A Senior Clinical Study Manager is available in Princeton, NJ courtesy of Adecco Medical & Science. This is a contract-to-hire opportunity that requires some travel (25% in the U.S.). This professional will role up their sleeves and do the work. They will be responsible for the overall management for phases I - III of the clinical studies. This person will ensure the day-to-day operations in support of global clinical research initiatives. This person will be responsible for the consistency, quality and performance against the study plan. This person will also be skilled in peer and CRO management. A clinical trials leader who is a real diplomat and project manager in the pharmaceutical industry. The pay rate is open. This person MUST:
Know how to run studies
Have strong experience with phases I-III
Clinical Data Management
Case Report Forms
Patient Recruitment Strategies
CRO relationship management
Study Financial Management
Management of the trial contracts
2-5 years of clinical trial management experience
3-5 years of clinical operations experience
B.S. degree in the biological sciences
Strong understanding of medical terminology
Knowledge of FDA/GCP/ICH, regulations, etc.
To be considered for the Sr.Clinical Study Manager, please use the "apply now" button to submit your resume.
If you have questions about the position please contact Heena Verma at 212.497.5751 or at email@example.com.
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