Site Activation Manager II

Syneos Health • Morrisville, NC

1d • $79,800 - $139,600

About The Position

Syneos Health is a fully integrated life sciences services organization that partners with innovators across drug development and commercialization. The Clinical Solutions team applies drug-development experience and expertise to understand customer needs and shape solutions. This position focuses on managing site activation activities in the United States and at least one additional global region, including site start-up processes, regulatory and ethics/IRB submissions, and study start-up management. The role requires coordinating multiple deliverables and timelines while working with global, cross-functional stakeholders.

Syneos Health describes its workplace as supportive of career development and progression, with engaged line management, technical and therapeutic area training, peer recognition, and a total rewards program. The company also emphasizes an inclusive culture and a quality-of-life balance. Tasks and responsibilities may be supplemented at the company's discretion; equivalent experience, skills, or education may be considered.

Requirements

• Bachelor’s degree required.
• Minimum of 2 years of experience as a Site Activation Manager (SAM) within the clinical research industry.
• Experience managing site activation activities in the United States and at least one additional global region.
• Strong Site Start-Up (SSU) experience, including regulatory submissions, ethics/IRB submissions, site activation, and study start-up management.
• Proven ability to manage multiple site activation deliverables and timelines simultaneously.
• Strong understanding of GCP, clinical trial regulations, and country-specific start-up requirements.
• Excellent communication, organizational, and stakeholder management skills.
• Ability to work effectively in a global, cross-functional environment.

Responsibilities

• Manage site activation activities in the United States and at least one additional global region.
• Manage site start-up activities, including regulatory submissions, ethics/IRB submissions, site activation, and study start-up management.
• Manage multiple site activation deliverables and timelines simultaneously.
• Work effectively with stakeholders in a global, cross-functional environment.

Benefits

• Company car or car allowance may be included.
• Medical, dental, and vision health benefits.
• Company-match 401(k).
• Eligibility to participate in an Employee Stock Purchase Plan.
• Eligibility to earn commissions or a bonus based on company and individual performance.
• Flexible paid time off (PTO) and sick time, subject to applicable eligibility requirements.
• Career development and progression.
• Technical and therapeutic area training.
• Peer recognition and a total rewards program.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level