Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Manages all aspects of assigned clinical trials involving patient and healthy subject populations in both inpatient and outpatient settings. Acts as liaison between functions (i.e. PM, investigator, research team, etc.). Ensures client requirements and specifications are communicated to the research teams and any issues/questions raised by the research team or investigators are communicated back to the project leads and clients (as needed) for resolution.

 

Qualifications:

Bachelor's degree or equivalent and relevant formal academic / vocational qualificationPrevious experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years)Knowledge of Phase 1 processes and strong knowledge of clinical study operationsKnowledge of FDA regulations and ICH GCP guidelinesSolid computer skills with working knowledge of Microsoft Office applicationsGood time management and multi-tasking skillsSolid written and verbal communication skillsStrong organizational and prioritization skills with the ability to prioritize workload and adapt to changing study needsFavorable consulting skills to act as a liaison between external and internal groupsKnowledge of budgeting/forecasting/planning projects