Clinical Site Activation & Relationship Lead

Parexel

Raleigh (NC)

On-site

USD 85,000 - 110,000

Full time

14 days+
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Job summary

Parexel is seeking a Site Care Partner to liaise with investigative sites throughout study lifecycles, handling start-up, activation, recruitment, and quality assurance. You will coordinate with CRA teams, ensure site readiness, and manage issues to protect patient safety while maintaining Parexel standards.

Responsibilities include site qualification, activation planning, monitoring readiness, and collaboration with regulatory authorities to ensure timely site activation and compliant study

Qualifications

  • Knowledge of GCP/ICH guidelines and regulatory requirements.
  • Strong communication and interpersonal skills.
  • Ability to travel as needed to sites and regions.
  • Experience building relationships with investigators and sites.
  • Ability to manage cross-functional relationships and escalations.

Responsibilities

  • Lead site start-up/activation and manage relationships with sites and vendors.
  • Coordinate site qualification, ICF finalization, SIV, and activation tasks.
  • Support site recruitment planning and enrollment delivery with CRA collaboration.
  • Provide local country input for feasibility and SOC practices.
  • Monitor site performance, resolve issues, and ensure patient safety.
  • Ensure Parexel standards, training, timesheets, and expense reporting.

Skills

GCP Knowledge
Communication skills
Interpersonal skills
Travel willingness
Cross-functional collaboration
Relationship building
Data analysis

Education

Bachelor's degree or RN

Job description

Parexel is seeking a Site Care Partner to liaise with investigative sites throughout study lifecycles, handling start-up, activation, recruitment, and quality assurance. You will coordinate with CRA teams, ensure site readiness, and manage issues to protect patient safety while maintaining Parexel standards.

Responsibilities include site qualification, activation planning, monitoring readiness, and collaboration with regulatory authorities to ensure timely site activation and compliant study

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