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... two are described here: The Specialist/Manager Regulatory Operations contributes to the strategic ... strategic planning and preparation of regulatory submissions and supports the formatting, ... organization, and structuring of..
... Myers Squibb Clinical Trial Result Specialist in Princeton New Jersey Bristol-Myers ... The Clinical Trial Results Reporting Specialist is responsible for creation of ... the databases. The Results Reporting..
Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas ..
... software development oversight to assure regulatory compliance across the end-to-end product lifecycle ... etc. Ensure adequate and timely regulatory compliance support Report on key metrics ... tower Provide active..
At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and ..
Overview To be part of our organization, every employee should understand and share in the YNHHS Vision, support our Mission, and live our Values. These values - integrity, patient-centered, respect, accountability, ..
... The Quality E- Systems Senior Specialist’s primary responsibility is to help ... assure the quality, integrity, and compliance of site Information Technology (IT) ... functional areas. Altogether, the Senior..
PHARMACIST - REVENUE INTEGRITY PROGRAM','PHA006S2','!*! Position: Pharmacist / Revenue Integrity ProgramLocation: Lenovo Building / MorrisvilleHours: Full Time, 32 hrs/wk; DaysPosition Summary: The Revenue Integrity pharmacist will join the Pharmacy Revenue Integrity ..
... for clarification or revision Assures regulatory guidelines are followed for electronic ... ready documents and dossiers for compliance to these guidelines. Demonstrates a ... Demonstrates a working knowledge of..
... Research and Development / Global Regulatory, Safety and Biometrics / Global ... and Biometrics / Global Submissions Regulatory Policy - Global Regulatory Business Capabilities Functional Area Description ... Capabilities..
... business results. Clinical Supply Operations Specialist will lead the manufacture of ... ensuring strict adherence to applicable regulatory, safety, and company policies and ... policies and procedures. In addition,..
... Marketing, Sales Operations, Medical, Legal, Compliance, etc.) to appropriately address business ... aids, etc.) that meet all regulatory, legal and compliance requirements for assigned individual projects ... Operations, Commercial..
... Practice (GCP), and the applicable regulatory requirement(s). Act as one of ... analysis are implemented Involvement in Regulatory Compliance audit/inspection process, as needed. This ... Vendor Operations Managers, Regional..
... business results. Training & Development Specialist The Training & Development Specialist is responsible for the successful ... site Manufacturing Training Program. The Specialist assists in determining training solutions .....
... consistency, quality of work and compliance with external regulations and internal ... users and internal Global Quality compliance staff to ensure that CSV ... technology solutions that improve digitization,..
... Global Clinical Trial-Submission Unit (GCT-SU) Specialist: This role has two key ... 1) Provide support to Senior specialist in CTAp preparation activities 2) ... trial application activities are in..
... SCOPE OF POSITION: The Senior Specialist is responsible for providing quality ... associated reports and procedures. Ensure compliance with the site validation master ... is compliant with global and..