Kelly Clinical Research has an immediate need for a Clinical Data Manager in Hazelwood, MO area. The Clinical Data Manager (CDM) is a member of the clinical research team responsible for data management activities across multiple trials. Activities include assisting in data entry, query processing, site management, data reporting and other data management activities in support of clinical trial projects. The CDM performs data management activities on both paper based and electronic data capture EDC studies. This is a 6-12 month contract position for someone who can start ASAP.
Job duties include:
CRF data review, preparation for entry, query processing, discrepancy management, ad hoc reporting and listing generation.
Develop study specific database requirements and edit check requirements with the help of Clinical Research Associates CRA and field monitors.
Create and maintain data management trackers and checklists for multiple projects.
Set-up and keep track of new sites, users across studies for EDC studies.
Assist in CRF design/development.
Assist with database design and validation activities for paper based trials.
Support with EDC study validation, user acceptance testing and implementation.
Assist in development of data verification audit listings and other audit activities.
Design case report forms.
Build database using Oracle Clinical and Remote Data Capture.
Assist in overall project tasks such as generating CRF completion guidelines, process flowcharts, Standard Operating Procedures SOPs, work instructions and training guidelines.
Support the team in any study startup and closeout activities including final report data QC.
Participate in project meetings to give a status update to project managers and upper management.
Assist in preparation of study material for investigator, study coordinator and monitor meetings.
Bachelor's degree in sciences or health profession or combined education and CDM experience equivalent.
5-8 years CDM experience.
Computer literacy in MS Word, Excel, PowerPoint, Access, Oracle Clinical, RDC and CRF design tools.
Ability to speak, write and understand English to comply with written procedures, instructions, SOPs and other documents.
Excellent organizational skills and attention to detail.
Ability to prioritize and multitask is a plus.
Ability to speak, write and understand English to comply with written procedures, instructions, SOP's.
Must be immediately eligible to work for any employer in the U.S. without restriction.
If you are a Clinical Data Management professional looking to make a move, please Apply Now and be sure to include a MS Word resume.
Note: All work must be done on-site, no work-at-home or telecommute option. No relocation assistance will be provided.
Kelly Clinical Research specializes in delivering clinical research workforce solutions to the world's leading pharmaceutical, medical device, and biotechnology companies, as well as contract research and site management organizations. We provide contract, temp-to-hire and direct hire opportunities. Areas we specialize in include Clinical Research Associates (In-house and Field-based), Data Management, U.S. and International Regulatory Affairs, Biostatistics and Analysis, Medical Writing, Project Management, GCP Audit and Quality Assurance, Clinical Operations and Support.
Kelly Services, Inc. is an Equal Opportunity Employer
This job has originated from a member site of TheJobNetwork - kellyservices.com. Category: Computer - Software, Keywords: Data Center Manager, Location: HAZELWOOD, MO - 63042