Job Title: Clinical associate consultant
Location: Bridgewater, New Jersey, Hartford, CT
Job Type: Permanent
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.
- Experience and detailed understanding of Products like Veeva.
- At least 2 Years of experience in information technology.
- 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