Remote Senior Site Activation Lead

Catalyst Clinical Research, LLC; Tennessee; Hybride; USD 107 000 - 213 000; Plein temps

Avantages offerts par ce poste

None

Résumé du poste

Worldwide Clinical Trials is seeking a Senior Site Activation Manager II to lead start‑up and activation of clinical sites across complex studies. You will collaborate with sponsors, teams, regulators and sites to keep milestones on track and ensure compliant, timely study delivery.

You will mentor colleagues, shape best practices, and contribute to process improvements while managing budgets and timelines across global projects.

Qualifications

• Bachelor’s degree in medical, biological, physical, health, pharmacy or related field; or two-year degree plus four years of experience.
• Minimum seven years of CRO/pharma start‑up, project or site management experience.
• Strong leadership, planning and cross‑functional collaboration across global teams.

Responsabilités

• Lead start‑up and site activation activities across studies.
• Own site activation deliverables, timelines and project performance.
• Coordinate cross‑functional teams to meet critical path milestones on time and budget.
• Monitor regulatory submissions, essential documents and contracts.
• Identify risks, mitigate issues and escalate when needed.
• Track activation metrics and report status to sponsors and stakeholders.
• Develop activation plans and ensure budgets reflect study requirements.
• Support proposals, bids and business development related to site activation.
• Mentor and coach other Site Activation Managers and drive process improvements.

Connaissances

Leadership

Project management

Planning

Organizational skills

Decision-making

ICH GCP

FDA/EU regulations

Cross-cultural comms

English proficiency

MS Office

Formation

Life sciences degree

Outils

MS Office

Description du poste

Worldwide Clinical Trials is seeking a Senior Site Activation Manager II to lead start‑up and activation of clinical sites across complex studies. You will collaborate with sponsors, teams, regulators and sites to keep milestones on track and ensure compliant, timely study delivery.

You will mentor colleagues, shape best practices, and contribute to process improvements while managing budgets and timelines across global projects.