Site Start-Up Specialist II — Activation & Compliance

Syneos Health; Ciudad de México; Presencial; MXN 320.000 - 520.000; Jornada completa

Descripción de la vacante

Syneos Health is seeking a Site Activation Specialist II in Mexico City to lead country-level site start-up activities, manage local submissions, and coordinate with CSA/SAM. The role requires strong clinical trial knowledge, vendor management, and excellent communication.

You will ensure timely submissions, maintain TMF, and support process improvements in a dynamic, global clinical solutions team. The position emphasizes cross-functional collaboration across regulatory, sites, and sponsors,

Formación

• Bachelor's degree in a related field (clinical trials preferred).
• Knowledge of clinical trial processes across phases II–IV and ICH GCP.
• Ability to manage site start-up tasks and external vendors.
• Strong written and verbal communication and interpersonal skills.
• Ability to manage multiple project budgets with increasing complexity.
• Quality-driven in all managed activities.
• Good negotiating skills and problem-solving abilities.
• Demonstrated ability to work independently as well as part of a team.

Responsabilidades

• Ensure quality deliverables at the country level with oversight from the SSU Country Manager.
• Monitor basic financial aspects and hours/tasks per contract, escalate discrepancies.
• Review SOPs/WIs and keep training records updated; ensure timesheet compliance.
• Support continuous improvement of SSU components at the country level.
• Submit documents to TMF per SOP/Sponsor requirements.
• Coordinate local submissions, EC/RA applications and regulatory authority interfaces.
• Oversee site activation end-to-end at country/site level.

Conocimientos

Clinical trial knowledge

Start-up process

Vendor management

Organizational skills

Communication skills

Budget management

Quality-driven

Negotiation

Problem-solving

Independent worker

Educación

Bachelor's Degree

Descripción del empleo

Syneos Health is seeking a Site Activation Specialist II in Mexico City to lead country-level site start-up activities, manage local submissions, and coordinate with CSA/SAM. The role requires strong clinical trial knowledge, vendor management, and excellent communication.

You will ensure timely submissions, maintain TMF, and support process improvements in a dynamic, global clinical solutions team. The position emphasizes cross-functional collaboration across regulatory, sites, and sponsors,