Syneos Health 채용 정보 대한민국.

Clinical research associates (CRAs) oversee and ensure the integrity of clinical research studies by monitoring data and processes from a centralized location. They conduct remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. ...

Provides management support and direct supervision to Project Management staff. Responsible for supporting the creation and implementation of individualized development plans, successful performance, employee motivation and retention of PM staff. · ...

Roles within the Clinical Trial Management job family are responsible for all aspects of the development, coordination, and implementation of Phase 1 clinical research studies at the organization's facilities. · Responsible for site management oversight, clinical monitoring and c ...

Manages negotiation of clinical study agreements (CTAs) on a study level and drives CTA document finalization and execution, including contractual language & terms, financial attachments, and investigator grant budgets in collaboration with a global team of site contract negotiat ...

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. · Take the initiative and challenge t ...

Sr. CRA based in Korea · Performs site qualification, site initiation, interim monitoring, site management and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. · Verifies the pro ...

Provides management support and direct supervision to Project Management staff. Responsible for supporting the creation and implementation of individualized development plans, successful performance, employee motivation and retention of PM staff. · ...

CTM II - Sr. responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. · ...

Sr. CRA based in Korea. Performs site qualification, site initiation, interim monitoring, site management and close-out visits ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. · Performs site qualification, site initiation, int ...

Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. · Responsible for site management oversight, clinical monitoring and central monitoring delive ...