Overview
Skills
Job Details
Clinical associate consultant
Bridgewater, New Jersey, United States
Job Description
Required Qualifications:
Bachelor s degree or foreign equivalent required from an accredited institution. Will also consider three years of progressive experience in the specialty in lieu of every year of education
At least 2 Years of experience in information technology.
Experience and detailed understanding of Products like Veeva.
End-end Clinical trial management process and related applications.
Experience/knowledge on clinical reporting (internal, FDA) during study start to closeout phases.
Experience/knowledge in Computer systems Validation activities
Familiarity with Good Clinical Practices, Good Documentation practices, Clinical Trial Quality & Compliance.
Good Knowledge of Study life cycle activities (Study Protocols /study design for IRT and EDC Studies), various study milestones, clinical trial regulatory reports and other metrics reports at study level /site level.
Basic- Must be able to translate business requirements into well-formed technical and system requirements
Basic Experience with modeling business processes, data flows, and workflow processes depicting relationships between Clinical data entities.
Agile Scrum.
Strong oral & written communication skills, Business stakeholder management
Must have performed business requirement analysis, use case modeling from a business analysis/consulting standpoint.
Experience in the full System Development Life Cycle (SDLC) on a variety of technologies and platforms preferably in pharma IT space
Preferred Qualifications:
Experience and desire to work in a management consulting environment that requires regular travel
Planning and Co-ordination skills
Good Communication and Analytical skills