- Locations: California, Massachusetts, Illinois, New York, New Jersey
- Related Keywords: Disclosure, Trial
- GAAP Accounting Manager
- Business Services Company (New York, NY)
- ...and procedures; provide analysis and support as required in SEC disclosure format. Become proficient in the use of our reporting...assigned accounts and maintain accurate accounting records, general ledger, and trial balance for US companies. Assist in providing monthly management...
- Manager, Contracts Administration
- Telecom Service Provider (Denver, CO)
- ...Officer and outside attorneys, including without limitation, vendor and service contracts, master agreements, consulting agreements, software trial agreements, software licensing & services agreements, customer agreements, supply agreements, confidentiality or non- disclosure ...
- Clinical Trial Registration and Results Disclosure Associate
- Takeda Pharmaceuticals (Deerfield, IL)
- ...deadlines. * Develops and updates registration and results disclosure processes as needed. * Develops and maintains the Clinical Trial Disclosure Master Log and other logs as needed. Provides logs of information to other functional areas eg Clinical Operations, Regulatory Affairs,...
- Clinical Trial Registration and Results Disclosure Associate
- Takeda Pharmaceuticals North America (Chicago, IL)
- ...of upcoming deadlines. Develops and updates registration and results disclosure processes as needed. Develops and maintains the Clinical Trial Disclosure Master Log and other logs as needed. Provides logs of information to other functional areas eg Clinical Operations, Regulatory...
- Clinical Trial Registration and Results Disclosure Associate
- Takeda Pharmaceuticals (Chicago, IL)
- ...deadlines. * Develops and updates registration and results disclosure processes as needed. * Develops and maintains the Clinical Trial Disclosure Master Log and other logs as needed. Provides logs of information to other functional areas eg Clinical Operations, Regulatory Affairs,...
- Clinical Trial Coordinator, Medical Affairs
- Biogen Idec (Wellesley, MA)
- ...audit-ready clinical trial documentation and study status in tracking tools .Manages and tracks regulatory/IRB/EC/REB documentation, Confidentiality Disclosure Agreements, and other clinical trial documents .Ensures necessary study supplies are available as per study timelines...
- Associate Senior Counsel (R&D:EMR & Morphotek support)
- Eisai (Ridgefield Park, NJ)
- ...FDA regulatory issues, GCPs, fraud and abuse/antikickback statues, subject injury, healthcare compliance, privacy (HIPAA) and clinical trial results disclosure laws and requirements preferred * Experience supporting R&D function preferred * Interface with in-house attorneys (in...
- Global Trial Manager III
- Vaktech (Chester, PA)
- HIJob Title: Global Trial Manager IIILocation: Chester brook, PAPay Rate: $ 65 / hrLength:02 YrsDescription:Responsible...and may contain confidential and/or privileged information. Any unauthorized review, use, disclosure or distribution is prohibited. If you do not wish to...
- Director
- Bristol Myers Squibb (Wallingford, CT)
- ...efficacy data and adherence to the protocol. Responsible for clinical study reports, protocol facing regulatory documents, and public disclosure of clinical trial results. Responsible for medical monitoring of clinical trial subjects. Designs and implements safety monitoring plans....
- Clinical Business Systems Manager
- LifeCell (Branchburg, NJ)
- ...clinical projects * Liaise with Legal Affairs and Corporate Compliance to develop, maintain and modify (as necessary) templates for clinical trial agreements, confidentiality agreements, financial disclosure statements, etc * Identify potential vendors to fill the needs of clinical...
- Clinical Trials Coordinator
- Biogen Idec (Boston, MA)
- ...audit-ready clinical trial documentation and study status in tracking tools oManages and tracks regulatory/IRB/EC/REB documentation, Confidentiality Disclosure Agreements, and other clinical trial documents oEnsures necessary study supplies are available as per study timelines...
- Clinical Trials Coordinator
- Biogen Idec (Wellesley, MA)
- ...audit-ready clinical trial documentation and study status in tracking tools yyyManages and tracks regulatory/IRB/EC/REB documentation, Confidentiality Disclosure Agreements, and other clinical trial documents yyyEnsures necessary study supplies are available as per study timelines...
- Clinical Trials Coordinator
- Biogen Idec (Wellesley, MA)
- ...audit-ready clinical trial documentation and study status in tracking tools yyyManages and tracks regulatory/IRB/EC/REB documentation, Confidentiality Disclosure Agreements, and other clinical trial documents yyyEnsures necessary study supplies are available as per study timelines...
- Contracts Administrator/Paralegal (temporary)
- FibroGen, Inc. (San Francisco, CA)
- ...working environment. This person will assist FibroGen attorneys and team members in the intake, drafting,and post-execution administration of non- disclosure , material transfer, clinical trial , vendor services, and other agreements. This individual must be highly-motivated and...