Trial Capability Specialist

2 weeks ago

Cork, Cork, Ireland beBeeClinical Full time €50,000 - €70,000
Clinical Trial Associate Role

At a multinational pharmaceutical corporation, we unite innovation with discovery to make life better for people around the world. Our employees work together to develop and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.

Our diverse team delivers innovative solutions in various functions, including finance, information technology, medical, clinical trials, and more. We offer a premium workspace, complete with flexible working options, healthcare benefits, pension plans, and life assurance. The workplace is equipped with a subsidised canteen, onsite gym, travel subsidies, and on-site parking.

We have wellbeing initiatives, such as 'Enhancing Career Experience,' which enhance the career experience for our colleagues. Our organisation is committed to diversity, equity, and inclusion (DEI) with four pillars: Enable, EmbRACE, LGBTQ+, and GIN-Gender Inclusion Network.

Job Overview

The Clinical Trial Associate provides clinical trial capabilities in support of clinical development. The associate ensures investigator sites meet requirements to enroll study participants into clinical trials and supports ongoing activities during site maintenance and close-out.

Key Responsibilities
  • Initiate investigator site activities, including collection and submission of regulatory documents, customisation, and negotiation of informed consent documents.
  • 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.
  • Populate internal systems to ensure accuracy of trial/site performance.
  • Understand and comply 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.

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