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The Project Manager for Early Phase leads teams, manages sponsor communication, oversees project implementation, and ensures compliance with regulations. They handle budgets, timelines, and risk management while ensuring operational excellence in clinical trials.

The role involves developing site start-up strategies, overseeing documentation, managing site activities, and collaborating with cross-functional teams to ensure timely execution of clinical studies.

The Global Site Start-up Lead is responsible for the efficient execution of site activation for clinical trials, developing site start-up strategies, managing CROs, ensuring proper documentation, and leading process improvements with cross-functional teams.

The Business Analyst role at Parexel involves contributing to the development of therapies through various clinical development solutions, ensuring alignment with the company's values.

The Regulatory Affairs Consultant will lead a team to manage regulatory strategies and support product launches in Hong Kong, ensuring compliance and collaboration with local stakeholders.

The Biostatistician II role involves data production, statistical analysis, project coordination, client interaction, mentoring, and business development support.

The Senior / Principal Statistical Programmer leads statistical programming for clinical trials, providing expertise and monitoring quality, timelines, and resource allocation while mentoring a global team.

Develop and QC clinical-derived datasets (SDTM, ADaM), tables, figures and listings using SAS; assist project start-up, maintain documentation and regulatory compliance, and provide training/mentorship.

Responsible for managing clinical trial sites, ensuring compliance with regulations, training staff, and performing monitoring activities to support study success.

The role involves managing clinical trial budgets and contracts, negotiating with stakeholders, and ensuring compliance with regulations. Responsibilities include budget development, contract negotiations, and cross-functional collaboration to optimize clinical research support.