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The Clinical Research Associate will manage site interactions, ensure compliance, monitor trials, track data, and facilitate training and recruitment for oncology studies.

The Clinical Research Associate will monitor oncology clinical trials, ensure compliance with regulations, support site training, and maintain documentation.

Negotiate, draft, review, and finalize clinical trial agreements, amendments, and ancillary documents with study sites. Maintain stakeholder communication, track contract progress in ICON/client systems, identify risks, support site start-up, file contractual documents, and participate in study team calls while adhering to SOPs and training requirements.

The Senior CRA manages clinical trial activities, ensures compliance with protocols and regulations, and supports site staff to maintain trial integrity.

The Senior CRA oversees clinical trial activities, ensuring compliance with protocols and regulatory standards, managing multiple sites, and providing training. Strong organizational and interpersonal skills are crucial.

Oversee site relationships and perform selection, initiation, routine monitoring, and close-out visits for oncology trials. Ensure ICH-GCP and regulatory compliance, maintain CTMS/eTMF documentation, monitor patient safety and drug accountability, support recruitment and data quality, escalate risks, and coordinate site payments and cross-functional partners. Travel up to 50% across the region.

The Senior Clinical Research Associate manages monitoring for cardiovascular clinical trials, ensuring compliance with FDA regulations and guiding teams to resolve site issues effectively.

Accountable for coordinating activities for site activations and maintenance, ensuring compliance with regulations and processes. Acts as a liaison, resolves issues, and supports project outcomes in clinical studies.

The Senior Clinical Research Associate will monitor cardiovascular devices, ensuring compliance with FDA regulations and managing study communication, while travelling regionally up to 65%.

Oversee clinical trial operations, manage cross-functional teams, ensure regulatory compliance, and handle budgets and timelines in early phase oncology studies.