Global Site Activation Leader

Socket.dev; North Carolina; Hybrid; USD 107,000 - 213,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Site Activation Manager to lead start-up activities in the assigned therapeutic area, coordinating site identification, contracts, and regulatory tasks for NA. The role reports to a senior Site Activation leader within the therapeutic area.

The successful candidate will drive timelines, manage cross-functional teams, and ensure timely, compliant activation. Requires seven years of CRO/pharma startup/site management experience and proven leadership

Qualifications

• Four-year college curriculum or equivalent with a major concentration in medical, biological, physical, health, pharmacy or other related science, or two-year college degree plus four years experience within clinical research.
• Seven years relevant CRO/pharmaceutical industry experience, preferably in Start-up Management, Project Management, and/or Site Management experience.

Responsibilities

• Serve as the primary point of communication for study start-up and maintenance activities on assigned projects.
• Oversee project activities of cross-functional groups involved in site activation to ensure critical path activities are completed on time and within budget.
• Ensure accurate compilation, management, tracking and analysis of site activation activities.
• May support feasibility and/or site identification activities, as needed.
• Work closely with team members to expedite Site Qualification and Selection process.
• Communicate Site Activation & Regulatory project status to Sponsor, GPL/CPM and project team.

Skills

Leadership

Organization

English proficiency

Cross-cultural communication

Stakeholder management

Problem solving

Team motivation

Adaptability

Education

Four-year college degree or equivalent in life sciences

Bachelor’s degree in medical/biological/health science

Job description

Worldwide Clinical Trials is seeking a Senior Site Activation Manager to lead start-up activities in the assigned therapeutic area, coordinating site identification, contracts, and regulatory tasks for NA. The role reports to a senior Site Activation leader within the therapeutic area.

The successful candidate will drive timelines, manage cross-functional teams, and ensure timely, compliant activation. Requires seven years of CRO/pharma startup/site management experience and proven leadership