Regulatory Operations Assistant – I
Integrated Resources, Inc ( IRI )California, United States
Posted March 3, 2017
Full Time
About the Company
Integrated Resources Inc. (IRI) is a leading professional staffing firm founded in 1996, specializing in contract, consulting, and full-time positions across Information Technology, Life Sciences, and Allied Healthcare. With a focus on quality and commitment, IRI offers comprehensive services including CRO clinical research, engineering management, and regulatory drug development. Their expert team of counselors partners with candidates and clients to find tailored solutions, distinguishing them in the industry through personalized service and extensive expertise.
Job Description
Integrated Resources, Inc. is seeking a Regulatory Operations Assistant - I to work on clinical trial disclosure and transparency activities, including registration and result posting on ClinicalTrials.gov and the EU Clinical Trial Register. The role involves working independently with close supervision and requires strong organizational skills, attention to detail, and proficiency in software tools such as Word, Adobe, and Excel.
Requirements
- 2+ years of experience in CLINICAL TRIAL DISCLOSURE & TRANSPARENCY ASSOCIATE
- 3-5 yrs in Biometrics, clinical operations, data management
- Requisite knowledge of clinical trial process
- Clinical Trial Manager, Clinical Data Manager, Clinical Trial Monitor – depends on strength of analytical skills