Cancer Clinical Research Coordinator - Protocols & Trials

Trinity Health; Silver Spring (MD); On-site; USD 38,000 - 61,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Mental health support

Paid time off

403B retirement plan

Education assistance

Voluntary benefits

Free parking

Job summary

Trinity Health in Silver Spring, MD is seeking a Clinical Research Coordinator to lead multisite protocol activities within the Cancer Program. You will ensure compliance with GCP, sponsor guidelines, and hospital policies while coordinating research teams and communicating findings.

The ideal candidate holds a Bachelor’s degree (Master’s preferred) with 3+ years in clinical research leadership, strong data management and presentation skills, and a valid driver’s license.

Qualifications

• Bachelor’s Degree required; Master’s Degree in a health-related field preferred.
• Active Driver’s License required.
• Good Clinical Practice (GCP) Certification preferred.
• Basic Life Support (BLS) Certification.
• Clinical research certification preferred.

Responsibilities

• Coordinates pharmaceutical company, NCI, multisite and in-house protocol activities for the Cancer Program.
• Adheres to federal regulations, sponsor guidelines, and hospital policies; supports required research work.

Skills

Cancer knowledge

Clinical protocols

Research leadership

Healthcare experience

Oral & written communication

Public speaking

Data analysis

Regulatory knowledge

Team leadership

Education

Bachelor’s Degree

Master’s Degree preferred

GCP Certification preferred

BLS Certification

Clinical research certification preferred

Job description

Trinity Health in Silver Spring, MD is seeking a Clinical Research Coordinator to lead multisite protocol activities within the Cancer Program. You will ensure compliance with GCP, sponsor guidelines, and hospital policies while coordinating research teams and communicating findings.

The ideal candidate holds a Bachelor’s degree (Master’s preferred) with 3+ years in clinical research leadership, strong data management and presentation skills, and a valid driver’s license.