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At the forefront of what we do is the potentially positive impact our efforts can have on improving the lives of critically ill patients. Our dedicated and talented clinical development and management teams are among the best in the industry, with long track records of successfully developing novel therapeutics. We strive to foster a collaborative, creative, and science-driven environment where our employees can take pride in their accomplishments and where their contributions are valued.
We’re centered on our five core corporate values, and we look for potential employees who embody the same ideals.
Our Core Values
- We put patients first
- We solve problems with urgency
- lives depend on our creativity, persistence, and optimism
- We do what we say we’ll do – no matter how small the commitment
- We are curious and constantly learning
- good ideas can come from anyone, so we listen with sincerity and humility
- We are honest about where the data lead us
- We are candid in all our communications
- transparency builds trust and leads to quality
- We ensure our contribution is not defined by our job description
- We pursue diversity in all forms because it makes us better
- We do what’s right - even when no one is watching
- We are kind and respectful
- these are cornerstones of strength – not weakness
- We invest wisely
- focus and efficiency impact the value we can create for patients
Chimerix, Inc. is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class. Consistent with our commitment to equal employment opportunity, Chimerix provides reasonable accommodations to qualified individuals with disabilities who need assistance in applying electronically for a position, unless doing so would impose an undue hardship. To request a reasonable accommodation for this purpose, please send an email to hr@chimerix.com or call 919-806-1074.
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The Associate Director of Quality Systems will be responsible for providing technical expertise, specifications, documentation, validation, and training on the company's Quality activities. This position will report to the Executive Director, Quality Assurance
Primary Responsibilities:
- Ensure the Implement and maintenance of QA-GXP systems and activities
- Generate and review of documents used in GXP applications.
- Manage the process for development and maintenance of GXP SOPs
- Conduct GXP audits
- Lead GXP investigations and perform root cause analyses. Provide critical analysis of the implications and proposed resolutions to potential GXP quality...
DIRECTOR, BIOSTATISTICS
Department: Clinical Development
Schedule: Full Time
Location Note: This position may be located remotely or in Durham, North Carolina.
The successful candidate will provide statistical input into all aspects of clinical trials, from design through statistical analysis and reporting. Deliver statistical support for regulatory interactions and submissions. Work within teams and interact closely with Medical, Clinical Operations, Data Management, Clinical Pharmacology, Pharmacokinetics, Bioanalytical, Regulatory Affairs,...
DIRECTOR, COMMERCIAL FP&A:
The Commercial Financial Planning & Analysis (FP&A) Director will serve as a key member of the finance & accounting team and reports to the Chimerix Chief Financial Officer. This leadership position plays a significant role in Financial Planning & Analysis, revenue recognition, process development, capital management and financial reporting.
Director, Regulatory Affairs, Advertising and Promotions
As the Director, Regulatory Affairs, Advertising and Promotions at Chimerix, you will be integral to the development, review, risk assessment and approval of all advertising and promotional materials. Your role encompasses supporting and managing regulatory aspects of the review system, working cross functionally to drive efficient and compliant promotional material development, review and approval. You will also be the regulatory lead for all materials submitted to regulatory agencies, especially US FDA, for notification and/or review. This role requires effective leadership, communication, problem-solving, critical thinking skills and maintenance of...
RESEARCH SCIENTIST:
Responsible for the design, execution and interpretation of molecular profiling (e.g. NGS) nonclinical and clinical studies that evaluate mechanism of action pharmacology and efficacy of novel cancer therapies. Design and implement molecular profiling analyses, in addition to pharmacology studies that are conducted in-house.