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

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

Manage day to day efforts and coordinate calendar of assigned team to ensure adequate pre and post sales support for designated products. Assist in setting of priorities where needed, based on business drivers. Learn the MACSima training process and support process to ensure the success of select priority customers with installation training and follow up support Work wit

Identify, profile and prioritize institutions and investigators involved in relevant clinical research activities. Execute sales activities within the assigned territory in accordance with corporate strategies and budget expectations. Meet and/or exceed company sales forecasts in assigned territory. Establish and maintain relationships with key investigators. Identify and