Clinical Data Coordinator

Actalent; Detroit (MI); Hybrid; USD 60,000 - 75,000; Full time

Job summary

Actalent is seeking a Clinical Data Management Associate to support hematology/oncology Phase I studies in Detroit. You will collect and enter clinical data from EMR systems, coordinate monitor visits, and collaborate with coordinators, nurses, and regulatory staff in a growth-focused team.

The role emphasizes data accuracy, query resolution, audit prep, and adaptability in a hybrid 3 days onsite / 2 days remote schedule. Bachelor's degree required and EPIC familiarity preferred.

Qualifications

• Experience in clinical data management for research studies.
• Ability to collect and enter data from EMR systems, preferably EPIC.
• Familiarity with data queries, data cleaning and audits.
• Comfort working in oncology/hematology or Phase I trials.

Responsibilities

• Collect and enter clinical research data from EMR systems (preferably EPIC).
• Manage data uploads and maintain study databases.
• Resolve data queries and ensure data accuracy.
• Assist with audit preparation and regulatory compliance.
• Coordinate monitor visits and study documentation.
• Collaborate with cross-functional research teams.
• Support additional data and administrative activities as needed.

Skills

Data management

Data entry

Query resolution

Audit support

Regulatory awareness

Team collaboration

Organization

Education

Bachelor's degree

Tools

EPIC

Job description

Location: Detroit, MI (Hybrid: 3 Days Onsite / 2 Days Remote)

About The Role

Join a growing Hematology/Oncology research team supporting Phase I studies. This position focuses on clinical data management, including data entry, query resolution, audit preparation, and monitor visit coordination. You'll work alongside clinical coordinators, regulatory staff, and research nurses in a collaborative environment with strong growth potential.

Responsibilities

• Collect and enter clinical research data from EMR systems (preferably EPIC)
• Manage data uploads and maintain study databases
• Resolve data queries and ensure data accuracy
• Assist with audit preparation and regulatory compliance
• Coordinate monitor visits and study documentation
• Collaborate with cross-functional research teams
• Support additional data and administrative activities as needed

Required Qualifications

• Bachelor's degree
• 1+ year of experience with clinical research data management
• Experience collecting and entering data from EMRs
• Experience resolving data queries and supporting audits
• Familiarity with EPIC or a similar EMR platform
• Strong attention to detail and organizational skills
• Ability to work effectively in a team environment
• Adaptability and ability to manage changing priorities
• Oncology or Hematology research experience
• Phase I clinical trial experience