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As a Grant Specialist, you will manage grant applications, research funding opportunities, ensure compliance with requirements, and report on grant outcomes.

The Study Support Assistant provides administrative and operational support for clinical trials, including document preparation, meeting coordination, and compliance maintenance.

Responsible for executing recruitment strategies, managing the hiring process, utilizing data-driven insights, and promoting diversity in talent acquisition.

The Site Specialist II leads regulatory document preparation, coordinates with stakeholders, manages records, and supports study teams on regulatory compliance, enhancing study initiation efficiency.

The Clinical Research Associate (CRA) will oversee and coordinate clinical trials, ensuring compliance with regulations, and analyzing data while maintaining strong relationships with stakeholders and investigators.

The Clinical Research Associate II will conduct clinical trial visits, ensure compliance and data integrity, collaborate with investigators, and contribute to study documentation.

As a Senior CRA, you will oversee clinical trial activities, ensuring compliance with protocols and regulatory requirements, while supporting site staff and maintaining data integrity.

The Senior CRA will oversee clinical trial activities, ensuring compliance with protocols and regulatory standards, while managing site performance and relationships.

As a Principal Biostatistician, you will provide statistical services in analysis, design, and reporting, maintaining compliance with industry standards while overseeing clinical studies.

The Site Contracts Negotiator II negotiates and maintains clinical trial agreements, manages budgets, communicates with stakeholders, tracks contract progress, and identifies risks.