Global Clinical Trial Lead — Drive Timelines & Quality

Incyte Corporation; United States; On-site; USD 120,000 - 160,000; Full time

Job summary

Incyte Corporation, a global biopharmaceutical leader, seeks a Sr Clinical Trial Manager to drive execution of multinational trials. You will oversee timelines, budgets, feasibility, site selection, and vendor oversight, coordinating cross-functional teams to ensure compliant, timely delivery.

Responsibilities include protocol and regulatory document review, risk mitigation, data review, and recruitment planning, with meetings across study teams and stakeholders to optimize study conduct.

Qualifications

• BS/BA degree or equivalent with strong emphasis on science.
• Experience in biopharma or clinical research with multinational trials.
• Ability to manage complex/large trials.
• Working knowledge of ICH GCP and regulatory experience.
• Ability to manage multiple priorities across several protocols.
• Demonstrate leadership and problem solving skills.
• Experience in executing a wide range of clinical trial activities.
• Used to work in a multidisciplinary setting, strong collaborative team player.
• Good planning, prioritization, problem solving and organizational skills.
• Strong communication skills with stakeholders.

Responsibilities

• Deliver Trial(s) on time, within budget, and with high quality.
• Assist in review and writing of clinical trial documents (Protocol, CRFs, ICF, study report).
• Manage evaluation and selection of investigative sites; feasibility.
• Select, coordinate and monitor activities of vendors.
• Review monitoring reports and conduct co-monitoring visits as needed.
• Develop and manage trial timelines, budget and priorities.
• Participate in data review and discrepancy resolution.
• Ensure systems are in place to plan and implement trials and track progress.
• Generate reports to update management on trial progress.
• Ensure appropriate trial supply plans are implemented and managed.
• Develop recruitment and risk-mitigation plans; monitor contingencies.
• Participate in monitoring study safety.
• Develop study quality metrics and act with study team.
• Review CRO/vendor training on protocols and practices.
• Lead multi-disciplinary trial teams; manage study team meetings.
• Act as primary contact for trial between Drug Development and departments.
• Participate in working groups and special projects to improve operations.
• Ensure adherence to Good Clinical Practice and regulations.

Skills

Leadership

Budgeting

Trial management

Cross-functional teamwork

Education

BS/BA in science

Job description

Incyte Corporation, a global biopharmaceutical leader, seeks a Sr Clinical Trial Manager to drive execution of multinational trials. You will oversee timelines, budgets, feasibility, site selection, and vendor oversight, coordinating cross-functional teams to ensure compliant, timely delivery.

Responsibilities include protocol and regulatory document review, risk mitigation, data review, and recruitment planning, with meetings across study teams and stakeholders to optimize study conduct.