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Isf Jobs In M - 32 Job Positions Available

1 – 8 of 32 jobs

Overview As a Clinical Research Associate in Real World Late Phase, you monitor and manage trial sites to ensure regulatory compliance and data integrity. You will perform remote and on-site activities across initiation, monitoring, and close-out,

Syneos Health  1 day ago

Overview In this role you support clinical trial sites to ensure regulatory and protocol compliance across a multi-sponsor program. You work with cross-functional teams to monitor data integrity, manage site activities, and drive quality through both

Syneos Health  1 day ago

Overview As a Clinical Research Associate, you oversee site qualification, initiation, monitoring, and close-out to ensure protocol and regulatory compliance across Germany. You work with cross-functional teams to safeguard data integrity, patient safety, and trial quality,

Syneos Health  1 day ago

Overview As a CRA II for our multisponsor team in Germany, you oversee site performance and trial data integrity through monitoring and site management. You align with ICH-GCP, GPP and protocol requirements, liaising with site staff

Syneos Health  1 day ago

Overview As a Clinical Research Associate with Syneos Health in Germany, you will oversee site qualification, initiation, monitoring, and close-out to ensure regulatory and protocol compliance. You’ll assess site performance, support data integrity, and manage communications

Syneos Health  1 day ago

Overview As a CRA for a single sponsor partnership in Germany, you will oversee site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. You will work with cross-functional teams to assess site

Syneos Health  1 day ago
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Overview As a Clinical Research Associate, you will oversee site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. You’ll work with cross-functional teams to protect patient safety and data integrity across trials,

Syneos Health  1 day ago

Overview In this role, you will monitor clinical sites to ensure regulatory and protocol adherence, overseeing data integrity and patient safety. You will collaborate with cross-functional teams across Austria and Germany, applying GCP/ICh guidance and SOPs.

Syneos Health  1 day ago

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Regulatory Requirements

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Ips

German

Archiving

Query Resolution

Informed Consent

Document review

Data Integrity

Electronic Data Capture

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