Clinical Data Manager I#26-11128
North Chicago, IL
All On-site
Job Description
Hybrid Onsite, 4 days onsite
Purpose:
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.
Responsibilities:
o Provide CRO oversight and feedback related to the data management operations, issues and trends in performance
o Completes assignments as delegated by Data Management relating to operational objectives and study deliverables
o Effectively utilizes available technology, EDC platforms, Reporting and Visualization tools
o Reviews CRO deliverable to ensure adherence to data standards and protocol requirements implemented within the design
o Reviews study execution documents including specifications, data management plan, data review plan, data transfer plan and other cross functional plans delineating data review needs
o 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
o 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
Key Stakeholders:
Statistical Programming
Data Management
What are the top 3-5 skills, experience or education required for this position:
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
EEO:
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.
North Chicago, IL
All On-site
Job Description
Hybrid Onsite, 4 days onsite
Purpose:
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.
Responsibilities:
o Provide CRO oversight and feedback related to the data management operations, issues and trends in performance
o Completes assignments as delegated by Data Management relating to operational objectives and study deliverables
o Effectively utilizes available technology, EDC platforms, Reporting and Visualization tools
o Reviews CRO deliverable to ensure adherence to data standards and protocol requirements implemented within the design
o Reviews study execution documents including specifications, data management plan, data review plan, data transfer plan and other cross functional plans delineating data review needs
o 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
o 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
Key Stakeholders:
Statistical Programming
Data Management
What are the top 3-5 skills, experience or education required for this position:
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
EEO:
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.
Job ID: 518017817
Originally Posted on: 4/20/2026
Want to find more Biotechnology opportunities?
Check out the 14,459 verified Biotechnology jobs on iHireBiotechnology
Similar Jobs
Sign Up for Job Alerts
