Responsibilities: Support clinical trial applications submitted via Clinical Trial Information System (CTIS... with other Trial Disclosure staff. Requirements: Bachelor's degree required, preferably in a health or biological science field. 1...
Responsibilities: Support clinical trial applications submitted via Clinical Trial Information System (CTIS... trains with other Trial Disclosure staff. Requirements: Bachelor's degree required, preferably in a health or biological...
Clinical Trial Operations (CTO) Internship Program at AbbVie. Clinical Trials are required before a new compound can... with activities associated with the development and implementation of strategic initiatives related to clinical trial initiation...
Clinical Trial Operations (CTO) Internship Program at AbbVie. Clinical Trials are required before a new compound can... with activities associated with the development and implementation of strategic initiatives related to clinical trial initiation...
successful global registration and commercialization of drug development projects. As a member of AbbVie's Clinical Trial Operations... on , , , , and . Job Description Clinical Trials are required before a new compound can be available for use by patients. A clinical study in human volunteers...
on , , , , and . Job Description The Clinical Process Compliance Associate is an independent contributor who assists the Quality Control, Compliance..., and/or Metrics team with the oversight of clinical trial activities based on the standards required to ensure adherence to GCP...
on , , , , and . Job Description The Clinical Process Compliance Associate is an independent contributor who assists the Quality Control, Compliance..., and/or Metrics team with the oversight of clinical trial activities based on the standards required to ensure adherence to GCP...
on , , , , and . Job Description The Clinical Process Compliance Associate is an independent contributor who assists the Quality Control, Compliance..., and/or Metrics team with the oversight of clinical trial activities based on the standards required to ensure adherence to GCP...
in a cross-functional setting. · Clinical trial experience in the pharmaceutical industry, academia, or equivalent is preferred.... · Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the...
electronic document conventions and processes consistently and accurately. Integrate clinical trial data across studies... to clinical trials and; to keep multiple reports moving forward simultaneously through multi-tasking. Responsibilities Prepare...
in a cross-functional setting. · Clinical trial experience in the pharmaceutical industry, academia, or equivalent is preferred.... · Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the...
electronic document conventions and processes consistently and accurately. Integrate clinical trial data across studies... to clinical trials and; to keep multiple reports moving forward simultaneously through multi-tasking. Responsibilities Prepare...
- functional colleagues who support clinical trial execution and the Development and Global Medical Affairs Therapeutic Area MDs.... An Associate’s degree/R.N. or equivalent with relevant experience is acceptable. Must have 12+ years of Pharma-related/ clinical...
- functional colleagues who support clinical trial execution and the Development and Global Medical Affairs Therapeutic Area MDs.... An Associate's degree/R.N. or equivalent with relevant experience is acceptable. Must have 12+ years of Pharma-related/ clinical...
, Clinical Study Reports, regulatory submissions and responses, and other program documents. May oversee the work of Associate... is desirable. At least 2 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent. Ability...
, Clinical Study Reports, regulatory submissions and responses, and other program documents. May oversee the work of Associate... is desirable. At least 2 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent. Ability...
, Clinical Study Reports, regulatory submissions and responses, and other program documents. May oversee the work of Associate... of a subspecialty fellowship is desirable. At least 2 years of clinical trial experience in the pharmaceutical industry, academia...
, Clinical Study Reports, regulatory submissions and responses, and other program documents. May oversee the work of Associate... of a subspecialty fellowship is desirable. At least 2 years of clinical trial experience in the pharmaceutical industry, academia...
, Clinical Study Reports, regulatory submissions and responses, and other program documents. May oversee the work of Associate... is desirable. At least 2 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent. Ability...
, trial design, evidence package evaluation, clinical acceleration, commercial presentation). Drive end-to-end strategic... success of AbbVie. As Associate Director, Innovation, you will partner with leaders across AbbVie to optimize the value...