining meticulous audit trails of any changes made. You will also interact closely with sponsors and other subject matter experts within Medpace, fostering collaboration and ensuring that all documentation aligns with regulatory requirements. This role not only requires strong writing skills but also demands a high level of attention to detail and the ability to manage multiple projects simultaneously. Your contributions will directly support the mission of Medpace to accelerate the global development of safe and effective medical therapeutics, ultimately improving patient outcomes across various therapeutic areas.
Responsibilities
• Write IND modules, NDA modules and other related regulatory documents
,
• Write clinical study reports, protocols, and protocol amendments
,
• Coordinate quality control reviews of those documents and maintain audit trails of changes
,
• Interact closely with the sponsor, and other Medpace subject matter experts
Requirements
• PhD degree in a life science
,
• Strong computer skills
,
• Project management skills
,
• High attention to detail
,
• Strong communication skills (both written and oral)
Nice-to-haves
Benefits
• Hybrid work-from-home options (dependent upon position and level)
,
• Competitive PTO packages, starting at 20+ days
,
• Competitive compensation and benefits package
,
• Flexible work schedule
,
• Company-sponsored employee appreciation events
,
• Employee health and wellness initiatives
,
• Community involvement with local nonprofit organizations
,
• Discounts on local sports games, fitness gyms and attractions
,
• Modern, ecofriendly campus with an on-site fitness center
,
• Structured career paths with opportunities for professional growth
,
• Discounted tuition for UC online programs Apply tot his job