Site Team Lead (Clinical Research)

TL;DR

Site Team Lead (Clinical Research): Driving excellence in site activities for decentralized clinical trials through management of study coordinators and client communication with an accent on GCP/ICH compliance and project oversight. Focus on implementing corrective actions, overseeing study metrics, and ensuring seamless Sponsor/CRO interactions.

Location: Remote; must be based in the UK, Netherlands, Germany, Sweden, Ireland, or Central Eastern Europe. Hybrid work is encouraged for those living near company offices.

Company

hirify.global provides end-to-end consulting solutions in regulatory sciences, clinical research, and pharmacovigilance to biotech, med device, and pharmaceutical organizations.

What you will do

• Guide and support research staff on GCP/ICH compliance and study protocols.
• Partner with coordinators and assistants to plan and execute site activities.
• Anticipate potential issues and implement effective corrective actions.
• Oversee study tools, performance metrics, and project deliverables.
• Manage meeting minutes and handle interactions with Sponsors and CROs.

Requirements

• Extensive experience as a Study Coordinator.
• Strong knowledge of ICH/GCP and clinical research regulations.
• Proven skill in applying SOPs and global guidelines.
• Ability to multitask and work independently or within a team.
• Professional communication skills and a proactive mindset.

Culture & Benefits

• Remote-first work environment with flexibility for hybrid collaboration.
• Commitment to diversity, equity, and inclusion.
• Supportive culture encouraging innovation and entrepreneurial spirit.
• Human-centric hiring process with personal reviews and no AI screening tools.