Location: Remote, USA
Type: Full Time Permanent
Established Biopharmaceutical company on the East Coast
12 month and renewable contract
Trials spanning Phases II and III
Collaborate cross functionally (clinical dev, regulatory, clinical ops, data management, etc.) to design clinical trials
Author SAP and contribute to statistical sections of trial protocols
Offer statistical guidance on conduct of ongoing clinical trials
Work with statistical programmers in the summary and analysis of data
Contribute to regulatory documentation in support of regulatory submissions
Contribute to scientific articles, summarizing data collected
Add value to departmental standards & SOPs, in support of senior management
Manage CRO outsourced work
Minimum Masters in related subject
Excellent written and oral communication presentation skills
Experience working with SAS
Knowledge of CDISC data standards
Any exposure to health authority interactions will be viewed positively
I manage a range of other permanent and contract positions for a broad portfolio of clients (Biotech, CRO and Pharma). If the above role isn’t for you but you’d nevertheless like to discuss your options in the market, I’d welcome a confidential discussion by phone or email. Contact Daniel Cheetham at (617) 982 1238.
Salary: Strong hourly rate
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