Clinical Trial Design Site Training Associate, Cork
Job Title: Clinical Trial Design Site Training Associate
We are seeking a highly skilled Clinical Trial Design Site Training Associate to join our global centre of excellence for clinical trials in Cork, Ireland.
About the Role:
The ideal candidate will have experience in clinical development and clinical trials cost forecasting. As Clinical Trial Design Site Training Associate, you will provide technical, project and operational expertise to support the strategy for various aspects within the clinical programs which may include site training, patient enrolment (recruitment & retention), and/or patient & researcher engagement (insights, education, and feedback).
Key Responsibilities:
* Support the established strategy for assigned area(s) of focus including site training, patient enrolment (recruitment & retention), and/or patient & researcher engagement (insights, education, and feedback).
* Partner with CTDC Consultant(s) and CDDA functions to deliver that strategy from identification to timeline development, pre-work, and post-deliverable follow-up.
* Create appropriate deliverables (e.g., training, educational materials) in partnership with CTDC Consultant(s) and functional content owners/vendors by communicating timelines, facilitating review meetings, and distributing outputs to cross-functional partners.
* Support internal systems and communication throughout the execution of project strategies.
* Maintain key platforms and systems in support of the CTDC team based upon assigned area(s) of focus.
* Upload and maintain eTMF records in compliance with requirements.
* Work closely with CTDC team members to evolve internal standards, processes, tools, and best practices.
* Demonstrate strong communication skills with external partners including clinical trial participants and health care professionals (HCPs).
* Contribute to a team culture valued for strategic and technical leadership.
Requirements:
* Bachelor's Degree in scientific or health-related field or equivalent.
* Minimum 3-5 years experience in the pharmaceutical industry.
* General understanding of trial/protocol design and its impact on overall site experience.
* Proven ability to deliver to timelines.
* Excellent communication skills with internal and external partners.
* Demonstrated organizational and critical thinking skills.
* Ability to lead and influence toward a common goal.
* Ability to leverage critical thinking and problem-solving skills to sustain strong relationships with key business partners and identify innovative process improvements.