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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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