Manager, Content Strategy and Development (Medical Writing)- Oncology

Scorpion Therapeutics; California (MO); On-site; USD 110,000 - 170,000; Full time

Job summary

Scorpion Therapeutics is seeking a Medical Writer (Manager level, Oncology) to prepare clinical/regulatory documents for global submissions, including study reports, protocols, and investigator brochures.

You will author and review regulatory documents, collaborate with Regulatory Affairs, Clinical Research, Safety, and Data Science, and contribute to submission strategy and document standards across global programs. Experience in oncology and clinical development is essential.

Qualifications

• 6+ years of relevant experience with BS/BA.
• 4+ years with advanced degrees (MA/MPH/MPA/MBA).
• 2+ years with PharmD/PhD.
• Proficiency in regulatory document requirements.
• Microsoft Office proficiency.
• Experience with document management systems.

Responsibilities

• Authoring and reviewing documents per regulatory standards.
• Collaborating with cross-functional teams (Regulatory Affairs, Clinical Research, Safety, Data Science).
• Participating in submission strategy.
• Contributing to document standards and processes.

Skills

Regulatory documents

Microsoft Office

Document management systems

Education

BS/BA

MA/MPH/MPA/MBA

PharmD/PhD

Job description

Role

Medical Writer (Manager level, Oncology) responsible for preparing clinical/regulatory documents for global submissions, including clinical study reports, protocols, and investigator brochures.

Responsibilities

• authoring and reviewing documents per regulatory standards
• collaborating with cross-functional teams (Regulatory Affairs, Clinical Research, Safety, Data Science)
• participating in submission strategy
• contributing to document standards and processes

Requirements

• 6+ years of relevant experience with BS/BA
• 4+ with advanced degrees (MA/MAS/MPH/MBA)
• or 2+ with PharmD/PhD
• proficiency in regulatory document requirements
• Microsoft Office
• document management systems

High-Value

• oncology
• clinical development
• regulatory documentation
• clinical research environment
• experience with global regulatory submissions

Work Setup

not specified; focus on collaboration across multiple teams for global regulatory activities.