- Takeda Pharmaceuticals (Boston, MA)
- …based in Cambridge, MA reporting to the Head Partnership Health and Supplier Management . At Takeda, we are transforming the pharmaceutical industry through our ... of portfolio, through cross-functional collaboration, proactive risk and issue management and utilizing data-driven analytics. **_ACCOUNTABILITIES:_** + Lead and… more
- US Tech Solutions (IL)
- …activities; involvement with the transfer of TMFs from external entities (ie, CRO , other pharmaceutical companies).** + Review regulatory documents / packages ... other TMF stakeholders (ie, CPD, SM&M, DSS, BSO).** **For CRO managed study TMFs: conduct QC of artifacts (may...eTMF system navigation, including being present in the front room with the Auditors/Inspectors - participate in responding to… more
- Charles River Laboratories (Wayne, PA)
- …and serves as a member of the Regulatory Affairs and Compliance management team. Provides direction in implementing the Charles River Compliance Program and ... and corporate policies. ⦁ Maintain a close working relationship with site/operation management to assure a cohesive approach to regulatory compliance. ⦁ Assure staff… more
- Charles River Laboratories (Wilmington, MA)
- …with technical leads and site schedulers. * Partner with operations/technical management to prioritize ongoing work to manage and meet competing project ... work, for cost and billing purposes. * Manage and control project scope, timelines, and budget, and when appropriate,...assist with scope and pricing reviews. * Utilize project management software that allows timely and open communication of… more
- Charles River Laboratories (Ashland, OH)
- …nonclinical research studies of basic to moderate complexity, to include study management , interpretation and reporting of study data, and assuring the regulatory ... as they apply to the conduct of nonclinical research. * Participate in proposal management and bid development process. Assist in the review of Letters of Commitment… more
- IQVIA (Durham, NC)
- …you get all the benefits of working for an industry leading global CRO while collaborating with sponsor teams and utilizing sponsor systems. These sponsor clients ... include world class pharmaceutical and biotech companies offering you unique opportunities to...and external experts. + Review eCRF and other data management documents. + Create or review randomizations and related… more
- United Therapeutics (Research Triangle Park, NC)
- …+ 5+ years of project management experience in clinical operations management , overseeing clinical trials in pharmaceutical environment or related experience ... and other relevant functional groups (UT and / or CRO ) to manage and engage with clinical study sites,...or + 5+ years of related project management experience in clinical research/ pharmaceutical industry +… more
- Sumitomo Pharma (San Francisco, CA)
- Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... an experienced Sourcing/Procurement manager to deliver strategic sourcing, contract management , supplier market intelligence, financial productivity, supplier performance … 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 ... class pharmaceutical and biotech companies offering you unique opportunities to...+ Author statistical analysis plans. + Monitor internal and CRO project activities including timelines, deliverables, and availability of… more
- Charles River Laboratories (Reno, NV)
- …and perform record keeping. * Review data recorded by others for quality control . * May record observations and measurements for basic lab/research tasks * Perform ... About Charles River Charles River is an early-stage contract research organization ( CRO ). We have built upon our foundation of laboratory animal medicine and… more