A company is looking for a Regulatory Affairs Senior Associate to support regulatory document management and clinical trial submissions.
Key ResponsibilitiesMaintain regulatory document management and tracking systemsSupport activities for clinical trial and marketing application submissions and health authority correspondenceCollaborate with external partners and manage submissions related to protocol amendments and investigator updatesQualifications & Requirements1-2 years of regulatory experienceExperience with SharePoint, Excel, Smartsheet, and Veeva VaultAbility to work independently and manage multiple prioritiesExperience in providing training and support to team membersFamiliarity with compliance to SOPs and regulatory authorities
Senior Associate, Regulatory Affairs
In addition, Senior Regulatory Affairs Associate is responsible for supporting a variety of activities in the department related to regulatory submissions and R&D requests, and supporting other departments within the organization. Ability to review regulatory and scientific submission documents for ...
Regulatory Affairs Senior Associate
A company is looking for a Regulatory Affairs Senior Associate to support regulatory document management and clinical trial submissions. ...
Senior Associate, Regulatory Affairs - Sun Pharmaceutical Industries, Inc.
In addition, Senior Regulatory Affairs Associate is responsible for supporting a variety of activities in the department related to regulatory submissions and R&D requests, and supporting other departments within the organization. Ability to review regulatory and scientific submission documents for ...
Senior Associate, Regulatory Affairs
In addition, Senior Regulatory Affairs Associate is responsible for supporting a variety of activities in the department related to regulatory submissions and R&D requests, and supporting other departments within the organization. Ability to review regulatory and scientific submission documents ...
Senior Associate, Regulatory Affairs
In addition, Senior Regulatory Affairs Associate is responsible for supporting a variety of activities in the department related to regulatory submissions and R&D requests, and supporting other departments within the organization. Ability to review regulatory and scientific submission documents for ...
Senior Analyst Regulatory Affairs
A company is looking for a Senior Analyst, Regulatory Affairs to join their Corporate Counsel team. ...
Associate Director, Regulatory Affairs Strategy - Genetic Medicine
The Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. Utilize regulatory expertise and knowledge...
Associate Director Regulatory Affairs
A company is looking for an Associate Director, Regulatory Affairs and Submissions. ...
Senior Specialist, CMC Regulatory Affairs
CMC Regulatory Affairs Specialist performs regulatory assessment of changes. Interpreting the current, approved and planned clinical regulatory landscape by contributing to the regulatory submission form process. Reviews regulatory submissions to ensure all aspects of global regulatory and CMC compl...
Regulatory Affairs Associate
The Regulatory Associate will report to the Senior Manager, Regulatory Affairs and, under the direction and guidance of the Associate Vice President, will help to ensure regulatory compliance of Prestige marketed products. Assist with regulatory affairs projects and initiatives as needed, including ...