Remote Project Specialist, Clinical Research Operations

Premier Research Group; Argentina; Remote; ARS 64,187,000 - 91,695,000; Full time

Job summary

Premier Research seeks a Project Specialist to join our Business Operations team. You will coordinate cross-functional project delivery for biotech, medtech, and pharma initiatives, manage communications, and support budget and documentation workflows.

The role requires an associate or bachelor degree in life sciences or related field, 2 years clinical research experience (or 1 year with a Bachelor’s), and knowledge of ICH/GCP, FDA/EU directives, ISO14155, plus MS Office proficiency.

Qualifications

• Associate’s degree (or equivalent) in life sciences or related field; 2 years clinical research experience.
• Bachelor’s degree with 1+ year professional experience in clinical research, healthcare, business, finance, or project management.
• Basic knowledge of ICH/GCP regulations.
• Understanding of FDA/EU directives/ISO14155 and monitoring procedures.
• Proficient in MS Office and project management terminology.

Responsibilities

• Coordinate and oversee project delivery with the Project Manager and cross-functional teams.
• Facilitate team communications, schedule meetings, and maintain agendas/minutes/logs.
• Manage budgets, vendor invoices, change orders, and track services.
• Ensure audit readiness and maintain project systems and study lists.
• Create and distribute study newsletters and maintain distribution lists.

Skills

Clinical research

Microsoft Office

Project management basics

Education

Associate's degree in life sciences/related field

Bachelor's degree in life sciences/related field

Tools

MS Office Suite

Job description

Premier Research seeks a Project Specialist to join our Business Operations team. You will coordinate cross-functional project delivery for biotech, medtech, and pharma initiatives, manage communications, and support budget and documentation workflows.

The role requires an associate or bachelor degree in life sciences or related field, 2 years clinical research experience (or 1 year with a Bachelor’s), and knowledge of ICH/GCP, FDA/EU directives, ISO14155, plus MS Office proficiency.