Top Tech Jobs & Startup Jobs in Austin, TX

The Senior Clinical Research Associate manages study sites, ensuring compliance with regulations and high performance. Responsibilities include site selection, monitoring, training site staff, and data management.

Lead strategic regulatory input for small molecule products, ensure compliance with global regulations, prepare documentation, and collaborate cross-functionally.

The Senior/Vice President, Technical will lead regulatory strategy initiatives, advise clients on product lifecycles, and represent Parexel as an industry thought leader while mentoring colleagues.

Lead execution of complex publication programs in medical communications, manage projects, budgets, timelines, and collaborate with teams to ensure successful delivery.

The Consultant will provide statistical expertise in meta-analysis, collaborate on evidence generation plans, and guide junior staff in a multi-disciplinary research environment.

Lead the data management team in clinical trials and medical affairs, ensuring quality data, project oversight, stakeholder engagement, and compliance with standards.

The Sr. Clinical Research Associate is responsible for site management and monitoring of clinical trials to ensure patient safety and compliance with regulations.

The Proposals and Contracts Specialist manages the proposal and contract processes, develops client-specific standards, handles negotiations, and ensures quality deliverables within strict deadlines.

The General Manager oversees FSP programs, ensuring high-quality service delivery, financial management, account growth, and operational excellence, while maintaining customer relationships.