Clinical Data Entry Jobs in New Jersey

Proven experience with research as well as knowledge of best practices for HIPAA, consent, GCP, FDA, SOP, safety monitoring, and others.

Competitive wage plus great benefits - medical/dental/vision, 401(k) match, etc.

Ensure compliance, create reports, and prepare for sponsor and regulatory manager visits.

Bachelor’s degree in related science field or equivalent amount of clinical research experience in the given study area.

CCRA, CCDM, CCRC, or CCRP certification required.

Strong communication skills and ability to collaborate with a team.

Primary Duties and Responsibilities include the following:

4. Develop, institute and manage initiatives and strategic plans in response to trending data

7. Manage employee and departmental timeliness and progress during development and implementation of new initiatives

8. Measure and manage staff compliance with new processes and overall success of programs

12. Maintain clinical department files for staff credentialing, licensure and education

14. Manage departmental schedules and communications

Minimum of 4+ years of relevant clinical data management experience in the pharmaceutical/biotech industries and college degree

Strong communication skills required, and experience working remotely is highly preferred

Experience performing clinical data review and data reconciliation, as well as handling review and reconciliation of data discrepancies

Good working knowledge of ICH, FDA, and GCP regulations and guidelines

Expertise working within the Medidata RAVE EDC system

Must be based on the East Coast and/or able to accommodate full East Coast working hours