Assistant Clinical Data Coordinator

Purpose: 1. Candidate will be responsible for the professional management and coordination of clinical trial data, on both an individual trial and project level (Phases I to IV)

2. Includes carrying out day to day data management / coordinating plans

3. Flexible with EDC experience

4. Responsible for edit checks; ensuring ongoing consistency; tracking status etc.

5. Identify errors and inconsistencies in CRF/eDC data and ensure their resolution in order that databases can be declared clean and locked according to ICH GCP standards

6. Ensure project documentation is reviewed and if appropriate contribute to the preparation of trial documents

7. High understanding of medical terminology, clinical trial methodology and ICH/GCP

8. Professional, positive and enthusiastic attitudeClassification:ContractCompensation:
based on experience HourJoin Aerotek Scientific LLCSM, one of the fastest growing providers of scientific and clinical research services in the nation. Due to our growth, we're constantly on the lookout for qualified professionals to place in contract, contract-to-hire, and permanent placement positions across the scientific and clinical research communities. At Aerotek Scientific, we know it's more than just your day-to-day responsibilities that can make or break a job. It's the support you get. That's the reason Aerotek Scientific offers a variety of benefits including medical, dental, optical, 401k, and many more. Don't put your career in the hands of just anyone, put it in the hands of a specialist. Join the Aerotek Scientific team! Allegis Group and its subsidiaries is an equal opportunity employer.

Required Qualifications:
Skills Requirements:
CRF Edits, Database Discrepency Check, ICH/GCP, Database Tracking, Pharmaceutical ExperienceContact Information
Contact:Beckman,Ryan