Clinical Data Coordinator 2

Minimum Requirement

Bachelor’s degree or international equivalent in life sciences 

3-5 years of relevant work experience 

Level-Specific Responsibilities:

Performs study status tracking, data entry and verification.

Performs data review and quality control procedures.

Develops and provides input into project-specific guidelines. 

Performs data review, identification of data issues, and quality control procedures.

Participates in User Acceptance Testing.

Participates in the query management and data cleaning process.

Archives all study-related documents.

Provides advise or solutions in area of expertise.

May participate in audits and inspections.

Participates in project team meetings.

Skills Required:

Working knowledge of clinical research and the drug development process

Working knowledge of databases, tracking, validation, programming, word-processing and spreadsheet software

Working knowledge of clinical databases and query management

Working knowledge of organization procedures and policies and ensures actions comply.

Good written and oral communication skills

Good attention to detail

Good organization and time management skills

Ability to take a proactive approach to work

Ability to solve simple to moderate problems

Ability to multitask and prioritize work

Good ability to work in cross-functional teams

Developing professional expertise, applies company policies and procedures to resolve issues.

Works on routine problems of moderate scope. Exercises judgment following standard practices and procedures in analyzing situations or data from which answers can be readily obtained. Builds stable working relationships internally.

Receives occasional guidance on day-to-day work and moderate guidance on new projects or assignments.