Career Opportunities

Clinical Data Coordinator

Location: Flemington, NJ

Travel: Minimal

Description:

• Support data management project related tasks to ensure the study is run, reviewed and being coded effectively and efficiently and that discrepancies are reported in a timely and appropriate manner.

Responsibilities

• Assume responsibility for the reviewing and coding of case report form:
• Participate in the development of case report forms, case report form completion guidelines, edit checks, data entry guidelines, coding guidelines, and data review guidelines to ensure compliance with Beardsworth data management standards and the study protocol.
• Ensure consistency in reviewing and coding within a project.
• Document exceptions to guidelines once approved by the project team.
• Authorize corrections to the database:
• Generate standard edit checks and data review listings.
• Collaborate with client/clinical operations to properly evaluate data.
• Update database based on response received.
• Assume primary responsibility for the execution of assigned projects:
• Maintain project file, in accordance with client standard operating procedures, to document all data management related study procedures.
• Generate data resolution queries.
• Convey progress of critical data management activities to project team.
• Create and/or run standard programs to ensure data integrity.
• Create Data Management Plans.
• Communicate/coordinate with project manager, statistician, clinical research associate, database manager to ensure clean database.
• Interact with clients as necessary.

Qualifications

• Proficient in MS Outlook, Word, Excel, PowerPoint. Knowledge of relational database structure. Familiarity with MS Internet Explorer. Some SQL/SAS, MS Access, MS Project is helpful
• Ability to work with minimal supervision.
• Strong attention to detail.
• Possess excellent written and verbal communication skills.
• Solid experience with EDC
• Bachelor’s degree in life sciences or RN preferred or equivalent work experience.
• Minimum of 3-5 years clinical data management experience from a pharmaceutical or biotech company or CRO. Lab or Nursing experience preferred.

Please contact or fax your CV, with salary requirements and contact information to Human Resources at (908) 806-5992.