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19 Aug 2021

Temporary Clinical Scientist (21-25180)

iris.chen@axelon.com Summit, New Jersey, United States

Job Description

“This role is currently work-from-home and will move to the office environment after the COVID-19 restrictions are lifted.”

Job Description: Job Description: Remote until site is reopened
Must haves:
• 2+ years of experience working on clinical trials
• Previous role as a Clinical Scientist, or Clinical Manager/Study Lead
• Experience with writing study protocols
• Experience with clinical trial data review and cleaning
• Advanced Science degree (or additional years of experience if no advanced Science degree)

The Clinical Scientist function provides scientific expertise necessary to design and deliver clinical studies and programs.
• Will be responsible for design and execution of assigned clinical trial activities and work closely with clinical team members within the assigned project to execute activities associated with the conduct
• May serve as Clinical Trial Lead for one or more trials
• May lead or support trial level activities for one or more trials with the necessary supervision
• May co-lead study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team members
• Collaborate and liaise with external partners (e.g., KOLs)
• Seek out and enact best practices with instruction
• Provide regular and timely updates to manager/management as requested
• Develop Protocol and ICF documents / amendments and present these to governance committee and development team meetings as required
• Conduct literature review
• Submit clinical documents to TMF
• Develop site and CRA training materials and present these at SIVs and Investigator meetings
• Review clinical narratives
• Monitor clinical data for specific trends
• Develop Data Review Plan in collaboration with Data Management
• Ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programming
• Submit clinical contributions to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, PSUR, Orphan Annual Reports, HA, EC, IRB responses and contribute to regulatory submission.)

How to Apply

Please share Resumes to Iris.chen@axelon.com to apply.

Job Types: Temporary.

Job expires in 6 days.

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