Remote Site Start-Up Specialist II

Syneos Health, Inc.; Mexico; Remote; MXN 420,000 - 620,000; Full time

Job summary

Syneos Health, Inc. is seeking a Site Activation Specialist II in Mexico, with remote work option and cross-functional collaboration. The role focuses on country-level start-up activities, regulatory submissions, and document management to enable site activation.

Candidates should have a life sciences degree and solid clinical trial knowledge, with strong communication and budgeting skills to support timely, compliant start-ups across multiple sites.

Qualifications

• Bachelor’s degree and clinical trial knowledge are required.
• Strong written and verbal communication and interpersonal skills.
• Ability to manage multiple tasks and budgets with high attention to detail.
• Familiarity with regulatory submissions and site activation processes.
• Experience coordinating with vendors and cross-functional teams.

Responsibilities

• Ensure quality deliverables at country level with oversight from SSU Country Manager.
• Monitor timelines and track milestones in SSU systems; explain delays and plan contingencies.
• Review SOPs/WIs and keep training records updated; ensure timesheet compliance.
• Support site start-up components and document collection; submit EC/RA applications.
• Act as liaison between sites and functional leads; oversee end-to-end site activation.
• Provide country-start-up advisor input; maintain regulatory intelligence repository.
• Assist with investigator contracts, budgets, and site contract negotiations.
• Maintain QA focus across country start-up activities and documentation.

Skills

Bachelor’s Degree

Clinical trial knowledge

Documentation skills

Vendor management

Organization

Communication skills

Budget management

Quality-driven

Negotiation

Problem-solving

Teamwork

Education

Bachelor’s Degree in Life Sciences or related field

Job description

Syneos Health, Inc. is seeking a Site Activation Specialist II in Mexico, with remote work option and cross-functional collaboration. The role focuses on country-level start-up activities, regulatory submissions, and document management to enable site activation.

Candidates should have a life sciences degree and solid clinical trial knowledge, with strong communication and budgeting skills to support timely, compliant start-ups across multiple sites.