Remote Site Activation & Quality Lead

Parexel; Tallahassee (FL); On-site; USD 90,000 - 125,000; Full time

Job summary

Parexel is seeking a Site Care Partner to act as the liaison for investigative sites throughout the study lifecycle, driving start-up, activation, recruitment, and quality assurance. You will collaborate with CRA teams and Medical Affairs to optimize country strategies, manage issues, and ensure site readiness and patient safety across global trials.

The role emphasizes data-driven risk mitigation, training coordination, and strong communication with stakeholders to maintain site performance and

Qualifications

• 5+ years prior experience as a CRA in a clinical research or pharma organization.
• Oncology monitoring/CRA experience preferred.
• Experience reviewing monitoring reports.
• Experience in start-up activities through site activation.
• Experience in conduct and close-out activities.
• Knowledge of quality and regulatory requirements in applicable countries.
• Bachelor’s degree or RN; English required; local language proficiency preferred.

Responsibilities

• Lead site start-up and activation activities, coordinating site qualification and activation items.
• Provide country/regional input for strategy, feasibility, and protocol design.
• Support site recruitment planning and enrollment delivery with CRA.
• Maintain relationships with site organizations and strategic partners.
• Ensure training and documentation for site activation and FSFV readiness.
• Collaborate with CRA and other stakeholders to resolve site issues and ensure patient safety.

Skills

Communication skills

Interpersonal skills

Travel willingness

Relationship building

Cross-functional collaboration

Adaptability to new technologies

Regulatory knowledge

Client/stakeholder management

Education

Bachelor’s degree or RN

Job description

Parexel is seeking a Site Care Partner to act as the liaison for investigative sites throughout the study lifecycle, driving start-up, activation, recruitment, and quality assurance. You will collaborate with CRA teams and Medical Affairs to optimize country strategies, manage issues, and ensure site readiness and patient safety across global trials.

The role emphasizes data-driven risk mitigation, training coordination, and strong communication with stakeholders to maintain site performance and