Remote Site Activation Leader | Clinical Start-Up Expert

Parexel; Lincoln (NE); Remote; USD 80,000 - 110,000; Full time

Benefits offered by this job

Health Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

401(k) with Company match

Flexible Spending Accounts

Job summary

Parexel is seeking a Site Activation Leader to work remotely and lead site activation activities for clinical trials. The role includes overseeing operational excellence and ensuring high-quality site initiation across multiple studies.

The ideal candidate will have 4-7 years of relevant experience in clinical research operations, with strengths in strategic planning and cross-functional coordination.

Qualifications

• 4-7 years of experience in clinical research operations with site activation leadership.
• Proven experience leading site activation teams and processes.
• Comprehensive knowledge of clinical trial start-up processes and requirements.
• Strong background in regulatory compliance in clinical research.

Responsibilities

• Lead site activation planning and strategy development for assigned clinical studies.
• Monitor and report site activation progress across multiple studies.
• Provide guidance to site activation team members.
• Manage client relationships and communications regarding site activation timelines.

Skills

Site activation leadership

Strategic planning

Cross-functional coordination

Clinical trial regulations

Project management

Problem-solving

Communication skills

Attention to detail

Education

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

Tools

Clinical Trial Management System

Electronic Data Capture

Interactive Response Technology

Trial Master File systems

Job description

Parexel is seeking a Site Activation Leader to work remotely and lead site activation activities for clinical trials. The role includes overseeing operational excellence and ensuring high-quality site initiation across multiple studies.

The ideal candidate will have 4-7 years of relevant experience in clinical research operations, with strengths in strategic planning and cross-functional coordination.