- Lilly (Durham, NC)
- …this position is $63,000 - $162,800 **Position Brand Description:** The EM associate assists in the safe, compliant execution of the environmental monitoring (EM) ... environmental monitoring, sterility assurance validation, microbiology laboratory, technical services/MSAT, quality assurance, etc.) + Strong self-management and organizational skills… more
- IQVIA (Durham, NC)
- …and mentor current scientific staff in business development efforts, to mentor senior - and mid-level scientific staff, and assists in developing team best practices ... processes for COA Consulting services; training and mentoring Associates, Associate Consultants, Consultants, and Managers in these Project Management processes… more
- Abt Global Inc. (Durham, NC)
- …candidate will join our Research, Monitoring, and Evaluation (RM&E) Capability. As a Senior Associate in RM&E, you will conduct research, monitoring, and ... Solving the world's most pressing issues and improving the quality of life for people worldwide is what we...other research designs. This includes demonstrated success as a principal investigator or project director, in business development, and… more
- Abt Global Inc. (Durham, NC)
- **World at** ** ** **Abt** Solving the world's most pressing issues and improving the quality of life for people worldwide is what we do every day at Abt. Creating a ... in the development and use of CMS's health care quality measures, quality improvement and provider rating...experienced technical staff who are in such roles as Principal Investigator, Technical Project Director, Director of Analysis, and… more
- IQVIA (Durham, NC)
- …processes and positive client interactions. In addition, perform the duties of Principal / Sr . Biostatistician for projects as needed. This position sits under ... Manage staffing of projects and coordinate task assignments. Responsible for the quality and completion of projects within Biostatistics. Help to ensure growth of… more
- IQVIA (Durham, NC)
- The Associate Director, Principal Medical Writer is responsible for the development of clinical documents for submissions to regulatory authorities globally. ... and leadership to other writers to ensure the timely delivery of high quality documents that are scientifically rigorous, logically organized, and have accurate data… more