AI-enhanced for better readability
Clinical Trial Design Specialist – Cardiovascular
Hourly contract: $190-$220/hr
Source: reddit-r-remotejs
Responsibilities
- Lead the design, protocol development, and statistical framework for Phase I–III cardiovascular and inflammatory disease trials.
- Collaborate with clinicians, regulatory experts, and biostatisticians to optimize trial endpoints, patient selection, and study power.
- Ensure compliance with FDA, EMA, and ICH guidelines for trial design and execution.
- Review and incorporate real-world evidence, biomarkers, and emerging trial methodologies into study planning.
- Support cross-functional teams in regulatory submissions, trial monitoring, and results interpretation.
- Provide expertise in risk mitigation, adaptive trial design, and innovative methodologies.
Requirements
- Advanced degree (MD, PhD, PharmD, or MSc) in Clinical Research, Medicine, or Life Sciences.
- 5+ years of experience in clinical trial design and development, with cardiovascular disease experience strongly preferred.
- Proven experience in protocol writing, endpoint selection, and regulatory interactions.
- Familiarity with biostatistics, trial modeling, and adaptive design methodologies.
- Strong understanding of drug development across small molecules, biologics, and novel therapeutics.
- Excellent collaboration, writing, and communication skills for multidisciplinary teams.
Why Join
- Shape the future of cardiovascular and inflammatory disease drug development.
- Work alongside leading clinicians, scientists, and biotech innovators.
- Influence the design of high-impact trials advancing next-generation therapies.
- Flexible engagement opportunities (consulting or full-time) with global exposure.
We consider all qualified applicants without regard to legally protected characteristics and provide reasonable accommodations upon request.