Jobs at Syneos Health

Conducts clinical trial site qualification, initiation, monitoring, management, and close-out visits while ensuring protocol, regulatory, and GCP compliance. Reviews source documents, medical records, informed consent, clinical data, investigational product handling, and essential trial files. Supports recruitment, audit readiness, query resolution, site training, documentation, and project timelines. May mentor junior CRAs and support real-world late-phase studies through chart abstraction, regulatory coordination, site identification, and sponsor collaboration.

The CRA II- SCRA conducts site qualification and management activities, ensuring compliance with regulatory guidelines, supporting patient recruitment, and documenting site activities.

The CRA II- SCRA will oversee site activities, ensuring compliance with regulatory standards while performing monitoring, data verification, and site management throughout the study lifecycle.

Conducts site qualification, initiation, monitoring, management, and close-out visits ensuring ICH/GCP and protocol compliance. Reviews source documents, verifies CRF data and IP handling, resolves queries, maintains ISF/TMF reconciliation, documents activities, supports recruitment and audit readiness, and may train junior staff. Performs on-site and remote monitoring and collaborates with sponsors and local staff.

Conduct site qualification, initiation, monitoring (on-site/remote) and close-out visits ensuring ICH/GCP and protocol compliance. Review source documents and CRFs, manage IP accountability, reconcile ISF/TMF, document findings, support recruitment/retention, and assist with audit readiness. Collaborate with sponsors, local staff, and train junior staff when needed. For Real World Late Phase, perform chart abstraction and local site support throughout study lifecycle.

Conduct site qualification, initiation, monitoring, management and close-out (on-site or remote) ensuring ICH-GCP and protocol compliance. Perform source document/CRF review, query resolution, IP inventory/reconciliation, ISF/TMF reconciliation, and regulatory documentation. Support recruitment/retention, audit readiness, training, and project-level site communication. For Real World Late Phase, perform chart abstraction, collaborate with sponsor affiliates, and recommend sites. Manage site activities to meet timelines and escalate issues with action plans.

Conduct on-site and remote site qualification, initiation, monitoring, management and close-out visits ensuring ICH/GCP and protocol compliance. Verify informed consent, perform source document and CRF review, manage IP accountability, reconcile ISF/TMF, document monitoring activities, support recruitment and audit readiness, and coordinate with sponsors and local staff. Role includes chart abstraction and real-world late phase activities where applicable.

The role involves site management activities in clinical trials, ensuring compliance with regulations, data accuracy, and effective communication with site personnel. It supports patient safety and recruitment, while managing site activities and documentation throughout the study lifecycle.

Performs site qualification, initiation, monitoring, management, and close-out visits ensuring ICH-GCP/GPP and protocol compliance. Reviews source documents, CRFs, IP handling, ISF/TMF reconciliation, documents findings, supports recruitment and audit readiness, and may perform chart abstraction for real-world studies.

Manage country-level site start-up activities including regulatory and ethics submissions, TMF document management, site activation, local regulatory intelligence, vendor management, and budget/contract support. Ensure SOP/WI compliance, track milestones, escalate delays, and support continuous improvement and training for site start-up processes.

Perform site qualification, initiation, interim monitoring, management and close-out visits (on-site or remote) ensuring ICH-GCP/GPP and protocol compliance. Verify informed consent and CRF/EDC data accuracy, conduct source document review, manage IP accountability, reconcile ISF with TMF, document monitoring activities, support recruitment/retention, and assist audit readiness. May perform chart abstraction and collaborate with sponsor affiliates; travel up to 75%.

Perform on-site and remote clinical site activities including qualification, initiation, monitoring, interim and close-out visits. Conduct source data verification, informed consent checks, IP accountability, ISF/TMF reconciliation, query resolution, and documentation. Support audit readiness, train/mentor junior CRAs, manage site communications, and contribute to study operational tasks. RWLP level includes chart abstraction, site identification, consent development, and input to RFPs and case report form design. Significant travel required.