Senior Clinical Scientist, ECD

This is a fully remote position, open to applicants in California.

📋 Description

• Oversee key components of ECD clinical studies or multiple studies simultaneously.

• Lead the design of studies, which encompasses objectives, endpoints, eligibility criteria, and assessment schedules.

• Draft and evaluate protocols, informed consent forms (ICFs), case report forms (CRFs), and other study-related documents.

• Make significant contributions to the clinical development strategy and decisions at the study level.

• Conduct medical and clinical data reviews to guarantee data quality and integrity.

• Examine intricate datasets to uncover trends, risks, and opportunities.

• Manage daily clinical science responsibilities for assigned studies.

• Facilitate the resolution of issues, risks, and operational challenges at the study level.

• Prioritize tasks across studies to maintain quality, timelines, and program effectiveness.

• Spearhead the creation of abstracts, presentations, and manuscripts.

⛳️ Requirements

• Possession of an advanced degree (PhD, PharmD, MD, or equivalent; MS, MPH, RN with relevant experience considered).

• A minimum of 6 years of experience in clinical research, clinical science, or a related field.

• Extensive experience in leading clinical studies and contributing to study design.

• Proven track record in leading and executing clinical studies, encompassing clinical data review, decision-making at the study level, issue management, and cross-functional coordination.

🏝️ Benefits

• Comprehensive medical, dental, vision, life, and disability insurance plans.

• Complimentary testing for employees and their immediate family members.

• Fertility care benefits available.

• Leave for pregnancy and bonding with a newborn.

• 401k retirement benefits.

• Commuter benefits provided.

• Employee referral program in place.