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CymaBay is a clinical stage biopharmaceutical company focused on developing and providing access to innovative therapies for patients with liver and other chronic diseases. If you are ready to join a team where your work is challenging, rewarding and meaningful; where your efforts are recognized and appreciated; where your career and skills are developed and expanded; AND where you are truly VALUED… then CymaBay is looking for YOU!. Position Summary:. As an Associate Director of Clinical Operations (AD Clin Ops) you will be accountable for leading, or providing oversight of, multiple studies t... view job details
At CymaBay, we are a clinical stage biopharmaceutical company committed to improving the lives of patients with liver and other chronic diseases by developing and providing access to innovative therapies. We are dedicated to enhancing the quality of healthcare by addressing the complex needs of patients, caregivers and communities and advancing medical knowledge.. CymaBay is expanding to support the re-initiation of clinical programs! We are looking for new team members to join and who support our mission.. Position Summary:. As an in-house Clinical Research Associate (CRA) you will work close... view job details
At CymaBay, we are a clinical stage biopharmaceutical company committed to improving the lives of patients with liver and other chronic diseases by developing and providing access to innovative therapies. We are dedicated to enhancing the quality of healthcare by addressing the complex needs of patients, caregivers and communities and advancing medical knowledge.. CymaBay is expanding to support the re-initiation of clinical programs! We are looking for new team members to join and who support our mission.. Position Summary:. As a Clinical Trial Manager (CTM) you will be in charge of driving s... view job details
Position Summary:. Oversee quality operations associated with CymaBay's Clinical Programs and ensuring quality compliance at contract manufacturing compliance organization (CMO) sites. Responsibilities include, but are not limited to, coordinating resolution of quality related issues, review of change controls, QA lot disposition, compilation of trending reports, and assisting with quality investigations and product complaint investigations to ensure compliance with applicable regulations and regulatory commitments. This includes the quality oversight of contract vendors, and lot disposition t... view job details
Summary:. The Regulatory Operations Specialist will report to the senior manager regulatory operations and provide support for the regulatory department to ensure efficient and compliant business processes associated with regulatory submissions.. Essential Functions and Job Responsibilities:. Formatting, publishing and assembly of regulatory submissions in support of INDs and NDAs. Conduct proofreading and quality checks of regulatory documents and submissions. Prepare and route for review and signature, regulatory correspondence and draft submissions. Collaborate with Regulatory Strategists i... view job details
Participate in weekly strategy discussions of forecasted opportunities. Delivery a territory management plan that outlines within a specific territory. Utilize company provided tools to achieve sales success and prepare documents according to established company guidelines. view job details
Assist residents with move-in. Utilizes several trade skills such. Responds to emergency situations during and after regular work hours, i. view job details
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Managed an entire product lifecycle from concept to release. Contribute to the development of the creative teamÆs culture and quality standards. delivering, and tuning online multi-platform experiences (web, mobile, tablets). view job details
There is currently no job description for Scientist I - Biotech. Be the first to submit the job responsibilities for a Scientist I - Biotech.