Responsible for the operational planning, feasibility, and execution of a clinical trial
May serve as the clinical trial team lead
May lead team in key study planning, development, and execution elements (e.g., data management deliverables, trial level plans/timelines, country/site selection, site materials, system updates, investigator meeting planning, communication plans, preparation of status update reports, study close out activities)
Leads team for timeline management, risk identification and mitigation, issue resolution
May facilitate and collaborate with key internal/external stakeholders (e.g., study team, country teams, vendors, committees) in support of clinical study objectives
Accountable for managing any study specific partners and/or vendors

Bachelor's Degree +5 years of pharmaceutical, clinical drug development, project management, and/or medical field experience OR Master's Degree +3 years of pharmaceutical, clinical drug development, project management, and/or medical field experience OR PhD/PharmD Degree
Degree in life sciences, preferred
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
Solid understanding of the principles of project planning & project management
Good analytical skills to drive operational milestones
Influence opinions and decisions of internal and external customers/vendors, across functional areas, and within the division
Intermediate knowledge in Microsoft office or similar (Excel, PowerPoint, Word, Outlook, etc.)

medical, dental, vision healthcare and other insurance benefits (for employee and family)
retirement benefits, including 401(k)
paid holidays
vacation
compassionate and sick days

Senior Scientist, Clinical Operations

Key skills