Blueprint Medicines, a Sanofi company, is seeking to improve and extend patients' lives by solving important medical problems, with a focus on allergy/inflammation and oncology/hematology. This Co-op role aims to support the planning and execution of clinical studies to advance their pipeline of programs.
Requirements
- Actively pursuing a PharmD degree.
Responsibilities
- Assist Medical Directors and Clinical Scientists in gathering and organizing scientific and medical information to support study protocols and development plans.
- Support the drafting and review of clinical study documents such as protocols, Investigator Brochures, Informed Consent Forms, and training materials.
- Help analyze clinical data and literature to identify trends, safety signals, and protocol-related issues under supervision.
- Participate in safety and efficacy data reviews and assist in preparing materials for internal review meetings.
- Contribute to the summarization of study results and relevant scientific literature to support clinical insights.
- Collaborate with departments such as Data Management and Translational Research to support data analysis and reporting efforts.
- Support the development of presentation materials and publications for scientific congresses, highlighting key clinical trial findings.
Other
- This is a lab-based position, we expect 5 days on site.
- Commitment to our Core Values: Patients First, Thoughtfulness, Urgency, Trust, Optimism
- Blueprint’s offices are a business casual environment.
- Spring 2026 Co-op Program Dates:Monday, January 5th – Friday, June 26th
- You will be employed by Magnit, LLC for all purposes and not Blueprint Medicines, a Sanofi Company.
