Clinical Study Manager I: Quality, Enrollment & Compliance

Dm Clinical Research Group; Houston (TX); On-site; USD 85,000 - 110,000; Full time

Job summary

Dm Clinical Research Group in Houston, TX is seeking a Study Manager I to oversee clinical research activities at assigned investigative sites. The role ensures protocol adherence, data integrity, and timely enrollment aligned with sponsor expectations.

Responsibilities include site training, regulatory compliance, and cross-functional coordination to achieve study milestones. Strong written/verbal English required; bilingual English/Spanish preferred.

Qualifications

• Minimum 5 years of experience in Clinical Research.
• Supervisory experience preferred.
• Regulatory familiarity (FDA/ICH-GCP) preferred.

Responsibilities

• Ensure quality research at assigned investigative sites in line with sponsor protocol, FDA regulations and ICH-GCP guidelines.
• Train site staff, ensure adherence to ALCOA-C standards and timely documentation.
• Manage study activities from FPFV to study close out with cross-functional team coordination.
• Strive to meet sponsor enrollment goals and site-level performance metrics.

Skills

Attention to detail

Proactive

Written communication

Verbal communication

English proficiency

Bilingual English/Spanish

Education

High School Diploma

Bachelor's degree preferred

Foreign Medical Graduates preferred

Job description

Dm Clinical Research Group in Houston, TX is seeking a Study Manager I to oversee clinical research activities at assigned investigative sites. The role ensures protocol adherence, data integrity, and timely enrollment aligned with sponsor expectations.

Responsibilities include site training, regulatory compliance, and cross-functional coordination to achieve study milestones. Strong written/verbal English required; bilingual English/Spanish preferred.