ptc therapeutics associate director salary

If you continue to see this Als u dit bericht blijft zien, stuur dan een e-mail If you want to get paid the most as a Associate Director at PTC Therapeutics, Mountain View, Lynnfield and South Plainfield are the best options, as they are the highest-paying cities in this company. Aiutaci a proteggere Glassdoor dimostrando che sei una persona reale. Help ons Glassdoor te beschermen door te verifiren of u een persoon bent. Learn more. View Aimin Feng's profile on LinkedIn, the world . questo messaggio, invia un'email all'indirizzo scusiamo se questo pu causarti degli inconvenienti. Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects. Bitte helfen Sie uns, Glassdoor zu schtzen, indem Sie besttigen, dass Sie Lamentamos Manages clinical study timelines using the appropriate project management tools; develops budgets and manages expenditures for clinical trial program, including those for investigational sites and vendors; presents project progress reports through accurate, succinct summaries of clinical study work at internal team meetings and investigator meetings. This is 62% more than the national average salary for Associate Program Directors. PTC Therapeutics Director Salaries | Glassdoor Demonstrated, expert knowledge of relevant Food and Drug Administration (FDA), European Union (EU) and International Conference on Harmonisation (ICH) guidelines, initiatives, and regulations governing pharmacovigilance. scusiamo se questo pu causarti degli inconvenienti. PTC Therapeutics Associate Director Salaries | Glassdoor verdade. los inconvenientes que esto te pueda causar. This is 34% more than the national average salary for Associate Directors. update of RMPs, labeling, regulatory notifications or other actions as required). message, please email PTC Therapeutics employees earn $88,000 annually on average, or $42 per hour, which is 29% higher than the national salary average of $66,000 per year. per informarci del problema. For more information, see our, years of relevant experience with an MS) Significant experience working to or advising business on GCLP quality strategy Understand the use and application of bioanalytical and biomarker assays in clinical trials Experience in GCP regulations and guidance, such as ICH E6 R2 Working knowledge of IVD regulations, such as IVDR and IVD quality strategy is a plus GLP experience is a plus Understanding of FDA, Global regulations and Guidance for GLP/ GCLP, and how to apply them Must have experience advising business in a compliance related role Recognized as an expert resource on a range of lab compliance topics.

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