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Co-op, Gene Therapy, Rare Disease
Sanofi. Support development and execution of the Clinical Development Plan (CDP) within the Gene Therapy Rare Disease portfolio under CRD/GPH leadership supervision .
Posted 9/21/2026full-timeWaltham • Massachusetts • United StatesEntry Level💰 $27 - $35 per hourWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates foundational knowledge in Clinical Development Plans (CDP), Target Product Profile (TPP) formulation, and clinical study design, with an understanding of gene therapy and rare disease research. Capable of supporting scientific communications and clinical documentation while collaborating with cross-functional teams.
Highest-signal resume keywords
Clinical Study DesignTarget Product Profile (TPP) FormulationProtocol PreparationGene Therapy KnowledgeBiomedical Research Methodology
ATS Keywords
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Hard Skills
Clinical Development Plan (CDP) ExecutionClinical Trial Protocol PreparationProtocol Amendment PreparationScientific CommunicationsClinical DocumentationRegulatory Affairs KnowledgePreclinical Research FundamentalsBasic Manufacturing ProcessesLife Sciences PrinciplesRare Disease Research Understanding
Industry Keywords
Gene TherapyRare DiseaseClinical ResearchBiomedical SciencesPharmacyRegulatory Affairs
About the role
Key responsibilities & impact- Support development and execution of the Clinical Development Plan (CDP) within the Gene Therapy Rare Disease portfolio under CRD/GPH leadership supervision
- Support activities related to clinical study design
- Contribute to development and maintenance of the Target Product Profile (TPP)
- Assist in formulating and implementing the clinical development strategy
- Support preparation of clinical trial protocols and protocol amendments
- Contribute to scientific communications and clinical documentation
- Support interactions with Key Opinion Leaders (KOLs) as required
- Participate in cross-functional team meetings, including Global Project Team (GPT), Clinical, Regulatory, and other relevant functions
Requirements
What you’ll need- Currently pursuing a bachelor’s or master’s degree in Medicine, Biomedical Sciences, Clinical Research, Regulatory Affairs, Pharmacy, or related life sciences fields
- Must be permanently authorized to work in the U.S. and not require sponsorship of an employment visa at the time of application or in the future
- Must be enrolled in an accredited college or university throughout the duration of the co-op/internship
- Must be able to relocate to the office location
- Must be able to work 40 hours per week, Monday to Friday, for the full duration of the co-op/internship
- Target Product Profile (TPP) formulation and maintenance
- Clinical study design
- Protocol and protocol amendment preparation
- Scientific communications and clinical documentation
- Gene therapy knowledge
- Rare disease research understanding
- Preclinical research fundamentals
- Basic understanding of manufacturing processes
- Biomedical research methodology
- Foundational knowledge of regulatory affairs
- Life sciences principles and Clinical Development Plan (CDP) development and execution
Benefits
Comp & perks- Mentoring and guidance from inspirational leaders
- Supportive, collaborative teams
- Apprenticeships, internships, graduate programs, and international experiences
- Access to the latest tools and digital innovation
- Continuous learning opportunities