The Senior Clinical Study Lead (CSL) is expected to operate with a high degree of independence and accountability for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out.
Responsibilities
Leads the cross-functional study team responsible for clinical study delivery and is the primary point of contact for leadership and oversight for the assigned study Provides operational input into protocol development Oversees and provides input to the development of study-specific documentation Ensures compliance with clinical trial registry requirements Identifies outsourcing needs of the study and leads and oversees engagement, contracting, and management of required vendors Provides input into baseline budget development and management Leads risk assessment and identifies risk mitigation strategies at the study level Monitors progress for site activation and monitoring visits and acts on any deviations from plan This role has a 3-day onsite minimum requirement in our Dublin office. This role is NOT eligible for fully remote. Requirements
Exceptional interpersonal & leadership skills Applies advanced expertise and implements the operational strategic direction and guidance for respective clinical studies Demonstrates expert knowledge and a data-driven approach to planning, executing, and problem-solving Advanced communication skills via verbal, written, and presentation abilities Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization Ability to influence and negotiate across a wide range of stakeholders Strong budget management experience An awareness of relevant industry trends Ability to build, lead, and develop productive study teams and collaborations Applies advanced negotiation and interpersonal skills to vendor management Technical proficiency in trial management systems and MS applications Does this sound like you? Salary: $150,000 - $200,000 per year
Leads the cross-functional study team responsible for clinical study delivery and is the primary point of contact for leadership and oversight for the assigned study Provides operational input into protocol development Oversees and provides input to the development of study-specific documentation Ensures compliance with clinical trial registry requirements Identifies outsourcing needs of the study and leads and oversees engagement, contracting, and management of required vendors Provides input into baseline budget development and management Leads risk assessment and identifies risk mitigation strategies at the study level Monitors progress for site activation and monitoring visits and acts on any deviations from plan This role has a 3-day onsite minimum requirement in our Dublin office. This role is NOT eligible for fully remote. Requirements
Exceptional interpersonal & leadership skills Applies advanced expertise and implements the operational strategic direction and guidance for respective clinical studies Demonstrates expert knowledge and a data-driven approach to planning, executing, and problem-solving Advanced communication skills via verbal, written, and presentation abilities Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization Ability to influence and negotiate across a wide range of stakeholders Strong budget management experience An awareness of relevant industry trends Ability to build, lead, and develop productive study teams and collaborations Applies advanced negotiation and interpersonal skills to vendor management Technical proficiency in trial management systems and MS applications Does this sound like you? Salary: $150,000 - $200,000 per year
