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Clinical Trial Design Site Training Associate, Cork Client:
Location: Cork, Ireland
Job Category: Other
EU work permit required: Yes
Job Reference: 81416bac9d91
Job Views: 160
Posted: 21.01.2025
Expiry Date: 07.03.2025
Job Description: Clinical Trial Design Site Training Associate
Our client, a global pharma organisation, is currently recruiting for a Clinical Trial Design Site Training Associate to join their global centre of excellence for clinical trials on a permanent basis.
The ideal candidate will be experienced in clinical development and clinical trials cost forecasting.
This is a hybrid working role.
As Clinical Trial Design Site Training Associate, you will provide technical, project and operational expertise to support the strategy for a variety of aspects within the clinical programs which may include site training, patient enrolment (recruitment & retention), and/or patient & researcher engagement (insights, education, and feedback).
Responsibilities: Support the established strategy for the assigned area(s) of focus of site training, patient enrolment (recruitment & retention), and/or patient & researcher engagement (insights, education, and feedback).
Partner with the CTDC Consultant(s) and appropriate Clinical Design Delivery & Analytics (CDDA) functions to deliver that strategy from identification to timeline development, pre-work, and post-deliverable follow-up.
Support the creation of the appropriate deliverables (e.g., training, educational materials) in partnership with the CTDC Consultant(s) as well as the functional content owners and/or vendors by communicating timelines, facilitating review meetings, and distributing outputs to cross-functional partners.
Support internal systems and communication throughout the execution of the project strategies.
Understand specific capabilities and access points to maintain key platforms and systems in support of the CTDC team based upon the assigned area(s) of focus.
Upload and maintain eTMF records in compliance with the requirements.
Work closely with CTDC team members to continue to evolve internal standards, processes, tools, and best practices.
Demonstrate strong communication skills, both verbal and written, with external partners including clinical trial participants and health care professionals (HCPs).
Work with external contracting of vendors, patients, and HCPs.
Contribute to a team culture that is valued for strategic and technical leadership.
Provide technical support to ensure that processes for the assigned area(s) of focus are well integrated within the appropriate CDDA functions.
Support the delivery of right-sized strategies that can be successfully implemented in the clinical programs.
Requirements: Bachelor's Degree in scientific or health-related field or equivalent.
Minimum of 3-5 years experience in the pharmaceutical industry.
General understanding of trial/protocol design and how that impacts overall site experience.
Proven ability to deliver to timelines.
Excellent communication (written and verbal) 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.
Ability to thrive in a highly collaborative team environment, both in person and through virtual connections.
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