Remote US Growth & Lead Gen Specialist

Uptalent.Io; Quilmes; A distancia; ARS 92.724.000 - 139.086.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Site Activation Specialist, ICF Lead to perform country-level SA activities in LATAM with a focus on regulatory compliance and timely study start-up. The role is a senior individual contributor position, operating under moderate supervision, providing local and regional expertise and improving processes across sites.

The candidate will act as SPOC for studies, ensure regulatory and contractual milestones are met, and collaborate with SAMs, PM teams, and sites to drive

Formación

• Bachelor’s degree in Life Sciences or related field required.
• At least 3 years of clinical research or equivalent experience.
• Knowledge of country-specific regulatory requirements in LATAM.
• Ability to manage multiple priorities, meet deadlines and work cross-functionally.
• Strong communication and problem-solving mindset.

Responsabilidades

• Act as the Single Point of Contact (SPOC) for assigned studies with investigators, SAMs, PM teams and internal stakeholders.
• Ensure compliance with local regulations, SOPs, WIs and project timelines.
• Perform feasibility assessments, site identification, study start-up and site activation activities per regional requirements.
• Prepare, review and distribute site documentation for completeness and timeliness.
• Maintain accurate data in internal systems, databases and tracking tools.

Conocimientos

SPOC

Regulatory knowledge

Cross-functional collaboration

Multitasking

Communication skills

Educación

Bachelor's degree in Life Sciences or related field

Descripción del empleo

IQVIA is seeking a Site Activation Specialist, ICF Lead to perform country-level SA activities in LATAM with a focus on regulatory compliance and timely study start-up. The role is a senior individual contributor position, operating under moderate supervision, providing local and regional expertise and improving processes across sites.

The candidate will act as SPOC for studies, ensure regulatory and contractual milestones are met, and collaborate with SAMs, PM teams, and sites to drive