Remote Site Activation Leader | Study Start-Up Expert

Parexel; Salem (OR); Remote; USD 110,000 - 165,000; Full time

Benefits offered by this job

Health Insurance

Vision Insurance

Dental Insurance

Tuition Reimbursement

Vacation & Holidays

Flexible Spending Account

Health Savings Account

Work/Life Balance

401(k) Match

Pet Insurance

Job summary

Parexel in the United States (remote) is seeking a Site Activation Leader to provide planning and oversight for clinical trial site start-up activities, from feasibility to activation, across multiple studies.

You will lead cross-functional teams, ensure regulatory compliance, manage timelines, support proposals, and drive quality improvements in site activation processes within a collaborative Clinical Operations environment.

Qualifications

• 4–7 years of clinical research operations experience with site activation leadership
• Strong knowledge of clinical trial start-up processes and regulatory requirements
• Excellent written and verbal communication with senior stakeholders and investigators

Responsibilities

• Lead site activation planning and strategy for assigned studies from feasibility to activation
• Coordinate study critical path, site selection, regulatory submissions, and ethics processes
• Monitor activation progress, identify delays, and drive cross-functional issue resolution
• Provide guidance to activation teams and liaise with project management and operations
• Manage client communications on timelines and deliverables for designated accounts
• Support proposals and bid pursuits with activation expertise
• Standardize activation processes and drive quality initiatives

Skills

Site Activation Leadership

Strategic Planning

Cross-Functional Coordination

Regulatory Compliance

Project Management

Education

Bachelor's degree in Life Sciences, Healthcare, Business Administration, or a related field

Job description

Parexel in the United States (remote) is seeking a Site Activation Leader to provide planning and oversight for clinical trial site start-up activities, from feasibility to activation, across multiple studies.

You will lead cross-functional teams, ensure regulatory compliance, manage timelines, support proposals, and drive quality improvements in site activation processes within a collaborative Clinical Operations environment.