Clinical Data Manager

Base pay range

$38.00/hr - $43.00/hr

Hiring:
Pharmaceutical/Medical Device | Resumes to  (No C2C/Vendors)

• 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

• 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.

• 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.

• 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.

• 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