Clinical Data Manager
| Posted On: Nov 21, 2025
Maple Grove, MN 55311
6 Months, Contract
On-site
Job Summary
- Job Title:
- Clinical Data Manager
- Posted Date:
- Nov 21, 2025
- Duration:
- 6 Months, Contract
- Shift(s):
-
09:00 - 18:00
- Salary ($):
- 42.35 - 44.52 per Hourly (compensation based on experience and qualifications)
- We care about you! Explore Rangam’s benefits information
Description
Main Purpose Of Role
- The Clinical Data Manager is responsible for managing the development, documentation, and execution of risk-based quality management systems, as described in the risk assessment, data management plan, and site and central monitoring plans.
- As the customer-face of Data Review and its primary liaison with the therapy group, the Clinical Data Manager's therapy-specific knowledge ensures alignment to customer definitions of criticality, and informs review and analysis of study data.
Main Responsibilities
- Identification of study specific risks to study conduct and human subject safety; analysis of risks; development and implementation of mitigation strategies.
- Review of study data to detect anticipated and unanticipated issues related to trial data completeness and quality.
- Facilitate multi-stakeholder discussions to review findings, evaluate impact and develop action plans for correction and continued monitoring.
- Conduct Central Monitoring activities, as described in Central Monitoring Plan.
- Direct all data cleaning activity related to assigned studies.
Qualifications
- Bachelors Degree (± 16 years)
- Biology, Health Sciences, Mathematics, Computer Science, or equivalent.
Experience/Background
- 3 years in clinical operations or healthcare related field.
- Education and work experience in project management, life sciences and/or technical field.
- Knowledge of data collection best practices for clinical trials.
- Knowledge of global clinical operations.
- Experience in consultative role, with Subject Matter Expertise, and effectively influencing a team decision to the desired outcome.
- Proficient at the identification of risks in a process, evaluation of likelihood and impact, and the development of effective mitigation and monitoring strategies that are imperfect yet meet the business need.
- Proficient in the translation of clinical trial requirements to the technical specifications required for effective data collection.
- Skilled at making inferences and connections based on limited information, clearly describing the knowns, unknowns, and alternative explanations.
- Intermediate project management skills; developing a multifaceted plan with complex dependencies and holding peers accountable to adherence to the plan while maintaining positive and collaborative relationships.
- Intermediate therapy specific knowledge of anatomy, physiology, pathophysiology, therapy and device.
Licenses and Certifications
- None required; Certified Clinical Data Manager (CCDM) or equivalent nice to have.