• Support the company’s administrative routines, contributing to document organization, information updates, and support for internal processes; • Assist with commercial activities and customer relations, supporting registrations, record-keeping, and updating information in the systems and platforms used by the company; • Provide support for financial, tax, and operational routines, assisting with controls, entries, and monitoring the department’s requests; • Support the use and updating of the company’s internal systems and digital tools, contributing to information organization and activity tracking; • Participate in the learning and development of the company’s administrative routines, working alongside the administrative assistant and other support areas.

• Provides support to Clinical Data Management (CDM) project teams by performing various administrative activities • Runs test data for user acceptance testing during startup • Generates user acceptance testing data files post testing • Prepares study-specific metrics reports • Cleans patient tracker • Performs file reviews of the eTMF • Requests access to the electronic data capture (EDC) environment • Creates and maintains study information for CDM teams • Assists with validation of a client's coding dictionary subscriptions • Conducts quality control review of documents • Generates training completion reports • Files final versions of CDM documents

• Guide a team of Project Managers and support staff while serving as a strategic partner to pharmaceutical and biotech clients in their clinical trials journey. • Deliver excellence in project execution, client satisfaction, and team development as you oversee complex global clinical supply chain operations. • Support our mission of enabling customers to make the world healthier, cleaner, and safer by ensuring patients receive appropriate therapies when needed. • Establish and maintain strategic relationships with key stakeholders, coordinate cross-functional collaboration, and implement continuous process improvements. • Oversee portfolio management, resource allocation, and financial performance while supporting team members and cultivating a culture of excellence. • Apply your expertise in clinical trial operations and GMP environment to deliver outstanding service and maintain the highest quality standards.

• Draft, review, negotiate and finalize agreements with study sites • Ensure compliance to established negotiation parameters • Identify and assess legal, financial and operational risks • Coordinate with internal functional departments to ensure various site startup activities are aligned with contractual activities