Executive Director / Senior Director, Clinical Science

Executive Director / Senior Director, Clinical ScienceDirect Hire Full-Time RolePay Rate: $120 - $136 per hourLocation: Redwood City, CA - Remote RoleJob Summary:We are looking for an experienced Clinical Science leader to support and drive our Phase II rare disease program. This person will lead study strategy, oversee trial execution, review data, and work across teams to help advance the program.Duties and Responsibilities:Lead Clinical Science activities for a global Phase II study.Provide scientific oversight from study startup through final readout.Review and help develop protocols, amendments, and study documents.Partner with Clinical Operations to support study execution and timelines.Review safety, efficacy, PK/PD, and biomarker data.Identify risks, trends, and key decisions from study data.Work closely with Biostatistics, Regulatory, Data Management, Safety, and Medical Writing.Support regulatory submissions and health authority responses.Manage CRO and external partner interactions as needed.Present updates and recommendations to leadership.Requirements and Qualifications:degree preferred: PhD, PharmD, MD, or related field.Strong experience in clinical development or Clinical Science.Phase II study experience required.Rare disease experience preferred.Small biotech experience preferred.Strong understanding of GCP and global clinical trials.Excellent communication and leadership skills.Able to work in a fast-paced, hands-on environment. Bayside Solutions, Inc. may collect your personal information during the position application process. Please reference Bayside Solutions, Inc.'s CCPA Privacy Policy at www.baysidesolutions.com.Desired Skills and ExperienceClinical Science, Clinical Development, Phase II Clinical Trials, Rare Disease, Global Clinical Trials, Study Strategy, Scientific Oversight, Trial Execution, Study Startup, Final Readout, Protocol Development, Protocol Amendments, Clinical Study Documents, Clinical Operations, Study Timelines, Safety Data Review, Efficacy Data Review, PK/PD, Biomarker Data, Data Review, Risk Identification, Trend Analysis, Clinical Decision Making, Biostatistics Collaboration, Regulatory Collaboration, Data Management Collaboration, Drug Safety, Medical Writing, Regulatory Submissions, Health Authority Responses, CRO Management, External Partner Management, Leadership Presentations, GCP, Small Biotech, Cross-Functional Leadership, Communication, Fast-Paced Environment