- Edwards Lifesciences (Dover, DE)
- …the requirements of the Associate Manager Required + Experience in clinical trial design, indication lead + FDA/EMEA/PMDA submission experience + The ... + Act as core team member/lead biostatistician of assigned clinical trial (s) in US and international/global ...trials with skill levels exceeding the requirements of the Associate Manager Required or + Master's Degree or equivalent… more
- Astrix Technology (Dover, DE)
- …space. + Working knowledge of Clinical & Regulatory systems such as Clinical Trial Management System (CTMS), electronic Trial Master Files (eTMF), ... for the sale and growth of Astrix Technology Group's Clinical and Regulatory Consulting services to a portfolio of...representative of those that must be met by an associate to successfully perform the essential functions of this… more
- Merck (Dover, DE)
- …and retention efforts to achieve study milestones + Upon request from Global Clinical Trial Operations (GCTO), + Recommends study sites and identifies potential ... **Job Description** The Regional Medical Scientific Associate Director is a credentialed (ie, PhD, PharmD,...Maintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI)… more
- Takeda Pharmaceuticals (Dover, DE)
- …documents such as Briefing Books (BB), Investigational New Drug Applications (INDs), Clinical Trial Applications (CTAs), Investigator's Brochures (IBs), New Drug ... the best of my knowledge. **Job Description** **About the role:** ** Associate Director, Nonclinical Regulatory Writing and Submission Support,** **_Oncology and… more