, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business operations, and emerging issues..., regulatory submissions and responses, and other program documents. · May serve on a Integrated Evidence Strategy Team as the...
, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues..., regulatory submissions and responses, and other program documents. · May serve on a Integrated Evidence Strategy Team as the...
Affairs, and Regulatory Affairs teams. Advise on a broad range of matters involving the Food and Drug Administration (FDA.... Clinical R&D Legal Academy Work on a wide range of clinical-trial related legal and regulatory matters in support of AbbVie...
Affairs, and Regulatory Affairs teams. Advise on a broad range of matters involving the Food and Drug Administration (FDA.... Clinical R&D Legal Academy Work on a wide range of clinical-trial related legal and regulatory matters in support of AbbVie...
programs; for generating scientific evidence to support medical affairs strategies; and for interacting with regulatory... on , , , , and . Job Description **This is a hybrid on-site position. Candidates must be local to Lake County, IL or Florham Park, NJ Medical Affairs & Health...
programs; for generating scientific evidence to support medical affairs strategies; and for interacting with regulatory... on , , , , and . Job Description **This is a hybrid on-site position. Candidates must be local to Lake County, IL or Florham Park, NJ Medical Affairs & Health...
- functional colleagues who support clinical trial execution and the Development and Global Medical Affairs Therapeutic Area MDs... operations content to clinical and regulatory documents (e.g., INDs, IB, NDAs, BLAs, MAA, Regulatory Briefing Books) Responsible...
- functional colleagues who support clinical trial execution and the Development and Global Medical Affairs Therapeutic Area MDs... operations content to clinical and regulatory documents (e.g., INDs, IB, NDAs, BLAs, MAA, Regulatory Briefing Books) Responsible...
, and cost-effective products for treatment of vascular disease. As the Specialist in Global Clinical Affairs, considered... for reports submitted to the regulatory agencies. Monitors adherence to protocols and determines study completion...
affairs. Study Management Associate Organization: The Study Management Associate Organization (SMAO) is responsible... teams, including but not limited to data management, regulatory affairs, Clinical Site Management (CSM) and external...
affairs. Study Management Associate Organization: The Study Management Associate Organization (SMAO) is responsible... teams, including but not limited to data management, regulatory affairs, Clinical Site Management (CSM) and external...
to regulatory and internal standards. Collaborate with business stakeholders, Legal, Medical Affairs, R&D, and external consultants... effectively in fast-paced environments. Qualifications - Associate degree required; Bachelor's degree preferred. 3 5 years...
, Clinical Study Reports, regulatory submissions and responses, and other program documents. May oversee the work of Associate... on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business...
, Clinical Study Reports, regulatory submissions and responses, and other program documents. May oversee the work of Associate... on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business...
, Clinical Study Reports, regulatory submissions and responses, and other program documents. May oversee the work of Associate... on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business...
, Clinical Study Reports, regulatory submissions and responses, and other program documents. May oversee the work of Associate... on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business...
, Clinical Study Reports, regulatory submissions and responses, and other program documents. May oversee the work of Associate... on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business...
management, and regulatory affairs. Study Management Associate Organization: The Study Management Associate Organization... closely with cross functional teams, including but not limited to data management, regulatory affairs, Clinical Site...