Job Title:
Senior Site Contracts Specialist
Location:
USA – NC (Remote)
Job ID:
25101737
Company Overview:
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We bring clinical, medical affairs, and commercial insights together to deliver outcomes addressing modern market realities.
Our Clinical Development model places the customer and the patient at the center of everything we do. Whether in a Functional Service Provider (FSP) partnership or a Full-Service environment, employees collaborate to innovate and accelerate therapy delivery, improving lives globally.
Work Here Matters Everywhere – over 29,000 employees in 110 countries.
Why Syneos Health:
Career development and progression opportunities
Supportive line management and technical/therapeutic area training
Peer recognition and total rewards programs
Inclusive Total Self culture promoting authenticity and belonging
Job Summary:
The Senior Site Contracts Specialist manages and executes site identification processes for clinical trials, ensuring compliance with regulations, SOPs, and project requirements. This role includes negotiating site contracts, maintaining performance metrics, and serving as the primary point of contact for investigative sites.
Key Responsibilities:
Manage and execute site identification process according to regulations, SOPs, and project requirements
Complete and negotiate site confidentiality agreements (CDAs) and site information forms (SIFs) with investigative sites
Maintain, review, and report on site performance metrics; identify improvement areas and implement corrective actions
Serve as primary contact for sites, providing guidance throughout the site identification process
Track site identification progress and ensure proper documentation
Contribute to the design, implementation, or delivery of processes, programs, and policies
Mentor and provide guidance to junior staff or manage defined project components
Collaborate with cross-functional teams to ensure seamless execution
Ensure compliance with relevant regulations, SOPs, and project requirements
Qualifications:
Bachelor’s degree in a related field or equivalent experience
Practical knowledge in clinical research or site management
Strong understanding of regulations, SOPs, and site identification requirements
Excellent negotiation, communication, and interpersonal skills
Experience managing CDAs and SIFs
Strong organizational, time management, and analytical skills
Proficiency with relevant site management software and tools
Ability to work independently and collaboratively
Preferred Certifications:
Relevant certifications in clinical research or site management
Salary Range:
$56,400 – $95,900 (based on qualifications and experience)
Benefits:
Health benefits (Medical, Dental, Vision)
401(k) with company match
Employee Stock Purchase Plan eligibility
Flexible Paid Time Off (PTO) and sick leave
Potential for company car or car allowance
Bonus/commission eligibility
Impact and Contribution:
Ensures efficient and effective site identification processes to support clinical trial success
Contributes to project execution by applying practical knowledge and experience
Supports junior team members and drives process improvements
Job Category:
Site Start-Up / Clinical Operations / Clinical Trial Support
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