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[J-968] - ASSOCIATE, IP LITIGATION (HATCH WAXMAN ACT)

Associate, ip litigation (hatch waxman act) orrick is seeking associates with over 2 years of experience to join our intellectual property group, focusing on hatch waxman litigation and related regulatory matters. the candidate will have a strong background in pharmaceutical patent law and a deep understanding of the hatch waxman act. the position can be based in our new york or los angeles offices. we are seeking candidates who demonstrate strong academic performance, substantial experience in a law firm setting, and excellent writing and communication abilities. preference will be given to those with technical degrees in chemistry, biology, or related fields. the ideal candidates will have over 2 years of experience specifically in hatch waxman litigation. candidates should have experience in drafting briefs and engaging in all phases of fact and expert discovery. the most innovative companies in the world call on us to protect their intellectual property and defend their brands. we’ve won some of the highest-impact ip cases of recent years at trial and on appeal. with multiple experienced first-chair trial lawyers covering the full spectrum of patent, copyright, trademark, and trade secret disciplines, clients count on orrick to effectively handle any dispute from their most strategic and sophisticated problems to routine npe defense. qualifications: - excellent legal research, writing, and communication skills, highly organized with strong attention to detail. - ability to manage multiple projects and work effectively in a team environment. - background in lif...


CTA - PAYMENTS - [N-941]

Overview as a cta you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of the worlds premier biopharmaceutical companies. working across a vast portfolio of medicines and vaccines this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally. responsibilities what you will be doing: cta assists in the coordination and administration of the study activities from the start up to execution and close out, and within the local study team to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives - collects, assists in preparation, reviews and tracks documents for the application process as well as coordination and tracking of study materials and equipment - assist in submission of proper application/documents to ec/irb and, where appropriate to regulatory authorities - interfaces with investigators, external service providers and cras during the document collection process - local administrative main contact and works closely with the cras and/or the lsad for the duration of the study - set-up and maintenance of the local etmf and isf including document tracking in accordance with ich-gcp and local requirements - ensures essential documents are uploaded in a timely manner to maintain the etmf “inspection readiness” and study documents are ready for final archiving and completion of local part of the etmf and supports the cra in the close out ...


ASSOCIATE, IP LITIGATION (HATCH WAXMAN ACT)

Associate, ip litigation (hatch waxman act) orrick is seeking associates with over 2 years of experience to join our intellectual property group, focusing on hatch waxman litigation and related regulatory matters. the candidate will have a strong background in pharmaceutical patent law and a deep understanding of the hatch waxman act. the position can be based in our new york or los angeles offices. we are seeking candidates who demonstrate strong academic performance, substantial experience in a law firm setting, and excellent writing and communication abilities. preference will be given to those with technical degrees in chemistry, biology, or related fields. the ideal candidates will have over 2 years of experience specifically in hatch waxman litigation. candidates should have experience in drafting briefs and engaging in all phases of fact and expert discovery. the most innovative companies in the world call on us to protect their intellectual property and defend their brands. we’ve won some of the highest-impact ip cases of recent years at trial and on appeal. with multiple experienced first-chair trial lawyers covering the full spectrum of patent, copyright, trademark, and trade secret disciplines, clients count on orrick to effectively handle any dispute from their most strategic and sophisticated problems to routine npe defense. qualifications: excellent legal research, writing, and communication skills, highly organized with strong attention to detail. ability to manage multiple projects and work effectively in a team environment. background in life sciences or re...


CTA - PAYMENTS

Overview as a cta you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of the worlds premier biopharmaceutical companies. working across a vast portfolio of medicines and vaccines this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally. responsibilities what you will be doing: cta assists in the coordination and administration of the study activities from the start up to execution and close out, and within the local study team to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives collects, assists in preparation, reviews and tracks documents for the application process as well as coordination and tracking of study materials and equipment assist in submission of proper application/documents to ec/irb and, where appropriate to regulatory authorities interfaces with investigators, external service providers and cras during the document collection process local administrative main contact and works closely with the cras and/or the lsad for the duration of the study set-up and maintenance of the local etmf and isf including document tracking in accordance with ich-gcp and local requirements ensures essential documents are uploaded in a timely manner to maintain the etmf “inspection readiness” and study documents are ready for final archiving and completion of local part of the etmf and supports the cra in the close out activities for the isf prepar...


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