Clinical Study Manager Job in East Hanover, New Jersey Us

Confidential Posting

About the Job

Job Description

Ensure all trial deliverables are met according to timelines, budget, operational procedures and quality standards
Manage interactions with Global Clinical Development Operations, Drug Supply Management and other relevant functions
Manage contract Research Organizations
Support the development, management and tracking of trial budget
Responsibility for accuracy of trial information in all clinical databases and tracking systems
Contribute to ongoing scientific review of the clinical data and support trial data analysis
Manage/answer questions related to trial procedures and patient eligibility
Responsibility for implementation of best practices and standards for trial management within the therapeutic area

Qualifications/experience

Study start-up experience required
Demonstrated capabilities in supporting trial planning and execution
Good communications skills
Proven ability to work both independently or in a team setting and to meet set goals by managing own timelines
Knowledge of good clinical practice; clinical trial design; understanding of overall drug development process
Minimum of 3 years clinical trial management experience
Bachelor's degree in life science/healthcare