HUN CRA II – Multi Sponsor

🔥 26 minutes ago

🇭🇺 Hungary – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.Why this score:

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• Jobs at this company usually fill in 21 days.
• No salary listed.

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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 activities, and close-out visits on-site or remotely • Evaluate site and site staff performance and provide recommendations and action plans • Communicate and escalate serious issues to the project team • Verify informed consent processes, subject/patient confidentiality, safety, clinical data integrity, protocol deviations, and pharmacovigilance issues • Conduct source document review and verify clinical data accuracy and completeness • Resolve queries remotely and on site and guide site staff • Verify electronic data capture compliance • Manage investigational product inventory, reconciliation, storage, dispensing, administration, labeling, import, and return processes • Review Investigator Site Files and reconcile them with Trial Master Files • Document monitoring activities through required letters, reports, logs, and project documents • Support subject/patient recruitment, retention, and awareness strategies • Track observations, status, and action items to resolution • Manage site-level activities and communications to meet project objectives, deliverables, and timelines • Act as liaison with study site personnel and ensure assigned sites and project team members are trained and compliant • Attend investigator, sponsor, monitoring, project, and clinical training meetings • Support audit readiness, audit preparation, and follow-up actions • For Real World Late Phase: support sites throughout the study lifecycle, perform chart abstraction and data collection, collaborate with sponsor affiliates and local staff, train junior staff, identify out-of-scope activities, and suggest potential sites

🎯 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 • Must complete assigned training as required • Must maintain knowledge of applicable regulations, guidance, and company SOPs/processes

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Reasonable accommodations when appropriate

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