Clinical associate consultant

Overview

On Site
$120,000 - $140,000
Full Time
10% Travel

Skills

Clinical Practices
FDA
clinical reporting
Veeva

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

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