Job Details

A company is looking for a Clinical Trials Specialist to manage protocol teams in clinical trials related to HIV and other infectious diseases.Key ResponsibilitiesLeads protocol development, study start-up, and study conduct activitiesDevelops and manages study-specific ancillary documents and communicates study progressPartners with cross-functional teams and resolves issues encountered during all study phasesRequired QualificationsMaster's degree in public health, social sciences, or related discipline preferred, with two years of relevant experienceBachelor's degree may be accepted with five years of relevant experienceExperience leading protocol development and writing clinical research protocols is requiredExperience with HIV, hepatitis, and/or tuberculosis trials is preferredStrong organizational skills and ability to manage multiple tasks simultaneously