IT ANLYST-CLIN DATA MGMT

Position code: 4198 Position Title: IT ANLYST-CLIN DATA MGMT



Work Location: New Jersey - Nutley Corporate Headquarters



Major Responsibilities:

Basic Function:

The Clinical Programmer provides study specific programming support as a member of the Data Management Services Team assigned to a clinical study. Responsible and accountable for all or part of the clinical programming activities within a study, assuring that activities are performed according to a quality standard and schedule agreed with the Study Management Team (SMT). This is achieved by representing Clinical Programming in one of the following roles: As an Assistant Clinical Programmer working to complete one or more of the clinical programming activities for a clinical study or as a Study Clinical Programmer working with the Project Clinical Programmer and the Study Data Manager to meet objectives and goals set by the SMT for a technically non-complex clinical study (e.g. one that does not require extensive clinical programming experience or resource). Ensures that detailed and database standards are implemented throughout the study and ensures the successful implementation of all clinical programming activities within a single clinical study.

Principal functional responsibilities:

? Leads or assists in the preparation and maintenance of study databases in accordance with project and global standards.

? Programs study-specific data validation checks.

? Produces ad-hoc listings and queries.

? Develops and maintains programs in a validated environment.

? Implements CP polices and procedures.

? Contributes to the updating of data management study documentation.

? Maintains knowledge of current, related Pharma Development and PDOx SOPs, Reference Manuals and guidelines.

Qualifications:

Qualifications and Experience:

? College/University degree - Bachelor of Science, Bachelor of Arts, or higher equivalent education in scientific, medical or relevant technical discipline

? One or more years experience in PL/SQL and/or SAS programming preferred.

? One or more years pharmaceutical experience preferred

? Knowledge of relational databases and experience using data management systems ? ORACLE/Clinical required

Planning and organizational skills

Fluent in English

Interpersonal Skills

? Team player

? Good interpersonal and communication skills

? Ability to organize, problem solve and work independently

? Detail oriented with the ability to prioritize multiple tasks efficiently

? Willing to be accountable and responsible for all assigned tasks.

Core Competencies:

Able to prepare clinical databases and related objects for the processing of routine clinical trials to ensure processing can be completed within a defined time frame.