Senior Scientist, Clinical Operations

Serve as the lead clinical scientist on the clinical trial team. Lead medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaboration with the Clinical Director. Collaborate cross-functionally in the development of the study protocol and related study materials (e.g., ICF documents / amendments). Partner with the Study Manager on study deliverables. Ensure CRF design supports data collection in alignment with the protocol in collaboration with Data Management/Programming. Collaborate cross-functionally to monitor clinical data to ensure quality, completeness, and integrity of trial conduct. Provide tactical/scientific mentorship to other clinical scientists. Must have a Bachelor's degree (or US equivalent) in Life Sciences plus 5 years relevant experience in pharmaceutical and/or clinical drug development or a Master's degree (or US equivalent) in Life Sciences plus 3 years relevant experience in pharmaceutical and/or clinical drug development. Must possess solid knowledge of clinical research regulatory requirements (e.g., GCP and ICH); ability to manage multiple competing priorities with good planning, time management and prioritization skills; and strong analytical skills with the ability to interpret clinical trial data and synthesize conclusions. Ability to interact with key stakeholders across department, division, and company; ability to provide a proactive approach, strategic thinking and leadership in driving toward study goals; and ability to influence opinions and decisions of internal and external customers/vendors, across functional areas, and within the division required. Must be able to apply leadership skills to processes, leading meetings, and influencing peers in a matrix environment. Must possess problem solving, prioritization, conflict resolution, and critical thinking skills; team building capabilities through proactive coaching; and strong communication, technical writing, and presentation skills. Telecommuting permitted. To apply, visit Merck Sharp & Dohme LLC's career site at www.merck.com/careers to create a profile and submit your CV for Job Req# R314381. EOE. Merck Sharp & Dohme LLC is a subsidiary of Merck & Co., Inc.