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The VP of Advertising & Promotional Review leads compliance and regulatory advisory services, manages promotional review processes, and collaborates with C-suite executives in pharmaceutical and biotech sectors.

The Project Manager is responsible for tracking an investigation burndown plan, holding daily meetings with investigators, and ensuring execution of tasks while escalating issues to upper management.

The Audit Coordinator manages the Quality & Compliance Audit Program, supporting Project Managers with document generation, contract communication, project reporting, and administrative tasks.

The Information Specialist manages health and safety calls, records data, documents adverse events, and provides product safety information, ensuring quality customer service and escalation when necessary.

The Vice President, Nonclinical Emerging Therapies oversees regulatory activities for therapeutic products, interfacing with clients, ensuring timely submissions, and leading teams in regulatory discussions with agencies.

The Central Study Coordinator coordinates remote site activities for assigned projects, manages communications, supports recruitment, handles data entry, and ensures compliance with regulations.

The Finance Intern assists in analyzing financial data, preparing reports, and supporting budgeting processes while collaborating on month-end activities and maintaining financial records.

The intern will support sales enablement and research, conducting analysis on clients, buyer groups, and market dynamics to aid in strategic account planning and client engagement efforts.

The position involves auditing pharmacovigilance processes with a focus on ensuring compliance and quality. Requires over 10 years of relevant experience.

Responsible for coordinating and supporting remote site activities for clinical research projects, including recruitment, documentation, and communication with study sites.