About this opportunity
Collabera lists this Clinical Data Manager opportunity in maple grove, Minnesota. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Base pay range
$38.00/hr - $43.00/hr
Hiring: Pharmaceutical/Medical Device | Resumes to (No C2C/Vendors)
Position Details
Client: Pharmaceutical / Medical Devices
Position Title: Clinical Data Manager
Duration: 6 months Contract (Extension Highly Likely)
Location: Maple Grove, MN 55311 Onsite (Minimum 4 days/week)
Schedule: Daytime hours, 40 hours per week
Pay Range: $38.00-$43.00 per hour
Responsibilities
Oversee data management activities for 3-5 clinical trials from study start-up through trial closure.
Design and manage CRFs in alignment with clinical trial requirements.
Lead clinical data review, cleaning, and quality oversight activities.
Develop, document, and execute risk-based quality management strategies.
Identify study-specific risks related to data quality, trial conduct, and patient safety; implement mitigation plans.
Conduct central monitoring activities per approved monitoring plans.
Review clinical trial data to detect anticipated and unanticipated data issues.
Facilitate cross-functional discussions to assess findings and drive corrective action plans.
Serve as the primary data review liaison with therapy and clinical teams.
Ensure alignment between clinical requirements and technical data collection specifications.
Maintain documentation, including data management plans, risk assessments, and monitoring outputs.
Must Have
Bachelor’s degree in Biology, Health Sciences, Mathematics, Computer Science, or a related field. (No PhD)
Minimum 3 years of experience in clinical data management, clinical operations, or a healthcare-related field.
Hands‑on experience with clinical data management and data analysis (non‑statistical).
Direct experience overseeing multiple clinical trials simultaneously.
Strong knowledge of clinical trial data collection best practices.
Experience with risk identification, impact assessment, and mitigation planning.
Ability to translate clinical trial requirements into technical data specifications.
Experience conducting data review, central monitoring, and data cleaning activities.
Strong analytical, critical thinking, and problem‑solving skills.
Preferred
Certified Clinical Data Manager (CCDM) or equivalent certification.
Experience working in a global clinical operations environment.
Therapy‑specific knowledge of anatomy, physiology, pathophysiology, or medical devices.
Intermediate project management experience, including managing dependencies and accountability across teams.
Experience in a consultative or subject‑matter expert role influencing team decisions.
Benefits
Medical insurance
Dental insurance
Vision insurance
401(k) retirement plan
Life insurance
Long‑term disability insurance
Short‑term disability insurance
Paid parking/public transportation
Paid time, paid sick and safe time
Hours of paid vacation time
Weeks of paid parental leave
Paid holidays annually – subject to eligibility
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Worksite address
maple grove, MN, 55311, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.