Site Activation & Relationship Lead

Regulatory Jobs; North Carolina; On-site; USD 70,000 - 110,000; Full time

Job summary

Parexel is hiring a Site Care Partner in the United States to liaison with investigative sites through a study lifecycle, focusing on site start‑up, activation, recruitment and quality assurance.

The role requires coordinating with CRA, managing site relationships, ensuring patient safety, and aligning with Parexel processes and regulatory standards.

English proficiency expected, travel as needed; Bachelor’s degree or RN required.

Qualifications

• Knowledge of GCP/ICH guidelines and regulatory requirements.
• Strong computer skills and ability to learn new technologies.
• Excellent communication and interpersonal skills.
• Willingness to travel as required.
• Experience coordinating with cross-functional teams.
• Ability to interact with internal and external stakeholders.

Responsibilities

• Oversee site start-up and activation activities to enable study initiation.
• Support country-specific site qualification and activation processes.
• Collaborate with CRA to ensure site readiness for FSFV.
• Maintain relationships with Site Organizations and partners.
• Manage communications and resolve escalated site issues.

Skills

Good Clinical Practice

Strong communication

Interpersonal skills

Travel willingness

Stakeholder management

Cross-functional collaboration

Regulatory understanding

Education

Bachelor’s degree or RN in a related field

Job description

Parexel is hiring a Site Care Partner in the United States to liaison with investigative sites through a study lifecycle, focusing on site start‑up, activation, recruitment and quality assurance.

The role requires coordinating with CRA, managing site relationships, ensuring patient safety, and aligning with Parexel processes and regulatory standards.

English proficiency expected, travel as needed; Bachelor’s degree or RN required.