USA Novartis Pharmaceuticals Corporation, East Hanover, NJ
Research & Development
You are applying to be part of the Novartis Talent Pool. We are not currently recruiting for this role but we are building a pipeline for future opportunities. If you would like to be considered for a similar position in future, then please submit your CV.
The Clinical Trial Associate will report into the US Pharma CDMA Head Clinical Operations and will be responsible for supporting the Clinical Operations Lead for a large Managed Access Program (Compassionate Use).
Objectives and key deliverables may include:
Tracking MAP requests and review/approval process
Assist in the management of the internal ICF review process
Interaction with foundation supporting drug supply shipments
Drug shipment tracking
Compiling MAP status update reports
Assisting with the internal review process
Attending Global MAP monthly meeting
Attending Local Team meetings
Additional responsibilities may include supporting the Clinical Trial Leads for Investigator Initiated Trials (IITs) and local US Phase IV trials, as well as the Clinical Operations Specialist with the clinical section of the NDA annual reports.
The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.
Key Must Have Competencies/Experiences:
- Ability to work with Microsoft office applications
- Good oral and written communication skills
- Healthcare/Sciences courses part of college program and an interest in the healthcare field
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considered, please do so. Applications for all positions are subject to each employer's specific requirements.