Please note that the requirements specified in this posting are the basic qualifications required for the Pharmacovigilance Scientist position; however, job title will be dependent on the candidate's level of experience in those...

Please note that the requirements specified in this posting are the basic qualifications required for the Medical Writer position; however, job title will be dependent on the candidate's level of experience in those requirements.OBJECTIVE:Executes...

OBJECTIVE:The Medical Director is responsible for the development and implementation of the medical and scientific communication platform, research strategies including post-approval investigator initiated research, phase 4 and contracted research. ...

OBJECTIVES:Responsible for ensuring ongoing review and agreement of the Therapy Area Strategy and associated documents formulated by the TA leader prior to their review and approval by appropriate governance committees. Oversees the development and...

OBJECTIVES:* Manage TGRD Clinical Compound Support Program Managers. Ensure that investigator, vendor, facility and system audits are conducted, and communicate any critical compliance risks noted from these activities to Quality Assurance senior...

Please note that the requirements specified in this posting are the basic qualifications required for the Medical Director position; however, job title will be dependent on the candidate's level of experience in those requirements.OBJECTIVES:The...

OBJECTIVE:This position is responsible for oversight of activities, timelines, and cross functional coordination for documents coming from PV, including regulatory submissions and responses, aggregate reports, white papers, etc. The position is also...

OBJECTIVE:The purpose of this position is to manage Takeda's compliance with Federal and State transparency requirements as well as other ancillary areas such as restrictions on interactions with Health Care Practitioners (HCPs) or Health Care...

OBJECTIVES:The purpose of this position is to ensure that TGRD clinical trial activities for all assigned projects are conducted in compliance with applicable regulations, Good Clinical Practice (GCP) guidelines, the International Conference on...

OBJECTIVES:* Oversees as well as executed all regulatory activities of multiple projects including one highly complex project for assigned marketed product(s) of responsibility.* Manages director reports to support scope of project work.* Provides a...