Clinical Data Manager

TalentBurst; Maple Grove (MN); On-site; USD 76,000 - 117,000; Full time

Job summary

TalentBurst in Maple Grove, MN, is seeking a Clinical Data Manager for an on-site, 6-month contract. The role emphasizes data management, regulatory compliance, and collaboration across cross-functional teams.

The candidate will design and maintain clinical databases, review CRF designs, and ensure data quality through build, test, and validation activities. Strong experience in regulated studies and database programming is required.

Qualifications

• Minimum 5 years’ experience in Medical Device/Pharma/biopharma settings.
• At least 2 years configuring clinical databases and edit check programming.
• Experience with Oracle Clinical/Inform or similar preferred.

Responsibilities

• Follow software development lifecycle to design, code, configure, test, and document clinical study databases.
• Collaborate with development staff to ensure quality and consistency.
• Problem solver able to handle multiple tasks and escalate live errors.
• Participate in design reviews and provide feedback on CRFs and study databases.
• Lead or participate in setup of databases and edit checks in a clinical data management system.
• Work independently with minimal supervision while maintaining data integrity.

Skills

Analytical thinking

Communication skills

Leadership in discussions

Influencing team decisions

Tools

Oracle Clinical

Oracle Clinical Inform

Oracle Life Sciences Cloud

Job description

Clinical Data Manager

100 percent onsite-Location: Maple Grove, MN –6820 Wedgewood Rd N, MN 55311

Hours: Daytime Hours=40 per week

Duration: This is a 6-month contract with potential to extend highly likely

Please utilize attached Job Description for full job duties/requirements

Selected Candidate would start ASAP after screening clearance

Top Skills Needed

• Analytical and critical thinking skills along with related prior data management experience.
• Great communication skills with a focus on collaboration.
• Confident in leading discussions and managing complex regulated studies.
• Experience in effectively influencing a team decision to the desired outcome.

Clinical Data Manager

Our location in Maple Grove, MN currently has an on-site opportunity for a Study Database Manager – Data Management professional. The Study Database Manager is responsible for clinical database development and maintenance; validation of deliverables; adherence to processes, systems, standards, and best practices with attention to quality and regulatory compliance. Through cross-functional collaboration, the Study Database Manager will review Case Report Form (CRF) design, study protocol review and provide input. They will review database specification functional requirements and Edit Check specifications and provide feedback. They will lead and/or participate in set-up of clinical study databases in a clinical data management system including programming of edit checks. Ensure that standards and conventions are followed and data structure is fit for purpose for downstream reporting

What You’ll Work On

• Follow company software development lifecycle to design, code, configure, test, debug, and document clinical study databases using a clinical data management system.
• Collaborate with other development staff to achieve quality and consistency.
• Problem solver and decision maker with the ability to handle multiple tasks simultaneously.
• Actively participates in the escalation of live errors and service problems to limit downtime and resolve problems.
• Team player that develops high level design for solutions.
• Debugs, troubleshoots, and isolates clinical data management systems as well as offers strategic solutions, analysis, and advice regarding identified issues for future development.
• Ability to work creatively and productively with minimal supervision.
• Participate in the review of clinical research protocols, reports, and statistical analysis plans.

Required Qualifications

• Minimum 5 years’ experience working for a Medical Device, Pharmaceutical or Biopharmaceutical Company.
• Minimum 2 years’ experience using a clinical data management system performing clinical study database setup including edit check programming.

Preferred Qualifications

• Prior experience in study specific database configuration utilizing Oracle Clinical, Oracle Clinical Inform, or Oracle Life Sciences Cloud or other data management systems.
• Experience in adherence to FDA 21 CFR Part 11 and Guidance for Good Clinical Practices (GCP) data-handling procedures and guidelines.

Why TalentBurst?

At TalentBurst, we deliver more than talent, we deliver outcomes. We partner with you to move quickly and connect you to opportunities aligned with your skills and long term growth.

Backed by precision, transparency, and results, we connect top talent with leading organizations through trusted partnerships.

We offer competitive compensation and comprehensive benefits, including medical, dental, vision, and retirement options.

TalentBurst is an equal opportunity employer committed to an inclusive and diverse workforce.