Sr Site Activation Manager

Job Responsibilities

• Key Responsibilities
• Lead and manage site activation and start-up activities for global clinical trials, ensuring milestones and timelines are met.
• Oversee regulatory, ethics/IRB, and site activation submissions across multiple countries and regions.
• Serve as the primary point of contact for site start-up activities, partnering with sponsors, sites, vendors, and cross-functional teams.
• Drive issue resolution and proactively identify and mitigate risks that may impact study timelines.
• Provide strategic oversight and guidance on country-specific regulatory requirements and start-up processes.
• Track start-up metrics, study deliverables, and activation performance, ensuring compliance with study objectives.
• Support and mentor junior team members and contribute to process improvement initiatives.
• Ensure compliance with GCP, applicable regulations, and company SOPs.
• Collaborate with Project Management and Clinical Operations teams to support successful study execution.
• Manage multiple studies and priorities in a fast-paced global environment.
• At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.
• Salary Range:
• $79,800.00 - $139,600.00
• The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.
• Get to know Syneos Health
• Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
• No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
• http://www.syneoshealth.com
• Additional Information
• Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.