Clinical Data Manager — Onsite MN Contract (6 Months)

Experis Technology Group; Maple Grove (MN); Sur place; USD 59 000 - 63 000; Plein temps

Avantages offerts par ce poste

Medical and Prescription Drug Plans

Dental Plan

Vision Plan

401(k), Plus Match

Weekly Pay

Résumé du poste

ManpowerGroup’s Experis division is seeking a Clinical Data Manager in Maple Grove, MN to join a regulated clinical research organization. The role is onsite, with a 6-month contract, and pay is $43–$46 per hour on W2.

You will design and maintain clinical study databases, validate deliverables, and ensure compliance with standards and regulatory requirements. The ideal candidate has 5+ years in medical device/pharma/biopharma and 2+ years in a CDMS with study database setup and edit check

Qualifications

• Minimum 5 years of experience in a Medical Device, Pharmaceutical, or Biopharmaceutical company.
• Minimum 2 years of experience using a clinical data management system, including study database setup and edit check programming.
• Analytical and critical thinking skills with data management experience in regulated environments.
• Experience reviewing CRF design and protocol materials for accurate data capture.
• Ability to lead or participate in database setup and edit check programming.

Responsabilités

• Design, code, configure, test, debug, and document clinical study databases in line with SDLC.
• Develop and maintain clinical databases, validate deliverables, ensure regulatory compliance.
• Review CRF design and study protocol materials to support accurate data capture.
• Review database specification and Edit Check specs, provide feedback to improve data quality.
• Lead or participate in clinical study database setup and edit check programming.

Connaissances

Clinical Data Management

Database Setup

Edit Checks

Quality Assurance

Outils

EDC Systems

Description du poste

ManpowerGroup’s Experis division is seeking a Clinical Data Manager in Maple Grove, MN to join a regulated clinical research organization. The role is onsite, with a 6-month contract, and pay is $43–$46 per hour on W2.

You will design and maintain clinical study databases, validate deliverables, and ensure compliance with standards and regulatory requirements. The ideal candidate has 5+ years in medical device/pharma/biopharma and 2+ years in a CDMS with study database setup and edit check