Hybrid Oncology Data Coordinator - Impactful Trials

Actalent; United States; Hybrid; USD 39,000 - 43,000; Full time

Benefits offered by this job

Medical coverage

Dental coverage

Vision coverage

401(k) retirement plan

Life Insurance

Disability benefits

Health Savings Account (HSA)

Transportation benefits

Time Off/Leave

Job summary

Actalent is seeking a Clinical Research Data Coordinator to support oncology trials in New Haven, CT. You will manage data collection, entry, and reporting in EDC systems and sponsor databases, ensuring accuracy and regulatory compliance.

The role requires collaboration with cross-functional teams, prioritization in a fast-paced environment, and strong documentation practices across recruitment, treatment, and follow-up phases.

Qualifications

• Two years of related work experience in clinical research, data management, or a similar role.
• Bachelor's degree in a related field or equivalent education and experience.

Responsibilities

• Provide clinical and data management support for oncology clinical trials.
• Enter, review, and maintain data in EDC systems and sponsor databases.
• Abstract, create, and maintain study participant records with source verification.

Skills

Clinical research coordination

Data management

GCP knowledge

HIPAA familiarity

IRB understanding

EDC systems

Multitasking

Attention to detail

Team collaboration

Education

Bachelor's degree in a related field

Tools

EPIC

Medidata Rave

ONCORE

Oracle-based systems

Job description

Actalent is seeking a Clinical Research Data Coordinator to support oncology trials in New Haven, CT. You will manage data collection, entry, and reporting in EDC systems and sponsor databases, ensuring accuracy and regulatory compliance.

The role requires collaboration with cross-functional teams, prioritization in a fast-paced environment, and strong documentation practices across recruitment, treatment, and follow-up phases.