As an Informed Consent Specialist, you'll develop, review, and ensure compliance of informed consent forms for clinical trials, collaborating with stakeholders, managing timelines, and acting as a subject matter expert.

The Project Support Analyst I provides assistance to clients, resolves inquiries, supports project management, and maintains project information confidentiality.

As a Project Manager, you'll lead global clinical trial site activations, manage study start-up planning, and ensure compliance with regulatory requirements while collaborating with stakeholders.

The Financial Analyst II manages project records in Oracle, collaborates with teams for data accuracy, reconciles financial data, and supports project closure activities.

Lead and manage projects as a Senior Statistical Programmer, focusing on analysis, programming, and validating datasets with CDISC ADaM standards, while offering mentorship and support.