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Key Responsibilities:
- Lead clinical trial execution across the site network, overseeing study start-up, activation, and ongoing operational performance.
- Assess protocol feasibility and support study planning, including resource allocation, budget considerations, and recruitment strategy development.
- Drive study start-up timelines, coordinating with internal teams to ensure efficient site activation.
Qualifications:
- Bachelor’s degree in a scientific, healthcare, or related field.3+ years of clinical research experience.
- Experience working with a clinical research network, CRO, or pharmaceutical/biotech sponsor strongly preferred.
- Strong knowledge of ICH-GCP guidelines and regulatory requirements governing clinical trials.
Additional Information:
- This remote role requires up to 30% travel
- At Hawthorne Health, we are committed to transforming how clinical research is delivered by bringing high-quality trials closer to the communities that need them most.
- Our team is passionate about improving patient access, accelerating study timelines, and partnering with sponsors to advance meaningful medical innovation.
Hawthorne Health
Hawthorne Health is a leading community site network and home research visit solution provider, with 20+ sites and more than 2,000 research experienced healthcare professionals across the U.S. They leverage convenient, trusted, healthcare locations, identified patient data, and intelligent technology to accelerate patient access, improve retention, and reduce study costs.