Co-op, Clinical Research
About The Position
Blueprint Medicines, a Sanofi company, is a global biopharmaceutical company that invents life-changing medicines. We seek to improve and extend patients' lives by solving important medical problems, with a focus on allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a track record of success with two approved medicines, including AYVAKIT/AYVAKYT (avapritinib) which we are bringing to patients with SM in the U.S. and Europe. Leveraging our established research, development, and commercial capability and infrastructure, we aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases and solid tumors. The objective of this Co-op is to gain hands-on exposure to Clinical Development by actively supporting the planning and execution of clinical studies, including study design, feasibility assessments, and data collection processes. The Co-op will participate in projects that build foundational knowledge of clinical data and trial development methodologies, while collaborating with cross-functional teams to understand the interdisciplinary nature of clinical research. Through these experiences, the student will develop a working understanding of clinical trial execution from operational, scientific, technical, and logistical perspectives, and will contribute to ongoing clinical projects at various stages of development by supporting clinical scientists in their day-to-day activities. Projects will be crafted along one or multiple of the following key areas based on interest and business needs:
Requirements
- Actively pursuing a PharmD degree.
Nice To Haves
- Commitment to our Core Values: Patients First, Thoughtfulness, Urgency, Trust, Optimism
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.
- Assist in the planning and coordination of investigator meetings and advisory boards, including logistics and content preparation.
- Support the development of presentation materials and publications for scientific congresses, highlighting key clinical trial findings.
- Perform other duties as assigned.
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What This Job Offers
Career Level
Intern
Education Level
Ph.D. or professional degree
Number of Employees
1,001-5,000 employees
