Regulatory Windchill Coordinator

Job Title: Regulatory Affairs Coordinator/Regulatory Windchill Coordinator Location: 91342, Los Angeles, California, United States Duration: 06 Month Job Description: This position is a shared role providing business support to the Medical Device division and collaborating with the Supply Chain Group, Regulatory Affairs, Clinical, and Customer Service. ...

Job Title: Regulatory Affairs Coordinator/Regulatory Windchill CoordinatorLocation: 91342, Los Angeles, California, United StatesDuration: 06 MonthJob Description:This position is a shared role providing business support to the Medical Device division and collaborating with the Supply Chain Group, Regulatory Affairs, Clinical, and Customer Service. Person...

Job Title: Regulatory Affairs Coordinator/Regulatory Windchill CoordinatorLocation: 91342, Los Angeles, California, United StatesDuration: 06 MonthJob Description:This position is a shared role providing business support to the Medical Device division and collaborating with the Supply Chain Group, Regulatory Affairs, Clinical, and Customer Service. Person...

Job Title: Regulatory Affairs Coordinator/Regulatory Windchill Coordinator Location: 91342, Los Angeles, California, United States Duration: 06 Month Job Description: This position is a shared role providing business support to the Medical Device division and collaborating with the Supply Chain Group, Regulatory Affairs, Clinical, and Customer Service. ...

Job Title: Regulatory Affairs Coordinator/Regulatory Windchill CoordinatorLocation: 91342, Los Angeles, California, United StatesDuration: 06 MonthJob Description:This position is a shared role providing business support to the Medical Device division and collaborating with the Supply Chain Group, Regulatory Affairs, Clinical, and Customer Service. Person...

Job DescriptionJob DescriptionDay to Day:This position is a shared role providing business support to the Medical Device division and collaborating with the Supply Chain Group, Regulatory Affairs, Clinical, and Customer Service.Person will help in getting products to market through the use of SAP/PLM system to create shipping licenses; will conduct clean-up...

Company Description Valiance Clinical Research is an interdisciplinary research center located in Los Angeles, California. We are focused on changing the future of healthcare through clinical trials. Our facility is equipped to perform clinical trials from Phase 1 studies to Phase 4. We prioritize ease of startup, efficient recruitment and retention, as well...

Company Description Valiance Clinical Research is an interdisciplinary research center located in Los Angeles, California. We are focused on changing the future of healthcare through clinical trials. Our facility is equipped to perform clinical trials from Phase 1 studies to Phase 4. We prioritize ease of startup, efficient recruitment and retention, as well...

DescriptionThe Department of Urology is seeking to hire a full time Clinical Trails Regulatory Coordinator to be responsible for regulatory coordination of clinical research studies within assigned units at the Institute of Urologic Oncology. Main responsibilities include: * Performing detailed review of clinical research protocols and utilizing that...

General Information Press space or enter keys to toggle section visibility Work Location: Los Angeles, USA Onsite or Remote Fully On-Site Work Schedule Monday - Friday 8am - 5pm (hours may vary) Posted Date 01/29/2024 Salary Range: $28.78 - 59.34 Hourly Employment Type 2 - Staff: Career Duration Indefinite Job # 12279 Primary Duties and...

General Information Press space or enter keys to toggle section visibility Work Location: Los Angeles, USA Onsite or Remote Fully On-Site Work Schedule Monday - Friday 8am - 5pm (hours may vary) Posted Date 01/29/2024 Salary Range: $28.78 - 59.34 Hourly Employment Type 2 - Staff: Career Duration Indefinite Job # 12279 Primary Duties and...

Description Under the direction of the Operational Managers, Investigators, Financial Administrative Office, Faculty, Medical and Administrative Directors of the Jonsson Comprehensive Cancer Center (JCCC) Clinical Research Unit (CRU) the Regulatory Coordinator is responsible for preparation, submission and maintenance of regulatory applications to fulfill...

DescriptionUnder the direction of the Operational Managers, Investigators, Financial Administrative Office, Faculty, Medical and Administrative Directors of the Jonsson Comprehensive Cancer Center (JCCC) Clinical Research Unit (CRU) the Regulatory Coordinator is responsible for preparation, submission and maintenance of regulatory applications to fulfill...

General Information Press space or enter keys to toggle section visibility Work Location: Los Angeles, USA Onsite or Remote Flexible Hybrid Work Schedule Monday - Friday, 8:00am - 5:00pm Posted Date 07/07/2023 Salary Range: $28.78 - 59.34 Hourly Employment Type 2 - Staff: Career Duration Indefinite Job # 7753 Primary Duties and Responsibilities Press space...

Job Description Job Description PureTek is a dynamic and innovative company specializing in developing and manufacturing pharmaceutical and cosmetic products. With a commitment to quality, safety, and regulatory compliance, we strive to deliver products that enhance the well-being and beauty of our consumers. Join our team and contribute to our mission of...

The UCLA CORE Kidney Health Program is seeking an experienced RegulatoryProject Manager to oversee all regulatory aspects of clinical trials, clinical programs,our patient and community outreach program, education and training, and assistwith administrative tasks. You will be responsible for the oversight ofregulatory coordination for clinical research...

Job DescriptionJob Description PureTek is a dynamic and innovative company specializing in developing and manufacturing pharmaceutical and cosmetic products. With a commitment to quality, safety, and regulatory compliance, we strive to deliver products that enhance the well-being and beauty of our consumers. Join our team and contribute to our mission of...

The role involves providing global regulatory oversight and project leadership for assigned development products, reporting directly to the Vice President of Regulatory Affairs. The incumbent will contribute to and execute regulatory strategies to facilitate global product development, oversee regulatory communications with health authorities, and ensure...

Position Summary The primary responsibility of the Regulatory Affairs Specialist is to manage and perform regulatory submissions for local and worldwide regulatory agencies. The RAS is also responsible for ensuring products and procedures comply with regulatory agency specifications. Supports necessary regulatory activities required for our client's product...

The Regulatory Affair Project Manager will oversee, manage and participate in startup research activities as part of the Translational Clinical Research Unit while under the direction of Financial Administrative Officer, Faculty Director, Medical Director, and Research Director (Senior Management) of the Jonsson Comprehensive Cancer Center Clinical Research...