Remote Early Clinical Scientist - Phase I Trials Lead

Parexel; Phoenix (AZ); Remote; USD 110,000 - 165,000; Full time

Job summary

Parexel is seeking an Early Clinical Scientist to lead or support early phase clinical studies, ensuring scientific and clinical execution aligns with protocol objectives. The ECS collaborates with Clinical Director and internal/external teams to deliver quality data.

The role requires extensive experience in Phase 1, CRO management, and regulatory knowledge, with a focus on timely study delivery and risk mitigation in a fast paced environment.

Qualifications

• Bachelor's degree or higher in Life Sciences or related field with relevant experience.
• Experience managing CROs from sponsor side for Phase 1 trials.
• Use of Clinical Trial Management and Trial Master File systems.
• Authoring Protocol Concepts and trial documentation.
• Ability to facilitate a Trial Team with cross functional partners.

Responsibilities

• Coordinate the design, planning and execution of early phase clinical trials in collaboration with the Clinical Director.
• Oversee trials across programs/therapeutic areas and ensure data validity.
• Manage trial and program projects including team activities and documentation.
• Mentor internal/external teams to meet project objectives and timelines.
• Provide real-time oversight to identify and mitigate issues in ongoing trials.
• Lead risk assessment and contingency planning under accelerated timelines.
• Co-author clinical sections of protocols and related documents.

Skills

MS Office

Team leadership

English proficiency

Multi‑project management

Cross‑functional collaboration

Complex operations management

Therapeutic area knowledge

Education

Bachelor's degree + 7+ years

Master's degree + 5+ years

PhD + 1+ year

Job description

Parexel is seeking an Early Clinical Scientist to lead or support early phase clinical studies, ensuring scientific and clinical execution aligns with protocol objectives. The ECS collaborates with Clinical Director and internal/external teams to deliver quality data.

The role requires extensive experience in Phase 1, CRO management, and regulatory knowledge, with a focus on timely study delivery and risk mitigation in a fast paced environment.