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Clinical Trials Regulatory Specialist 1 Jobs

Quality And Regulatory Affairs Analyst - Genetics Clinical Trials
By Mount Sinai Health System At United States
Maintaining a working knowledge and thorough understanding of federal and institutional regulations and polices relating to human subjects research
2+ years of experience in clinical research
Experience using electronic regulatory platforms a plus
Experience with industry-sponsored clinical trials preferred
Conducting internal auditing and monitoring activities to ensure compliance with study protocols and applicable regulations
Assisting investigators and clinical research coordinators in preparing for site monitoring visits and audits
Regulatory And Economic Resources, Biologist 1
By Miami-Dade County At , $42,289 a year

Bachelors degree in Biology or related natural or environmental science field. Must possess a Driver license.

Travel & Trials Event Specialist
By Kirkland & Ellis At Los Angeles, CA, United States
Manage and effectively communicate Firm’s travel needs to vendors/resources.
Work on developing internal processes to enhance travel experience for attorneys and staff.
A minimum of 5 years of experience in travel or hotel sales and a Bachelor’s Degree.
Establishment and promotion of strong working relationships with external contacts and suppliers to ensure the Firm’s needs are understood and met.
Creation and dissemination of travel resource communication to the Firm.
Develop relationships with paralegals to assist with their trial related travel needs including contracting hotel guest room and meeting space.
Clinical Trials Regulatory Specialist 1
By Stanford University School of Medicine At Stanford, CA, United States
Experience in clinical trials operations, knowledge of clinical trials regulatory requirements, or experience working with an IRB.
Knowledge, Skills And Abilities (required)
Bachelor’s degree and three years of related experience or a combination of education and relevant experience.
Manage and oversee new study initiation process, including educating study staff and sponsors, resolving issues and providing regulatory guidance and support.
Excellent communication skills and superb attention to detail.
Experience with MS Office products and database applications required.