Corbus Culture:

Our passion. Our purpose. At Corbus, it starts at our core. 

We look for unique talent. Our people are brilliant, they break barriers and are not defined by a title. Eclectic experiences make Corbus a special place to share ideas and grow. At Corbus, transformative ideas can come from anyone, anywhere and anytime. We offer our team flexibility and the opportunity to excel in their professional journey. We provide a welcoming space where collaboration, mentorship and diversity are encouraged. We come together, like no other, to elevate each other and focus on what’s best for patients. 

About Corbus

Corbus is a precision oncology company with a diversified portfolio and is committed to helping people defeat serious illness by bringing innovative scientific approaches to well-understood biological pathways. Our pipeline is comprised of two experimental drugs targeting solid tumors: CRB-701, a next-generation antibody drug conjugate (“ADC”) that targets the expression of Nectin-4 on cancer cells to release a cytotoxic payload and CRB-601, an anti-integrin monoclonal antibody that blocks the activation of TGFβ expressed on cancer cells. The pipeline also includes CRB-913, a highly peripherally restricted cannabinoid type-1 (“CB1”) receptor inverse agonist for the treatment of obesity. Corbus is headquartered in Norwood, Massachusetts. For more information on Corbus, visit corbuspharma.com. Connect with us on Twitter, LinkedIn and Facebook.

Corbus Pharmaceuticals Holdings, Inc. is an equal opportunity employer

The Temporary Medical Writer is responsible for various medical writing initiatives.  The person in this role is responsible for ensuring all documents are written in accordance with applicable regulations and completed on time.   

Job responsibilities:

• Provide medical/regulatory writing and editing expertise for study reports and regulatory submission documents and in particular compile and summarize data for briefing book for regulatory meetings, investigator brochures, and IND applications
• Write, review, and edit preclinical pharmacology, pharmacokinetic and toxicology technical documents for organization, clarity, language/grammar, consistency, and scientific standards
• Coordinate, synthesize, and integrate scientific and medical input from internal and external contributors to meet deliverable and publication deadlines for regulatory documents, as well as manuscripts, abstracts, and presentations for scientific meetings and publications.
• Author documents while contributing expertise, knowledge/skills related to clinical drug development, and scientific/technical expertise
• Experience in performing medical-database searches (e.g., Medline, PubMed, etc.).
• Experience as primary author on scientific publications.

Skills & Requirements:

• IND, CTA and IB writing experience required
• Knowledge of FDA and EMEA regulations, GCP and ICH guidelines desirable
• Excellent computer skills with experience using Microsoft Word (Word, Excel, PowerPoint) applications to prepare charts, tables, reports and presentations. Experience with email and calendar programs also required.
• 5+ years medical writing experience. Industry medical writing experience strongly preferred
• Life Sciences degree required.
• Experience with regulatory toxicology studies (in vitro/in vivo) and/or a PhD/MS in Life Sciences is a plus