Job Description
**POSITION SUMMARY**
You will be responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within our Oncology portfolio.
**KEY RESPONSIBILITIES**
+ Clinical development expert for assigned studies maintaining current scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment.
+ Effectively partner with other clinical and medical colleagues, clinical operations and other functional lines for the successful implementation and execution of the clinical trial(s) within the assigned program.
+ Responsible for scientific oversight, data integrity and quality of the clinical trial(s).
+ Represent the study team in governance meetings and submissions, partners with/supports the Development lead/Medical Director regarding study and disease area strategy.
+ Author protocols, study level informed consent documents, and contributes to authorin...
You will be responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within our Oncology portfolio.
**KEY RESPONSIBILITIES**
+ Clinical development expert for assigned studies maintaining current scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment.
+ Effectively partner with other clinical and medical colleagues, clinical operations and other functional lines for the successful implementation and execution of the clinical trial(s) within the assigned program.
+ Responsible for scientific oversight, data integrity and quality of the clinical trial(s).
+ Represent the study team in governance meetings and submissions, partners with/supports the Development lead/Medical Director regarding study and disease area strategy.
+ Author protocols, study level informed consent documents, and contributes to authorin...