Remote Early Clinical Scientist | Phase I Oversight

Parexel; Cheyenne (WY); Remote; USD 110,000 - 180,000; Full time

Job summary

Parexel is seeking an Early Clinical Scientist to coordinate the design, planning and execution of early phase trials in collaboration with the Clinical Director. You will oversee risk management, safety assessments, and data integrity across programs and therapeutic areas.

You will co-author clinical documents, support trial operations, and lead cross-functional teams to ensure compliant trial conduct and timely deliverables in a remote or flexible setting.

Qualifications

• Experience in managing CROs from the Sponsor side for Ph1 clinical trials.
• Use of Clinical Trial Management and Trial Master File systems.
• Authoring Protocol Concepts.
• Facilitating a Trial Team with cross functional partners such as regulatory, data managers, statisticians, etc.

Responsibilities

• Coordinate design, planning and execution of early phase trials with Clinical Director and teams.
• Oversee trial safety assessment and risk management to ensure data validity.

Skills

CRO management

CTMS familiarity

Protocol concepts

Cross-functional leadership

Microsoft Teams

GCP knowledge

Medical writing

Education

Life Sciences degree

Bachelor’s degree

Master’s degree

PhD

Tools

Trial Master File systems

Microsoft Teams

Job description

Parexel is seeking an Early Clinical Scientist to coordinate the design, planning and execution of early phase trials in collaboration with the Clinical Director. You will oversee risk management, safety assessments, and data integrity across programs and therapeutic areas.

You will co-author clinical documents, support trial operations, and lead cross-functional teams to ensure compliant trial conduct and timely deliverables in a remote or flexible setting.