Medical Affairs - Global Oncology
• Assist in the management of the day to day operations of clinical trials including coordination and oversight of all CRO/clinical site/vendor activities, liaison between Clinical Operations Manager and CRO, manage scopes of work/budgets/invoice payments.
• Assist in the management of the Trial Master File (submit documents, reconciliation, QC, etc.).
• Participate in development of protocol, case report form, CRF guidelines and other study documents.
• Prepare and/or review regulatory documents (e.g. ICF), contracts, requests for proposal.
• Ensure the training of CROs/investigators on protocol, regulatory, Eisai SOPs and data issues. Reviews and approves monitoring reports and ensures tracking of ongoing site issues. On-site Monitoring
• Minimum of college degree in a relevant discipline.
• Bachelor's degree in relevant scientific discipline preferred.
• CANDIDATES MUST HAVE MIN 3-5 years in-house in pharma company. Not just 3-5 years in CRO or onsite monitoring. We want to see associate in-house large pharma.
• Want to see experience in phase 1-3 global study trials in multifunctional areas.
• MUST HAVE experience in reviewing patient data and patient profiles.
• **Oncology Experience Highly Preferred.**
Best Regards,
Sneha Shrivastava
973-967-3348
Job details are sourced from the employer's original posting.
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Artech is an employer-of-choice for the last 25 years to over 7,500 consultants across the globe. We recruit top-notch talent for over 70 Fortune and Government clients coast-to-coast across the U.S., India, and China. We are #1 Largest Women-Owned IT Staffing Firm in the US and this may be your opportunity to join us! For more check: www.artechinfo.com