Job Description
📋 Description Lead clinical study protocol development translating strategy into executable protocols. Collaborate on trial design, CRF design, data review, and statistical analysis planning. Review, analyze, and interpret study results; ensure data accuracy and reporting. Identify and address study and program issues; literature reviews for next steps. Coordinate with medical monitor on safety and efficacy data and study communications. Support regulatory documents and clinical sections of submissions and reports. 🎯 Requirements Advanced clinical or science degree (e.g., RN, MA, PharmD, NP, PhD). MA + 5 years or PharmD/PhD + 3 years in clinical/pharmaceutical settings. Experience in planning, executing, reporting and publishing clinical studies. Ability to interpret and present clinical data; literature review skills. Fluent English; strong knowledge of drug development from pre-IND to post-registration. Understanding of trial design, statistics, and cross-functional collaboration. 🎁 Benefits Competitive compensation with bonus potential; generous benefits package. Equity and participation in annual target bonus; 401K with employer contributions. Generous stock options; ESPP plan; PTO and holidays; diverse benefits.
