Clinical Trial Specialist

2 weeks ago


Cork, Cork, Ireland beBeeClinicalTrial Full time €60,000 - €100,000
Clinical Trial Specialist

Eli Lilly Cork is a global healthcare leader that unites caring with discovery to make life better for people around the world.

We are headquartered in Indianapolis, Indiana, and our employees work together to discover and bring life-changing medicines to those who need them.

We are committed to diversity, equity, and inclusion (DEI) and cater to all dimensions, ensuring the inclusion of all ethnicities, nationalities, cultural backgrounds, generations, sexuality, visible and invisible disabilities, and gender.

The Trial Capabilities Team provides clinical trial capabilities in support of clinical development. As a Clinical Trial Specialist, you will be accountable for ensuring investigator sites meet requirements to enroll study participants into clinical trials and supporting ongoing activities during site maintenance and closeout.

Key Objectives/Deliverables:

  • Clinical Trial Capabilities Responsibilities

• Initiate investigator site activities, including collection and submission of regulatory documents, customization and negotiation of informed consent documents, serve as the point of contact for a site's ERB and Competent Authority (CA), supervise and ensure site compliance to required training, and effectively drive timelines aligned with company priorities.

• Communicate directly with sites to enable start-up and maintain an active collaboration with sites during maintenance and close-out.

• Identify, communicate, and resolve issues.

• Ensure country-specific regulatory and data privacy requirements are incorporated into submission documents and any other documents/systems.

• Leverage previous site/review board engagements to efficiently drive new work.

• Populate internal systems to ensure accuracy of trial/site performance.

• Understand and align with procurements, legal, and financial requirements and procedures.

• Populate Trial Master Files and libraries for future reference.

• Provide feedback and shared learning for continuous improvement.

• Leverage trial prioritization.

• Anticipate and monitor dynamically changing priorities.



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