Primary Responsibilities
Ensures software applications are built with quality while conforming to corporate and regulatory processes and practices by
Ensures software applications are built on schedule and on budget by
Ensures software applications are effectively supported by
Maintains quality service and departmental standards by
Secondary Responsibilities
Contributes to team effort by
Maintains technical and industry knowledge by
Qualifications:
Education:
Bachelor s Degree strongly preferred
Experience:
1+ years of software development experience
Experience working with clinical trials and/or within pharmaceutical environment preferred
Working knowledge of the drug development process including knowledge of FDA requirements for GxPs and 21 CFR Part 11
Proven problem solving abilities
Additional skill set:
Ability to work in group setting and independently; ability to adjust to changing priorities
Unwavering commitment to service and product excellence
Strong interpersonal and communication skills, both verbal and written
Strong documentation and organizational skills
Ability to project and maintain a professional and positive attitude
Working conditions:
Travel: 0-5%
Lifting: 0-10lbs
Other: Computer work for long periods of time
EEO Statement
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Bioclinica is the leader in scientifically-driven services and technology-enabled solutions in clinical research. Clinical trials are complex, and traditional approaches are either monolithic or fragmented. Successful trials require an ability to see key details and uncover hidden insights. Empl...