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Key Responsibilities:
- Lead or contribute to feasibility assessments for client requests for proposals.
- Review clinical protocols, study assumptions, and operational plans for US and global trials.
- Synthesize competitive landscape, historical recruitment, and epidemiology evidence into recommendations.
Qualifications:
- Bachelor’s in life sciences with at least two years of clinical trial feasibility or related experience.
- Ability to interpret clinical, scientific, and operational information to develop clear recommendations.
- Professional proficiency in English; postgraduate degree or experience in oncology/rare disease preferred.
Skills & Attributes:
- Strong analytical and critical-thinking skills with attention to detail.
- Ability to manage multiple concurrent deliverables and communicate rationale effectively.
- Advanced proficiency in Microsoft Excel, PowerPoint, and Word; familiarity with clinical-trial intelligence platforms.
Precision for Medicine
Precision for Medicine combines clinical-trial execution, scientific expertise, laboratory capabilities, and advanced data sciences to help life sciences organizations improve the speed, cost, and likelihood of successful clinical development. The organization has a strong focus on oncology and rare diseases, offering the opportunity to contribute to complex programs that bring meaningful therapies to patients.