Sr. Clinical Data Associate Endocyte

The Senior Clinical Data Associate supervises data management activities at the clinical trial level and ensures that all data management-related study objectives and timelines are met.

Responsibilities:

Reviews clinical protocols and determines data management requirements.
Manages the design, documentation, testing, and implementation of clinical data collection tools
Develops data systems plans, guidelines, forms, manuals and SOPs
Assists in the preparation of clinical budgets
May supervise other Clinical Data Associates on assigned clinical trials and serve as Project Team Leader

Qualifications/Skills: Bachelors (BS) in technical or health care area with minimum of 7 years experience, or Masters (MS) in technical or health care area with a minimum of 5 years experience in clinical data processing within Data Management and thorough knowledge of clinical research. Data processing skills, technical expertise and elementary statistics knowledge required. Knowledge in database set-up required and experience with data review preferred. Experience with managing studies using EDC continuing education in clinical trial designs and monitoring procedures, FDA regulations and clinical data processing and reporting. Constructive interaction with inter and intradepartmental team members and personnel. Good organizational skills, problem-solving abilities, time management skills and initiative. Flexibility and ability to work on several assignments simultaneously. Must be able to work independantly as well as part of a team. Good written and oral communications skills in the English language. Must be precise, detail oriented, and able to detect subtle inconsistencies in the data. Must be able to develop new processes.

Location:	3000 Kent Avenue Suite A1-100 West Lafayette, IN 47906 United States