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The Data Management Lead will oversee clinical trial data activities, manage project timelines, engage stakeholders, and ensure high-quality, compliant data in oncology studies.

Support clinical/scientific conduct of studies including medical monitoring, adjudication support, imaging reconciliation, protocol deviation management, and stakeholder liaison. Prepare meeting materials and ensure compliance with GCP and company processes.

As Global Head of Inside Sales, you'll develop and execute a global sales strategy, enhance market presence, and lead a high-performing team to drive growth across business units, ensuring alignment with corporate objectives.

The Senior Clinical Research Associate is responsible for site management and monitoring for clinical trials, ensuring compliance with regulations and quality. They serve as the main contact for investigator sites, manage investigator relationships, handle protocol-related issues, and oversee site performance on assigned trials.

The Business Operations Analyst supports Clinical Operations with contract management, financial planning, data analysis, and facilitates cross-department collaboration, ensuring documentation accuracy and efficiency improvements.

The Sr. Clinical Research Associate manages sites for clinical trials, ensuring compliance with protocols and regulations, conducting monitoring visits, and collaborating with study teams.

Lead global study start-up and site activation for Phase I-III and real-world trials. Develop global start-up plans, partner with CROs and stakeholders, forecast enrollment, track KPIs, remove activation barriers, and mentor junior staff to ensure timely, high-quality study delivery.

Manage design, configuration, launch, monitoring, and close-out of electronic feasibility surveys. Ensure site/investigator readiness, maintain contact lists, track responses and CDAs, apply site identification strategy, and support risk mitigation for global feasibility assessments.

The Principal Biostatistician provides statistical support for clinical trials, leads analyses, and contributes to regulatory compliance and client meetings.

The Senior Clinical Research Associate oversees site management and monitoring for clinical trials, ensuring compliance with GCP, patient safety, and quality execution of studies. Responsibilities include managing operational aspects, training site personnel, addressing protocol issues, and conducting monitoring activities.