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We are currently seeking an Associate Director, Clinical QA to assist in the development and oversight of a total quality system. The primary responsibilities of this position will be CRO Qualification/Auditing, PI GCP auditing, and Sponsor Clinical QA. Requirements: ? Direct1/11/2015 Durham, NC Save This Job
The Senior IT Manager will plan, coordinate and design all IT-related activities to ensure the streamlined operation of the IT Department in alignment with the business objectives of the organization, as well as defining and implementing IT policies, procedures and best1/11/2015 Durham, NC Save This Job
We are currently seeking an Medical Science Liaison who will develop professional relationships with thought leaders and academic centers. The successful candidate will translate those relationships into research opportunities and provide timely, accurate product information to1/11/2015 Durham, NC Save This Job
We are currently seeking an experienced Executive Assistant to serve as the right hand for a senior executive in our organization. This position will be responsible for scheduling, providing appointment updates, gathering information, filing, preparing slides, and/or meeting1/11/2015 Durham, NC Save This Job
Based out of London, the Director, Medical Affairs- EU will develop and execute a Medical Affairs strategy for products consistent with scientific and commercial goals throughout Europe. Drives elements crucial for regulatory and commercial success. Participates in scientific1/11/2015 Durham, NC Save This Job
We are currently seeking a Director, Project Management to provide leadership and program management support to cross-functional development project. The successful candidate will liaise with internal management team, functional leaders and external partners championing a1/11/2015 Durham, NC Save This Job
We are currently seeking an Associate Director, GMP/ Quality Control to assist in the development and oversight of a total quality system. The primary responsibilities of this position will be Vendor Qualification/Auditing, GMP verification, and Quality1/11/2015 Durham, NC Save This Job
Responsible for all aspects of one or more global clinical trials from the preparation, execution, and reporting associated with clinical trials in accordance with GCP/ICH guidelines and local/country regulatory requirements. Facilitation and coordination and full project1/11/2015 Durham, NC Save This Job
We are seeking a Drug Manufacturing Manager to join our Research and Development team. This individual will report directly to our AD, Pharmaceutical Development and will focus primarily on oversight of CDMO/CMOs. Responsibilities: - Design evaluate, validate, and oversee1/11/2015 Durham, NC Save This Job
Develop and execute a Medical Affairs strategy for products consistent with scientific and commercial goals. Direct and oversee all activities related to the Medial Affairs function. Works with key stakeholders in protocol design and in determining study elements crucial for1/11/2015 Durham, NC Save This Job
We are seeking an experienced Medical Director to provide medical and scientific input for all medical aspects of a set of clinical development programs. The selected individual will be responsible for providing correct and updated scientific and medical information for the1/11/2015 Durham, NC Save This Job
We are currently seeking a AD/Director, Preclinical Development to be responsible for preclinical ADME and toxicology studies conducted by or on behalf of Chimerix. The selected individual will be responsible for the communication of studies orally and in writing to company1/11/2015 Durham, NC Save This Job