CLINICAL DATA SPEC III

Location
Durham, NC
Posted
Apr 22, 2017
Institution Type
Four-Year Institution

CLINICAL DATA SPEC III
DCRI - CDI

POSITION SUMMARY
The Duke Clinical Research Institute in Durham, NC has an exciting opportunity for a experienced Clinical Data Specialist. The Clinical Data Specialist III (CDS III) independently plans, conducts and reports the data management portion of large, complex or international projects and provides leadership on the value and best practices for data integration processes. The CDS III provides the expert leadership for defining data management project requirements, considerations and effective implementation options. The CDS III position is an experienced manager supporting Clinical Data Management (CDM) teams, coordinating projects, facilitating infrastructure initiatives and participating in business development activities. The CDS III may perform other CDS level and Program Manager responsibilities on a project.

WORK PERFORMED
The CDS III independently plans and manages all project related data management activities to include project contracts and sponsor communication. The projects include international with multiple collaborators, partners or sub-contractors, and projects involving new technology. Project Management Budget/Scope of Work Contributes to the data management portion of the scope of work and protocol.

Provides input and assistance to Program Manager for scope of work changes. Oversees projections for project data management work.

Maintains accountability to the Project Lead for data management deliverables and timelines. Manages internal and external customer expectations. Risk Assessment Proposes solutions to project risks; collaborates with the Project Leader and/or Program Manager to manage risk. Communication

Oversees communication with Project Leader, project team, sponsor and project stakeholders regarding project data management items. Timelines Oversees CDM project specific timelines.

Coordinates with cross-functional team to develop and manage project timelines. Data Coordination EDC Support Oversees processes in support of EDC account management on projects.

Oversees coordination and resolution of project integration issues. (e.g., IxRS, SADI, data load issues).Manages project related issues.

Oversees project lock procedures for systems within the CDMS (e.g., EDC database, integrations).Audits Supports internal and external audits; develops and oversees execution of corrective action plan.

Stays current with applicable regulations and guidance. Project Documentation Oversees creation and management of the Data Management Plan throughout the project; may include complex project plans.

Supervises maintenance of project documentation in a centralized location for the duration of the project; to include, but is not limited to, a project profile, specifications, testing, and project data management training. Meetings Directs internal and external project team meetings that may include cross-functional groups, sponsors and external stakeholders (e.g., data management team meetings, on-line review).

Closeout
Oversees collaboration on project lock requirements and activities during closeout. Supervises the management of the project lock checklist. Therapeutic Area Knowledge Maintains a working knowledge of healthcare and research data that is collected in a therapeutic area. Training Oversees training on the EDC System, applications, and other project related data management activities.

Clearly defines project specific expectations, roles and responsibilities for all data management team members.

Oversees creation of eCRF instructions, training materials and other applicable CDMS instructions or other project related communication.

Prepares and makes presentations at internal and external meetings, including investigator meetings.

Technical CDMS Requirements
Oversees collaboration with project stakeholders on requirements and workflow of the CDMS (e.g., database, integrations, systems).EDC Database Requirements

Oversees database design and data validation checks with project stakeholders. Supervises collaboration with project stakeholders on best practices for data cleaning requirement sand requirements for reports/views, listings, quality control checks, alerts, data reconciliations and integrations.

Develops, programs and unit tests prototype eCRF screens and data validation checks. Standards Manages collaboration with sponsor and statistician to implement appropriate controlled terminology, standards, or use of sponsor data structures.

Development
Manages development, updates, and maintenance of specifications for project reports/views, listing, quality checks, alerts, data reconciliation requirements and integrations.

Oversees the programming and testing schedule in collaboration with CDM Technical Services and project stakeholders. Supervises review and approval of testing plan and testing results, and release of components into the production environment.

Oversees performance and documentation of quality control testing, user acceptance testing (UAT) and production qualification on components of the CDMS; oversees UAT with project stakeholders.

Production
Supervises all production activities on a project, including data cleaning, CDMS defects and changes, and data export services.

Administrative
Works with Program Managers to adequately resource project needs. Leads departmental initiatives. Coaches, mentors, and helps provide support to new project team members on project tasks.

Participates in screening, interviewing and hiring of team members.

Requisition Number
401252478

Location
Durham

Duke Entity
MEDICAL CENTER

Job Code
2355 CLINICAL DATA SPEC III

Job Family Level
68

Exempt/Non-Exempt
Exempt

Full Time / Part Time
FULL TIME

Regular / Temporary
Regular

Shift
First/Day

Minimum Qualifications


Education

Work requires organizational, analytical and communications skills generally acquired through completion of a bachelor's degree program.

Experience

Work requires four years of directly related data management experience.

OR AN EQUIVALENT COMBINATION OF RELEVANT EDUCATION AND/OR EXPERIENCE

Duke University is an Affirmative Action/Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, genetic information, gender, gender expression, gender identity, national origin, race, religion,sexual orientation, or veteran status.

Essential Physical Job Functions:Certain jobs at Duke University and Duke University Health System may include essential job functions that require specific physical and/or mental abilities. Additional information and provision for requests for reasonable accommodation will be provided by each hiring department.

Auto req ID

89200BR

Duke University is an Affirmative Action/Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, genetic information, gender, gender expression, gender identity, national origin, race, religion, sexual orientation, or veteran status.

Essential Physical Job Functions: Certain jobs at Duke University and Duke University Health System may include essential job functions that require specific physical and/or mental abilities. Additional information and provision for requests for reasonable accommodation will be provided by each hiring department.

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