Clinical Trials Study Manager: Lead Data & Compliance

DM Clinical Research; Tomball (TX); On-site; USD 80,000 - 100,000; Full time

Job summary

A clinical research organization is seeking a Clinical Research Study Manager to ensure high-quality research is conducted at investigative sites. The role involves overseeing training for site teams and maintaining compliance with FDA regulations. Candidates should have a minimum of 5 years in clinical research and preferably possess supervisory experience. Excellent detailed-oriented skills and effective communication abilities in both English and Spanish are essential. This position is located in Tomball, Texas and aims to meet enrollment goals and ensure data quality.

Qualifications

• Minimum of 5 years of experience in Clinical Research.
• Supervisory experience preferred.
• ACRP or equivalent certification is preferred.

Responsibilities

• Ensure quality research is conducted at assigned sites.
• Maintaining knowledge of current FDA regulations.
• Responsible for training site teams in protocol procedures.

Skills

Detail-oriented

Strong written communication

Customer service skills

ProACTIVE

Goals-driven

Education

High School Diploma or equivalent

Bachelor's degree

Tools

Clinical Trial Management Systems

Electronic Data Capture

Job description

A clinical research organization is seeking a Clinical Research Study Manager to ensure high-quality research is conducted at investigative sites. The role involves overseeing training for site teams and maintaining compliance with FDA regulations. Candidates should have a minimum of 5 years in clinical research and preferably possess supervisory experience. Excellent detailed-oriented skills and effective communication abilities in both English and Spanish are essential. This position is located in Tomball, Texas and aims to meet enrollment goals and ensure data quality.