- Kelly Services (Thousand Oaks, CA)
- …and public presentations, collaborating closely with cross-functional teams and CRO partners to achieve program milestones. **Responsibilities** Leadership & ... engineering workflows, ensuring efficient resource allocation, timeline adherence, and risk management . + Inspire and guide junior scientists, setting high data… more
- IQVIA (Durham, NC)
- …you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These sponsor ... experts. + Write statistical analysis plans. + Monitor internal and CRO project activities including timelines, deliverables, and availability of resources. +… more
- University of Rochester (Rochester, NY)
- …experience in clinical research environment; (medical, laboratory, clinical supplies, data management , CRO , etc.) promoting a service to key high-level ... new clinical trials business opportunities with Contract Research Organizations ( CRO ), pharmaceutical companies, biotech companies and other academic institutions. -… more
- BeOne Medicines (San Mateo, CA)
- …scientific expertise for selection of investigator and vendors. + Train BeOne colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or ... clinical trial; respond to clinical questions from sites, IRBs/IECs, Health Authorities, and CRO 's + Review, query, and analyze clinical trial data. + Interpret, and… more
- Charles River Laboratories (Mattawan, MI)
- …performing detailed maintenance (PM/CM) on physical plant equipment, full automation control of facility plant equipment, and general maintenance activities as ... and compressors. * Operating Building Automation Systems (BAS) and equipment control systems. * Provides mentoring/training to other technicians with respect to… more
- IQVIA (Durham, NC)
- …get all the benefits of working for an industry leading global CRO while collaborating directly with expert cross-functional sponsor teams. Sponsor clients include ... experts. + Write statistical analysis plans. + Monitor internal and CRO project activities including timelines, deliverables, and availability of resources. +… more
- IQVIA (Durham, NC)
- …of the Sales organization - FSP services for the Data Management , Biostatistics, Programming, Medical Writing, Lifecycle Safety, and Regulatory Affairs functions ... + 10 years related experience, including 3 years of relevant industry ( CRO /Pharmaceutical) and/or sales experience Req Or + Equivalent combination of education,… more
- University of Pennsylvania (Philadelphia, PA)
- …forms and study binders required by sponsor or Clinical Research Organization ( CRO ) as directed by Supervisor, Clinical Research Nurse (CRN), or Clinical Research ... * Assists in resolving regulatory related queries with, IRB, CRO and sponsors * Performs related duties as assigned...tools, preparing for internal and external audits + Data management and entry, data reporting to various research organizations… more
- IQVIA (Durham, NC)
- …yields all the benefits of working for an industry leading global CRO and collaborating directly with cross-functional sponsor teams. Sponsor clients include world ... experts. + Author statistical analysis plans. + Monitor internal and CRO project activities including timelines, deliverables, and availability of resources. +… more
- Lilly (Boston, MA)
- …bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and ... technical and nonclinical study reports + Collaborate with external partners/ CRO to initiate new studies and occasionally travel to... to initiate new studies and occasionally travel to CRO to coordinate and monitor studies + Analyze, interpret,… more