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Job Description

An employer is seeking a Sterile Processing Department Training Manager for a long-term contract opportunity. This SPD Training Manager will collaborate with clinical trial coordinators to ensure proper handling of experimental instruments and medical devices, monitor staff competency and adherence to both standard and trial-specific sterile processing procedure and assist in identifying sterilization-related issues impacting the trials integrity. The SPD Training Manager will be joining a leader in the Medical Device industry to provide ongoing education and support for SPD staff regarding trial procedures and communicate SPD status & concerns with clinical research teams. This role can sit remote, but will require significant travel to US hospitals to assist in the training of SPD technicians to complete the sterilization and clinical trial studies. Other responsibilities will include: develop and implement training programs for SPD staff tailored to the needs of the clinical trial, maintain detailed documentation and training records to support regulatory compliance for trial audits, ensure sterilization protocols align with trial-specific research standards and regulatory requirements and following safety protocols for compliance within the trials sterilization practices.

We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to Human Resources Request Form (https://airtable.com/app21VjYyxLDIX0ez/shrOg4IQS1J6dRiMo) . The EEOC "Know Your Rights" Poster is available here (https://www.eeoc.gov/sites/default/files/2023-06/22-088\_EEOC\_KnowYourRights6.12ScreenRdr.pdf) .

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Skills and Requirements

5+ years of experience in clinical research compliance or supporting clinical trials

Strong knowledge of regulatory requirements (FDA, AAMI, CDC, Joint Commission)

Excellent communication and collaboration skills to liaise with clinical research teams

Ability to follow specialized training materials that reflect the trials unique sterilization needs

Open to significant domestic travel to hospitals Certification in Sterile Processing (CRCST, CIS, CHL) preferred null

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion,sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to [email protected].