Communicate, correspond and interact with customers through a variety of traditional and digital channels. Follow specific standard operating procedures (SOPs) and work instructions while conducting all business related duties and transactions. Adhere to applicable ISO and compliance standards. Continuously fields a high volume of incoming emails / cases received through

Working with internal and external Data Management subject matter experts, coordinate and manage Data Management activities, timelines, and deliverables from study start to close out. Oversee CRO and vendors, and participate in study start up activities, including development, review, and approval of eCRF requirements, EDC database specifications, Data Transfer Specificat

Collaborate with Clinical Trial Manager(s) to assist in the operational and logistical aspects of clinical trial management tasks (e.g. start up, maintenance, and close out activities) according to ICH GCP and standard operating procedures. Liaise with CROs and other clinical vendors to ensure deliverables are met and communication is efficient. Partner with Investigators

Strategically plan for selection and optimization of the clinical biomarkers evaluations supporting clinical development within the therapeutic areas of the MBM interest. Provide review and analysis of company sponsored clinical studies for the assigned pharmaceutical products. Functionally contribute to planning of clinical trials acting as the expert for a scientific st

Manage the overall warehouse and materials management functions for designated site and business. Drive culture of safety and compliance through near miss reporting, safety/quality audits, operational metrics, and employee training. Hire, coach, develop, performance manage, and promote staff within assigned warehouse function. Provide goals, direction, and prioritization