Clinical Trial Coordinator

3 days ago

Cork, Cork, Ireland beBeeClinical Full time €51,304 - €73,344
Job Description">

We are seeking a skilled professional to provide clinical trial capabilities in support of clinical development. The successful candidate will be responsible for initiating investigator site activities, collecting and submitting regulatory documents, communicating with sites, and ensuring country-specific regulatory requirements are incorporated into submission documents.

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Main Responsibilities:

  1. Initiate investigator site activities, including collection and submission of regulatory documents
  2. Communicate directly with sites to enable start-up and maintain an active collaboration with sites during maintenance and close-out
  3. Identify, communicate, and resolve issues
  4. Ensure country specific regulatory and data privacy requirements are incorporated into submission documents
  5. Leverage previous site / review board engagements to efficiently drive new work
  6. Populate internal systems to ensure accuracy of trial / site performance

As part of this role, you will need to understand and comply with legal and financial procedures.

">Required Skills and Qualifications:">

The ideal candidate will possess strong communication and organizational skills, as well as the ability to work effectively in a team environment. They should also have experience in clinical trials and a thorough understanding of regulatory requirements.

">Benefits:">

This is an exciting opportunity to join a dynamic team and contribute to the success of our organization. As a member of our team, you can expect a competitive salary and benefits package, as well as opportunities for career growth and development.

">

We offer a collaborative and inclusive work environment that values diversity and promotes equal opportunities. Our company culture is built on the principles of integrity, respect, and open communication.

">Purpose of the Role:">

The purpose of this role is to provide clinical trial capabilities in support of clinical development. This includes providing administrative support, managing site interactions, and ensuring compliance with regulatory requirements.

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