Hybrid Oncology Clinical Data Coordinator

Actalent; United States; Hybrid; USD 39,000 - 44,000; Full time

Benefits offered by this job

Medical insurance

Dental & Vision

401(k)

Life Insurance

Disability insurance

HSA

Transit benefits

Employee Assistance Program

Paid time off

Job summary

Actalent is seeking a Clinical Research Data Coordinator in New Haven, CT to support oncology trials with data management and clinical coordination. The role blends data entry, source verification, scheduling, and regulatory compliance in a hybrid work environment.

You will work with EPIC, Medidata Rave, and ONCORE, ensure GCP/HIPAA adherence, and help prepare for monitoring visits while managing multiple studies.

Qualifications

• Minimum 2 years of clinical research or data management experience.
• Bachelor's degree in a related field or equivalent.
• Experience with EPIC and EMR/EHR systems.
• Strong data management, documentation, and source verification skills.
• Knowledge of GCP, HIPAA and IRB requirements.

Responsibilities

• Provide clinical and data management support for oncology trials.
• Enter, review, and maintain data in EDC systems and sponsor databases.
• Independently abstract and maintain study participant records.
• Coordinate patient care from recruitment through follow‑up and scheduling.
• Support monitoring visits by ensuring regulatory files are inspection‑ready.
• Collaborate with staff to ensure trial operations and timelines.

Skills

Clinical research experience

Data management

2+ years experience

Excel & Word

EMR/EPIC

Patient coordination

Data abstraction

GCP knowledge

HIPAA/IRB knowledge

Teamwork

Multitasking

Education

Bachelor's degree in related field

Tools

Medidata Rave

ONCORE

Job description

Actalent is seeking a Clinical Research Data Coordinator in New Haven, CT to support oncology trials with data management and clinical coordination. The role blends data entry, source verification, scheduling, and regulatory compliance in a hybrid work environment.

You will work with EPIC, Medidata Rave, and ONCORE, ensure GCP/HIPAA adherence, and help prepare for monitoring visits while managing multiple studies.