Site Team lead

Jobgether; Remote; GBP 100,000 - 125,000; Full time

Job summary

An opportunity with a recruitment platform seeking a Site Team Lead to manage decentralized clinical trial operations in the United Kingdom. The ideal candidate will oversee research staff, ensure compliance with clinical protocols, and communicate effectively with stakeholders in a remote environment. This role offers a competitive salary in a collaborative team, focusing on improving patient outcomes and supporting decentralized clinical trials across Europe.

Benefits

Competitive salary

Fully remote work

Professional growth opportunities

Collaborative team environment

Supportive work culture

Qualifications

• Extensive experience as a Study Coordinator in clinical research.
• Strong knowledge of ICH/GCP guidelines and regulatory requirements.
• Proficiency in applying SOPs and global clinical research standards.
• Highly organized with the ability to multitask.
• Excellent communication skills.
• Flexibility to operate across multiple European locations.

Responsibilities

• Guide and support research staff on GCP/ICH compliance and study protocols.
• Lead, mentor, and coordinate study coordinators to execute trial activities.
• Monitor study tools, metrics, and deliverables.
• Maintain clear and accurate documentation.
• Serve as the primary point of contact for sponsor interactions.
• Anticipate operational challenges and implement corrective actions.

Job description

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Site Team Lead in United Kingdom.

We are seeking a Site Team Lead to oversee and coordinate decentralized clinical trial operations across Europe. In this role, you will lead and support research staff, manage study coordinators, and ensure adherence to clinical protocols and regulatory standards. You will play a key part in planning, executing, and monitoring trial activities, while maintaining effective communication with stakeholders. This position requires a proactive and organized professional who can manage multiple priorities, anticipate issues, and implement solutions efficiently. The role offers an opportunity to directly impact trial success and improve patient outcomes in a collaborative and innovative environment.

Accountabilities

• Guide and support research staff on GCP/ICH compliance and study protocols.
• Lead, mentor, and coordinate study coordinators and assistants to execute trial activities effectively.
• Monitor study tools, metrics, and deliverables to ensure high-quality results.
• Maintain clear and accurate documentation, including meeting minutes and project communications.
• Serve as the primary point of contact for sponsor and CRO interactions.
• Anticipate operational challenges and implement corrective actions promptly.

Requirements

• Extensive experience as a Study Coordinator in clinical research.
• Strong knowledge of ICH/GCP guidelines and regulatory requirements.
• Proficiency in applying SOPs and global clinical research standards.
• Highly organized with the ability to multitask and work independently or collaboratively.
• Excellent communication skills and a proactive, solution-oriented mindset.
• Flexibility to operate across multiple European locations remotely.

Benefits

• Competitive salary and permanent full-time position.
• Fully remote work with flexible arrangements.
• Opportunity to contribute to patient-centered clinical trials across Europe.
• Supportive, collaborative, and forward-thinking team environment.
• Professional growth and development in decentralized clinical trial operations.

By submitting an application to this posting, the applicant acknowledges that Jobgether will process their personal data as necessary to evaluate their candidacy, provide feedback, and, when appropriate, share relevant information with potential employers. Such processing is carried out on the basis of legitimate interest and pre-contractual measures in accordance with applicable data protection laws. The applicant may exercise their rights of access, rectification, erasure, and objection at any time as provided under the GDPR.