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Job Overview CRA I or II Southeast Experience Required, Non Oncology Why settle for one thing when you can have everything. Covance by labcorp gives you the best two for one opportunity for career growth. Who doesn't want twice the perks working at Covance one of the largest FSP CROs and partnering with one sponsor with a dedicated therapeutic focus. Dedicated to an FSP project you will bring your
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Job Overview Labcorp Drug Development, a global contract research organization, has worked on all of the top 50 best selling drugs available today through its full spectrum of nonclinical, clinical and commercialization services with our clients from leading pharma and agile biotech. Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of
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Job Overview SnapIoT's (a Covance/LabCorp company) platform, SnapClinical, is the industry's only self service mClinical platform that scales the development & deployment of patient centric mobile solutions. snapIoT relieves Sponsors and CROs from outdated eCOA/ePRO and technology enabled services providers that work inefficiently in unscalable, siloed models. Our platform deploys solutions up to
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Job Overview Senior Clinical Scientist Oncology Clinical Trial Mgmt and Medical Monitoring experience is required Remote in the USA or Canada Position leads Phase 1 3 Clinical Trials and oversees medical monitoring. This is not a laboratory/research scientist role. Why settle for one thing when you can have everything ? Covance by Labcorp gives you the best two for one opportunity for career growt
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Ensure that the Quality System is compliant with domestic and international quality system regulations (21 CFR 820; ISO 13485). Promote awareness of the Quality System and provide training to individuals across the organization on quality management principles, tools, techniques and best practices. Support the implementation of corporate policies and procedures relating to quality, design control,
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Job Overview The Vice President, Medical Affairs provides medical consultation for the entire Labcorp Drug Development Central Laboratory Services globally and the global Labcorp Drug Development CLS medical client base. The incumbent is responsible for medical decision making for the disciplines of the Laboratory. Additional responsibilities include consulting with Quality Assurance, Regulatory A
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Job Overview Depending on the scope of the project and experience level, job duties below may be performed independently as a Lead SUPM or in collaboration with a Lead SUPM as a Regional SUPM. Lead SUPM is accountable for all job duties below. Regional SUPM supports Lead SUPM by leading below job duties on a regional level. GENERAL Lead start up team during study start up phase liaising directly w
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Organizes and conducts routine and non routine sample analysis in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines. Documents work and maintains study documentation and laboratory records. Performs QC review of data. Sets up, operates and performs routine and non routine maintenance on general equipment. Provides input and participates in project meetings, plan
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Job Overview Responsible for line management / mentoring / coaching of the Modeling team including coordination and evaluation of the team Oversight of the team accountable for the development, analysis, interpretation and presentation of evidence based planning for implementation to deliver clinical trials Obtain and assess the relevant strategic/ operational data and additional information to de
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Job Overview We are seeking a Director Early Scientific Engagement to be based out of one of our Clinical sites. Duties will include the following Early Client Engagement (Specifics) Develops relationships with clients and broader drug development community to engage early to understand their upcoming portfolio needs and evolving expectations Leverages this market intelligence to advise on scienti
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Job Overview Labcorp Drug Development is seeking candidates for a Manager, Regulatory Submissions. The Manager, Regulatory Submissions will be remotely (home based) located anywhere within the United States or Canada. The Manager, Regulatory Submissions will be responsible for ensuring the timely submissions of appropriate documentation to Regulatory Authorities globally prior to the performance o
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Provide consultative and laboratory support both internally and to our clients. Oversee medical decision making and fulfill laboratory functions requiring a pathologist. Collaborate in global trials involving whole slide imaging and artificial intelligence platforms. Participate in the review and approval of new test offerings and service feasibilities. Review abnormal peripheral blood smears and
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Job Overview Prepare robust business planning through accurate budgeting/forecasting Lead business partner supporting two key business units of FSPx Assist the preparation of financial plans to understand the drivers of revenues and costs Conduct monthly variance analyses Identify & lead process improvement Dynamic business partner who leverages relationships to drive financial planning Work with
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Job Overview Labcorp Drug Development is seeking candidates for a QA Compliance Lead Auditor. The QA Compliance Lead Auditor will be remotely located (home based) anywhere within the United Sates. Conduct work as identified on the audit activity table (listing on table is not all inclusive but a representative sample) Takes lead in generation of global QA policies on interpretation/ application of
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Job Overview Labcorp Drug Development continues to grow! We currently have a great opportunity for an Associate Study Director to join our Preclinical Oncology team in Greenfield, IN. Our work in developing new pharmaceutical solutions has an incredible impact on millions of lives worldwide. Be a part of this life saving work. In this role, you will learn to serve as a Study Director. Some of the
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