Senior Manager, Site Engagement, Sponsor Dedicated
ICON
Multiple Locations, , US
Clinical site management and oversight
Ich gcp and regulatory compliance
Site-level study start-up and conduct
The role involves establishing and managing site relationships to support global clinical development projects and promote company clinical trials
Job Summary
The role involves establishing and managing site relationships to support global clinical development projects and promote company clinical trials.
The Senior Manager will oversee site-level study activities including start-up, conduct, and close-out, ensuring compliance with regulatory requirements and timelines.
This position requires up to 50% domestic and international travel and collaboration with internal teams and external vendors to achieve recruitment targets and optimize site performance.
Matching Summary
The role involves establishing and managing site relationships to support global clinical development projects and promote company clinical trials.
Skills & Requirements
Must-have
clinical site management and oversight
ICH GCP and regulatory compliance
site-level study start-up and conduct
vendor and trial team collaboration
travel up to 50% domestically and internationally
clinical operations in CRO, pharma or biotech
Nice-to-have
oncology, neurology or immunology therapeutic area experience
strong communication skills in English and native language
critical thinking and medical terminology knowledge
experience with CTMS and eTMF systems
ability to work independently and manage competing priorities
negotiation skills with vendors and sites
Key Requirements
8+ years clinical operations experience
graduate degree in Medical or Life Sciences
experience in site management and clinical study conduct