Remote Site Activation Leader — Clinical Start-Up Expert

Parexel; Des Moines (IA); Remote; USD 85,000 - 115,000; Full time

Benefits offered by this job

Health, Vision & Dental Insurance

Tuition Reimbursement

401(k) with Company match

Work/Life Balance

Job summary

Parexel is seeking a Site Activation Leader to join our remote team. In this role, you will provide expert planning and oversight for clinical trial programs, ensuring the high-quality initiation of clinical research sites.

You will lead site activation activities and coordinate across multiple studies. The ideal candidate will have strong site activation leadership skills, knowledge of clinical trial regulations, and the ability to effectively communicate with stakeholders.

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.

Responsibilities

• Lead site activation planning and strategy development.
• Develop, coordinate, and execute study critical path plan.
• Monitor and report site activation progress.
• Provide guidance to site activation team members.
• Manage client relationships regarding site activation timelines.

Skills

Site activation leadership

Strategic planning

Cross-functional coordination

Clinical trial regulations

Project management

Communication skills

Education

Bachelor's degree in Life Sciences

Healthcare, Business Administration or related field

Tools

Clinical Trial Management System

Electronic Data Capture

Job description

Parexel is seeking a Site Activation Leader to join our remote team. In this role, you will provide expert planning and oversight for clinical trial programs, ensuring the high-quality initiation of clinical research sites.

You will lead site activation activities and coordinate across multiple studies. The ideal candidate will have strong site activation leadership skills, knowledge of clinical trial regulations, and the ability to effectively communicate with stakeholders.