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The Senior CRA/Clinical Site Manager monitors clinical trial sites, ensuring adherence to guidelines, data integrity, and strong relationships with site staff while overseeing multiple clinical studies in Oncology.

As a Statistical Programmer, you'll develop and validate statistical programs for clinical trials, collaborate with teams, and ensure data integrity.

The Senior Investigator Pricing Analyst develops and analyzes pricing strategies for clinical trial investigators, collaborates with various teams, conducts financial analysis, and ensures compliance with regulatory requirements.

The Senior Contract Analyst will manage, review, and negotiate contracts for clinical research projects, ensuring compliance and contributing to innovative treatments.

Responsible for negotiating and maintaining clinical trial agreements, ensuring accuracy, compliance, and effective communication with study sites and internal stakeholders.

Manage and monitor clinical trial sites, ensuring compliance and quality data collection for phase I-IV trials. Train staff and conduct audits.

Oversee and manage clinical trial activities to ensure compliance with protocols, regulatory requirements, and industry standards. Conduct site assessments, monitor trials, and facilitate audits.

As a Clinical Research Associate II, you will oversee clinical trial processes, ensure data integrity, collaborate with sites, and prepare study documents.

As a Clinical Quality Compliance Lead, you will design quality management systems, lead audits, review clinical documents, and guide the compliance team.

Oversee planning, execution, and completion of clinical trials, ensuring compliance with timelines, budgets, and regulations while collaborating with teams and managing relationships.