- Parexel (Des Moines, IA)
- …Leader, Parexel!** In anticipation of future needs, we are seeking an additional Associate / Medical Director to join Parexel's highly recognized Medical ... our Global Immunology and Inflammation Therapeutic Franchise! As an Associate / Medical Director , you will work...any matters pertaining to safety of study participants and scientific integrity of the study + Attending and supporting… more
- Kemin Industries (Des Moines, IA)
- Overview Kemin Health is hiring an Associate Director of Regulatory / Scientific Affairs and Quality! In this role, you will be responsible for leading the ... to support the overall strategic plan + Work cross-functionally and provide regulatory , scientific and quality expertise and support through all stages… more
- Sumitomo Pharma (Des Moines, IA)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Regulatory Affairs (Oncology).** The Associate ... Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/She...degree in a related field required, preferably in a scientific discipline. + At least 7 years of experience,… more
- Kemin Industries (Des Moines, IA)
- Overview Kemin Nutrisurance is looking for an Associate Director of R&D to oversee our Antioxidants group! This influential role is responsible for steering the ... and managing the daily operations of the business unit's research team. The Associate Director will lead forward-thinking initiatives, define research goals, and… more
- Merck (Des Moines, IA)
- **Job Description** The Associate Director of Compliance will report to the Large Molecule Regional Quality Lead, Americas. The responsibility of this position ... compliance concerns. + Maintain up-to-date knowledge base with respect to emerging regulatory trends and changes in regulations and standards to incorporate into the… more
- Otsuka America Pharmaceutical Inc. (Des Moines, IA)
- ** Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and ... drug substance and drug product ensuring compliance with relevant ICH and regulatory guidelines + Develop and implement stability study protocols and timelines,… more
- Sumitomo Pharma (Des Moines, IA)
- …using SAS + Ability to generate documents / files required for regulatory filing. Ex. Reviewers' Guides, Define.XML, Annotated CRFs etc. + Executing Pinnacle ... 21 Checks + Knowledge about CDISC and Regulatory Guidelines + Demonstrate coaching skill to mentor Statistical...plus. + BS/MS or equivalent in Statistics, Math or Scientific Discipline The base salary range for this role… more
