Jobs at Syneos Health

Conducts site qualification, initiation, monitoring, management, and close-out visits for clinical and real-world studies. Ensures regulatory, ICH-GCP, protocol, data quality, informed consent, investigational product, and documentation compliance. Reviews source records, resolves queries, supports recruitment and retention, maintains trial files, documents site activities, trains study personnel, supports audit readiness, and communicates risks and action plans. Requires regular travel of up to 75%.

Conducts site qualification, initiation, monitoring, management, and close-out visits for clinical and real-world late-phase studies. Ensures regulatory, protocol, GCP, informed consent, data integrity, investigational product, and essential document compliance. Reviews source data, resolves queries, supports recruitment and retention, maintains audit readiness, documents site activities, and collaborates with sponsors and clinical teams. May train junior CRAs and support operational improvements, regulatory updates, and bid defense activities.

Conducts site qualification, initiation, monitoring, management, and close-out activities for clinical and real-world late-phase studies. Ensures regulatory, ICH-GCP, protocol, data quality, informed consent, investigational product, and documentation compliance. Reviews source records, resolves queries, supports recruitment and retention, maintains study files, prepares monitoring documentation, contributes to audit readiness, and collaborates with sponsors and project teams. May mentor junior CRAs and support operational improvements.

Conducts clinical trial site qualification, initiation, monitoring, management, and close-out activities. Ensures ICH-GCP, regulatory, protocol, informed consent, data quality, investigational product, and essential-document compliance. Reviews source records, resolves queries, supports recruitment and retention, maintains trial documentation, tracks site actions, contributes to audit readiness, and coordinates with sponsors and study teams. May support real-world late-phase studies, chart abstraction, site identification, staff training, and sponsor collaboration. Requires up to 75% travel.

Conducts clinical trial site qualification, initiation, monitoring, management, and close-out activities while ensuring GCP, regulatory, protocol, patient safety, and data integrity compliance. Reviews source documents, clinical data, investigational product records, and trial files; resolves queries; supports recruitment, audits, training, site communication, and project timelines. May support real-world late-phase studies through chart abstraction, regulatory coordination, site identification, and process improvement. Requires regular travel of up to 75%.

Manages country-level clinical trial site start-up activities, including regulatory and ethics submissions, essential document collection, site activation, milestone tracking, budget monitoring, and TMF filing. Provides country regulatory intelligence, supports site feasibility and selection, coordinates investigators and functional teams, and may assist with contract and budget negotiations. Ensures compliance with SOPs, work instructions, timelines, quality standards, and applicable local regulations.

Supports country-level clinical trial site start-up activities, including regulatory and ethics committee submissions, essential document collection, site activation, milestone tracking, budget monitoring, vendor coordination, and Trial Master File maintenance. Provides country regulatory intelligence, assists with investigator contracts and budgets, supports site feasibility and selection, and facilitates communication among investigational sites, project managers, and functional teams while ensuring compliance with SOPs, ICH GCP, and local regulations.

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.

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.