Clinical Data Manager I Job at Confidential, Grayslake, IL

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  • Confidential
  • Grayslake, IL

Job Description

job summary:

  • The Data Manager is a member of the Data Management and Analysis team responsible for supporting the successful delivery of data and processes conducted by CROs. This individual will collaborate closely with the Data Management & Analysis team and internal colleagues to ensure data integrity and quality in human clinical trials up through clinical proof of concept.
location: Grayslake, Illinois
job type: Contract
salary: $35.00 - 42.12 per hour
work hours: 9 to 5
education: Bachelors

responsibilities:

  • Provide CRO oversight and feedback related to the data management operations, issues and trends in performance
  • Completes assignments as delegated by Data Management relating to operational objectives and study deliverables
  • Effectively utilizes available technology, EDC platforms, Reporting and Visualization tools
  • Reviews CRO deliverable to ensure adherence to data standards and protocol requirements implemented within the design
  • Reviews study execution documents including specifications, data management plan, data review plan, data transfer plan and other cross functional plans delineating data review needs
  • Provide CRO oversight of data management tasks in adherence with established standards including third party vendor data reconciliation, medical coding processing, protocol deviation collection, and query management to identify errors and inconsistencies in clinical data and ensure their resolution
  • Identify and triage issues as they occur
  • Ensures CRO data management adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, and to data management quality standards.
 
qualifications:

  • Bachelor's degree in business, management information systems, computer science, life sciences or equivalent.
  • Must have at least 4+ years of pharmaceutical, clinical research, data management, health care or other relevant experience
  • Strong understanding of clinical trial processes and clinical technology
  • Demonstrated history of successful execution in a fast-paced environment and in managing multiple priorities effectively
  • Strong understanding of GCDMP
  • Demonstrated effective communication skills
  • Demonstrated effective problem-solving skills
 
skills: Good Laboratory Practices (GLP), Good Clinical Practice (GCP), CRO Oversight, Good Manufacturing Practices (GMP), International Council for Harmonization (ICH)


Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.


Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).


This posting is open for thirty (30) days.

Job Tags

Hourly pay, Contract work, Temporary work, Work experience placement, Local area

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