Director of Medical Monitoring, Clinical Affairs - GI
Director of Medical Monitoring, Clinical Affairs - GI
EG Life Sciences (now Eliassen Group)
United States
See who EG Life Sciences (now Eliassen Group) has hired for this role
Our F500 Pharma client is seeking a Director of Medical Monitoring to lead cross project clinical research activities to support development, approval, and commercialization. The role will be responsible for developing clinical strategies of multiple clinical trials of varying size and complexity to support regulatory submissions within the US and globally. The position will work in close collaboration with R&D, Regulatory, Clinical Operations, Medical Affairs, Marketing, Quality, Data Management, and Biostatistics.
RESPONSIBILITIES
• Provide strategic input of programs; guide clinical science of programs from study design and protocol development through completion of final study report and regulatory filings.
• Participate in Investigator selection, recruitment, and training; Interacts with Investigators and study sites during study conduct.
• Plan and create written and oral presentations of clinical study information; participate in Investigator’s Meetings; reports clinical study results to senior leadership as needed.
• Collaborate with and influences R&D, Quality, Clinical Operations, Regulatory and other leaders around product improvements, technologies, intellectual properties, and other clinical issues.
• Collaborate with Marketing to develop and identify studies to support commercial operations.
• Foster relationships with top scientific key opinion leaders.
• Provide effective input for promotional review committees.
• Support the R&D organization as a medical monitor and medical expert for clinical studies.
• Ensure that sponsored clinical trials are executed in accordance with Food and Drug Administration (FDA) regulations, Institutional Review Board (IRB) approval, and Good Clinical Practices (GCPs).
• Plan and assist with the preparation of regulatory submissions (e.g., INDs, NDAs, IDEs, PMAs, and PMA supplements).
• Partner with Data Management and Biostatistics to ensure that clinical studies are properly planned, performed, and analyzed.
• Interact with investigational sites, clinical consultants, Contract Research Organizations, and other vendors.
MUST HAVES – QUALIFICATION SUMMARY
- MD required
- 5-10 years minimum of GI experience in Crohn’s, IBD/IBS, ulcerative colitis
- Pharmaceutical industry experience with leadership experience in clinical trials/research
- Proven track record of successfully in designing, planning, and executing clinical studies
- Experience with Medical Monitoring and oversight of Medical Monitors
- Strong communication (oral and written) skills including publications, regulatory documents, and presentations
- Executive Communication/Presentation; communicate and present at the executive level: proficiency in stakeholder buy in, strong cross functional communication, organizational navigation, building rapport across functions and levels of management
NICE-TO-HAVES
Global pharmaceutical product development experience
TRAVEL & LOCATION
Remote but willing to accommodate East Coast Hours
START & TERM
Immediate. 6-month initial contract with strong likely hood to extend for several years
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Seniority level
Director -
Employment type
Full-time -
Job function
Product Management, Project Management, and Strategy/Planning -
Industries
Biotechnology Research and Pharmaceutical Manufacturing
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See who you knowFeatured Benefits
Inferred from the description for this job
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Medical insurance -
Dental insurance -
Vision insurance
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