Clinical Scientist, Director

Bostonfull timeRemote

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senior

$225k–$240k

H1B: no

Celeatherapeutics The Clinical Scientist, Director at Celeatherapeutics supports clinical development strategies and study execution for respiratory disease treatments. The role involves collaboration with internal teams and CRO partners to ensure high-quality clinical data and alignment with development plans.

Responsibilities

Support the development and execution of clinical development strategies and plans.
Contribute to clinical study design and implementation, including development of study concepts, protocols, schedules of assessments, medical monitoring plans and related clinical documents including investigator and site training materials.
Conduct ongoing review and interpretation of clinical safety data and identify emerging trends, issues, and opportunities both in real-time and for aggregate review.
Support clinical data review, including review of listings, tables, and figures.
Partner with Clinical Operations and Data Management to identify and resolve data quality issues.
Contribute to clinical study reports, regulatory documents, presentations, and other clinical development deliverables.
Work closely with CRO clinical teams to support study planning, execution, and delivery.
Review and provide input on CRO deliverables, including study plans, protocols, data review materials, and clinical reports.
Help identify and escalate study issues and work collaboratively with CRO partners to develop solutions.

Qualification

PhDWhy Join Celea TherapeuticsCollaborate with a passionate

Required

PhD, PharmD, MS or advanced scientific degree in a relevant discipline.
8+ years of relevant experience in clinical development, clinical research, or a related pharmaceutical/biotechnology environment.
Experience supporting clinical trials in a biotechnology or pharmaceutical company including reviewing, aggregating and synthesizing blinded safety data and troubleshooting missing data and assessments, and reviewing risk-based monitoring output
Experience working directly with CROs and other external clinical development partners.
Understanding of clinical trial methodology, clinical development processes, and GCP principles.
Strong scientific writing and communication skills.
Excellent organizational and project-management skills.
Entrepreneurial mindset and comfort operating in a fast-paced, early-stage environment.
Proficiency using AI tools to work smarter — curiosity about how technology can improve the quality and speed of your work.

Preferred

Respiratory disease area experience is preferred.
Experience with Phase 1–3 clinical development.
Experience supporting regulatory submissions or interactions.
Experience working with external investigators.
Why Join Celea Therapeutics
Play a pivotal role in advancing life-changing therapies for patients with devastating lung diseases.
Shape the foundation of a Phase 3 biotech poised for significant growth.
Collaborate with a passionate, mission-driven leadership team.