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.

Oversee and manage clinical trial activities ensuring adherence to protocols and regulations, with site monitoring and team collaboration.

As a Site Engagement Liaison, you will enhance site engagement by building relationships, supporting site staff with protocols, and optimizing performance metrics.

The Site Contracts Negotiator will handle the negotiation and maintenance of clinical trial agreements, ensuring compliance and effective communication with stakeholders.

The Clinical Research Associate will conduct clinical trial site visits, ensure compliance, and contribute to study documentation and data quality.

The Senior Clinical Trial Manager oversees clinical budgets, develops monitoring plans, drives enrollment, optimizes CRA performance, and maintains study integrity. They also manage relationships with stakeholders and mentor team members.

Conduct site visits for clinical trials, oversee trial conduct, maintain relationships with site staff, and ensure compliance with regulations.

As a Senior CRA, you will manage clinical trial activities, ensuring compliance with protocols and regulatory requirements while overseeing site performance and data integrity.

The Study Start Up Associate will lead the initiation of clinical trials by conducting feasibility assessments, site identification, and ensuring compliance with regulatory requirements.

As a Clinical Research Associate, you will conduct clinical trial monitoring, ensure protocol compliance, analyze data, and collaborate with site staff.

The Contract Analyst I will prepare and execute invoicing, manage client relationships, reconcile accounts, and support billing processes.

Lead and implement QA strategies for clinical trials, conduct audits and assessments, ensure regulatory compliance (ICH-GCP/FDA), review trial documentation and data, and mentor QA staff.

Support coordination and administration of clinical trials: maintain regulatory documentation, prepare study materials, liaise with cross-functional teams, and track trial metrics to ensure protocol compliance and smooth execution.

The Data Integration and Dashboard Lead coordinates and manages Real World Evidence projects, ensuring effective data integration and analytics for strategic decision-making in medical research.

Lead and develop the financial reporting team, ensuring compliance with US GAAP and local legislative requirements while managing monthly accounts and audits.

As a Senior Clinical Research Associate, you will monitor clinical trial sites, ensure compliance with protocols, and support site personnel in executing trials. Your role includes managing multiple sites, training staff, and upholding data integrity throughout the study lifecycle.

The Senior CRA will monitor clinical trial sites for compliance, conduct site visits, train site staff, and manage relationships with stakeholders in ophthalmology.

Develop and validate statistical programming code for clinical trial data analysis and reporting, ensuring data integrity and compliance with standards.

As a Clinical Trial Administrator, you will coordinate clinical trials, maintain documentation, support regulatory submissions, and facilitate cross-functional communication.

Manage, draft, review, and negotiate clinical research contracts; analyze terms and risks; advise project teams on compliance and contractual obligations; maintain records and improve contract management processes.