management, particularly in the oncology field. Requirements: Bachelor's degree in Life Sciences, Computer Science...
performed. All other duties as assigned. Requirements: Bachelor's degree from an accredited institution with a major in Life... Sciences, Computer Science, or relevant field of study; or equivalent practical experience. 6+ years of Clinical Data...
's degree in Life Sciences, Computer Science, or a related field. Minimum of 3 years of clinical data management experience...
. Strong understanding of medical device product life cycle and regulatory requirements. In-depth knowledge of ISO 13485, FDA regulations...
Responsibilities: Prepares robust regulatory applications (either for FDA or for international regulatory agencies) to achieve departmental and organizational objectives. Creates, reviews, and approves engineering changes. Acts as core ...
Responsibilities: Ensure departmental or functional training plans in place and appropriate. Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time del...
Responsibilities: Leads, performs, and oversees data management activities for clinical studies and/or clinical programs. Performs hands-on clinical data management tasks to support clinical studies, including, but not limited to reviewi...
Responsibilities: The Regulatory Coordinator is responsible for the coordination, preparation, and maintenance of regulatory documentation and compliance for clinical trials. This role ensures adherence to local, state, and federal regul...