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The Safety & Pharmacovigilance Coordinator monitors safety information, performs data entry into safety databases, assists with case file management, and ensures compliance with regulations. This role supports safety submission processes and documentation, requiring teamwork and attention to detail.

The role involves managing resource solutions, conducting stakeholder meetings, supporting demand planning, maintaining data integrity in resourcing tools, and assisting with recruitment efforts.

The Clin Ops Specialist conducts compliance activities, assists with site management, maintains clinical documentation, and coordinates supplies and meeting logistics.

The role involves leading programming efforts, developing SAS code to generate statistical outputs, ensuring quality standards, and providing mentorship on complex projects in clinical trials.

The Project Specialist at Syneos Health will collaborate on biopharmaceutical projects, support customer success, and contribute to clinical development initiatives within a diverse team.

The Principal, Global Feasibility leads complex RFPs and feasibility evaluations, collaborates across teams, mentors junior members, ensures high standards, and conducts research for assessments.

Manage and coordinate Phase 1 clinical research studies, ensuring compliance, communication, logistics, and documentation throughout the trial process.

Conduct on-site and remote monitoring of clinical research studies, ensuring compliance with GCP guidelines, managing project components, and collaborating with teams to support clinical trial operations.

Conduct monitoring of clinical research studies for compliance, develop monitoring tools, manage project components, and collaborate with teams for effective trial operations.

Oversee interdisciplinary clinical research studies ensuring compliance with GCP and regulatory requirements, manage project finances, and lead project teams for successful delivery.