Guide and support research staff on GCP/ICH compliance and study protocols.
Partner with coordinators and assistants to plan and execute activities.
Anticipate issues and implement corrective actions.
Oversee study tools, metrics, and deliverables.
Manage meeting minutes, communications, and Sponsor/CRO interactions.
Requirements
Extensive Study Coordinator experience
Strong knowledge of ICH/GCP and clinical research regulations.
Skilled in applying SOPs and global guidelines.
Highly organized, able to multitask, and thrive independently or in a team.
Clear, professional communicator with a proactive mindset.
Why join us?
Be part of a forward-thinking team advancing patient-centered research through Decentralized Clinical Trials and, through your leadership, have a direct impact on trial success and patient outcomes.
Apply today and help shape the future of clinical research!
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All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
Benefits
Health insuranceRemote work optionsEquity / stock options
Additional Information
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.
We're looking for a Site Team Lead to support our Decentralized Clinical Trial operations on a new client partnership. You will drive excellence in site activities across Europe through the management of study coordinators, client communication and general project management.
This is a fully remote position offered on a full time, permanent basis, and travel is not required.
This role can be based in the UK, Netherlands, Germany, Sweden, Ireland and a number of locations across Central Eastern Europe.