Senior Clinical Data Systems Lead for Study Build & EDC

Collabera; North Chicago (IL); On-site; USD 94,000 - 104,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) retirement plan

Life insurance

Short/Long-term disability insurance

Paid parking/public transit

Paid time off

Job summary

Collabera is seeking a senior professional to provide technical leadership for the design, development, and delivery of clinical trial systems and data standards. You will support study and program level activities across clinical development programs and ensure systems meet protocol requirements, data standards, and regulatory expectations.

The role involves coordinating technical study build activities, system integrations, timelines, dependencies, and quality requirements, while contributing

Qualifications

• Bachelor’s degree or equivalent in Life Sciences, MIS, CS, or related field.
• Seven+ years of hands-on technical study build experience in electronic data capture systems.
• Experience with Medidata Rave is required.
• In-depth knowledge of clinical trial processes and data standards.
• Ability to influence stakeholders in a matrixed environment.

Responsibilities

• Lead technical study build activities within EDC clinical trial systems.
• Design and develop clinical trial systems based on protocol requirements and data standards.
• Coordinate delivery of new clinical systems and integrations.
• Monitor study progress, timelines, risks, and deliverables using PM tools.
• Mentor team members and contribute to process improvement initiatives.

Skills

CDISC SDTM

Regulatory compliance

Stakeholder influence

Analytical skills

Strong communication

Education

Bachelor’s degree in Life Sciences/Computer Science

Tools

Medidata Rave

Job description

Collabera is seeking a senior professional to provide technical leadership for the design, development, and delivery of clinical trial systems and data standards. You will support study and program level activities across clinical development programs and ensure systems meet protocol requirements, data standards, and regulatory expectations.

The role involves coordinating technical study build activities, system integrations, timelines, dependencies, and quality requirements, while contributing