Intern, Clinical Operations Associate
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.
Requirements
- Currently pursuing a degree in Life Sciences, Biotechnology, Clinical Research or a related field
- Strong analytical and problem-solving skills, with the ability to develop and improve tools and processes
- Strong written and verbal communication and interpersonal skills with the ability to collaborate effectively with cross-functional teams
- Detail-oriented with strong organizational skills and the ability to manage multiple tasks and priorities
- Ability to quickly prioritize large lists of tasks and execute them in a timely manner
Nice To Haves
- Commitment to our Core Values: Patients First, Thoughtfulness, Urgency, Trust, Optimism
- Exposure to medical and scientific terminology
- Ability to learn rapidly on the job
- Advanced knowledge of Word, Excel, and PowerPoint
- Knowledge of how to utilize AI to work more efficiently
- Previous experience in a clinical research setting or related field
Responsibilities
- Help study teams in the day-to-day supervision of clinical trial execution, with a focus on site start up, patient enrollment, and data flow metrics from the clinical sites and vendors
- Support complex clinical trial activities in support of the Clinical Study Managers and other team members
- Ensure tracking of essential documents are received and filed, review site documents for accuracy, provide clinical team support with document filing and management
- Ensure tracking of patient status throughout the study at investigative sites
- Track and monitor sample collection, central laboratory reporting, and manage laboratory testing schedule
- Review data generated from clinical sites and assist with analysis and reporting of findings
- Coordinate the activities from third party vendors including metrics, accruals, process planning, and implementation
- Determine ways to streamline processes within the study teams and with cross functional collaboration, preferably utilizing Artificial Intelligence (AI) to work more efficiently
- Assist with financial tracking within the study budgets
- Collaborate with the ClinOps Outsourcing & Site Budgets team to evaluate company needs for potential vendors, assist with setting up demonstrations and capabilities meetings, coordinate collection of internal feedback on services and/or performance, and develop financial tools and/or training materials for the Clinical Operations team.
- Assist with integration efforts as needed.
- Perform other duties as assigned.
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What This Job Offers
Career Level
Intern
