Clinical Trial Manager I – Sponsor Dedicated

🔥 1 minute ago

🇬🇷 Greece – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Perform site qualification, site initiation, interim monitoring, site management, and close-out visits on-site or remotely • Evaluate site and site staff performance and provide site-specific recommendations • Escalate serious issues and develop action plans with project team guidance • Verify informed consent processes, subject/patient confidentiality, safety, and clinical data integrity • Assess site processes under Clinical Monitoring/Site Management Plans • Conduct source document review and verify clinical data in case report forms • Resolve queries remotely and on site within agreed timelines • Use hardware and software for clinical project data review and capture • Verify electronic data capture compliance • Manage investigational product inventory, reconciliation, storage, dispensing, administration, and related documentation • Review Investigator Site Files and reconcile them with Trial Master Files • Document monitoring activities through letters, trip reports, communication logs, and project documents • Support subject/patient recruitment, retention, and awareness strategies • Track observations, site status, and action items to resolution • Manage site-level activities and communications to meet project objectives, deliverables, and timelines • Liaise with project site personnel, CRAs, and Central Monitoring Associates • Ensure assigned sites and site team members are trained and compliant • Attend investigator, sponsor, global monitoring, and clinical training meetings • Support audit readiness, audit preparation, and follow-up actions • For Real World Late Phase: provide site support throughout the study lifecycle, perform chart abstraction and data collection, and collaborate with sponsor affiliates, medical science liaisons, and local country staff

🎯 Requirements

• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements • Good computer skills and ability to embrace new technologies • Excellent communication, presentation and interpersonal skills • Ability to manage required travel of up to 75% on a regular basis • Ability to perform clinical monitoring and site management activities on-site or remotely • Knowledge of local requirements for real world late phase study designs, where applicable

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Total Self culture • Diversity, inclusion, and belonging initiatives