Clinical Research Coordinator I - Precise Trial Coordination

Cenexelresearch; Marlton, Northern (NJ, KY); Hybrid; USD 36,000 - 45,000; Full time

Benefits offered by this job

Health Insurance

Dental

Vision

LTD

STD

Life Insurance

401k

Job summary

CenExel Clinical Research in Marlton, NJ is seeking a detail-oriented professional to assist with coordinating clinical trials in accordance with ICH and GCP guidelines. The role supports study initiation through completion and ensures regulatory compliance.

Responsibilities include organizing research information, data collection, adverse event documentation, safety assessments, and communication with sponsors. A Bachelor's degree is preferred and 0–3 years in clinical settings.

Qualifications

• Bachelor's degree preferred; high school graduation or equivalent acceptable.
• 0–3 years in the medical field.
• Knowledge of Federal regulations protecting human subjects in research and good clinical practice.

Responsibilities

• Assist coordination of patient involvement from study initiation to completion.
• Organize research information for clinical trials.
• Observe subjects and assist with data analysis and reporting.
• Schedule data collection activities.
• Document adverse events, protocol deviations and other issues.
• Report research data to maintain quality and compliance.
• Perform administrative and regulatory duties related to the study.
• Participate in protocol development activities.
• Ensure site receives accurate information and supplies from sponsors.

Skills

Leadership

Mentorship

Communication

Teamwork

Crisis management

Education

Bachelor's degree

Job description

CenExel Clinical Research in Marlton, NJ is seeking a detail-oriented professional to assist with coordinating clinical trials in accordance with ICH and GCP guidelines. The role supports study initiation through completion and ensures regulatory compliance.

Responsibilities include organizing research information, data collection, adverse event documentation, safety assessments, and communication with sponsors. A Bachelor's degree is preferred and 0–3 years in clinical settings.