$115,500 to $135,000 annually; discretionary bonus...
Remote
Prepare high-quality regulatory documents
Clinical study reports
Study protocols
ImmunityBio, Inc. is seeking a Senior Medical Writer to prepare high-quality regulatory documents related to cancer therapies and immunotherapies. The ideal candidate should possess significant experience in medical writing, particularly with regulatory submissions, and have a strong scientific background in oncology or immunotherapy
Job Summary
The Senior Medical Writer will be responsible for the preparation of high-quality regulatory documents, including clinical study reports, clinical summaries and overviews, study protocols, Investigator’s brochures, and informed consent forms.
The Senior Medical Writer may also be responsible for planning, managing, and preparing internal and external communications of key scientific and clinical data, including abstracts, poster and oral presentations, manuscripts, congress materials, and educational/training materials.
ImmunityBio offers a competitive total rewards benefits package, including medical, dental, vision, 401(k) with company match, and unlimited PTO for exempt employees.
Matching Summary
Match Score: 85
ImmunityBio, Inc. is seeking a Senior Medical Writer to prepare high-quality regulatory documents related to cancer therapies and immunotherapies. The ideal candidate should possess significant experience in medical writing, particularly with regulatory submissions, and have a strong scientific background in oncology or immunotherapy.
Salary
$115,500 to $135,000 annually; Discretionary bonus and equity award; Medical, Dental, Vision, 401(k) match, Unlimited PTO (Exempt)
Skills & Requirements
Must-have
prepare high-quality regulatory documents
clinical study reports
study protocols
Investigator's brochures
informed consent forms
scientific and clinical data
oncology, immunotherapy, or related field
Nice-to-have
harness and amplify the immune system
transform the lives of patients
collaborative team environment
professional development opportunities
Key Requirements
Bachelor's degree in science-related fields with 4+ years of experience
Master's degree in science-related fields with 2+ years of experience
Experience in NDA submissions
Writing CSRs, IBs, clinical study protocols
Proficient knowledge of AMA writing guidelines
Extensive knowledge of FDA, EMA, and ICH guidelines