Senior Clinical Data Manager — Lead CDM Projects (Remote)

mmsholdingsinc; Ciudad de México; A distancia; MXN 1.086.000 - 1.628.000; Jornada completa

Descripción de la vacante

MMS Holdings, Inc. is seeking an experienced Senior Data Manager to lead data management efforts across studies. You will coordinate with clients and suppliers, oversee end-to-end data management activities, and ensure adherence to GCP/ICH and FDA guidelines.

Mentorship and cross-functional collaboration are key aspects of the role. You will manage data from study set-up to close-out, including CRF tracking, data validation, query resolution, and documentation, while ensuring timely delivery and

Formación

• Bachelor’s or Master’s Degree in scientific or health care field preferred with industry or relevant experience.
• 5+ years’ experience in data management with at least 1 year leading projects.
• Extensive knowledge of paper CRF study systems, EDC, and hybrid CDM systems.
• Excellent verbal and written communication skills and strong organizational abilities.

Responsabilidades

• Oversee data management study processing from start-up to close-out with client coordination.
• Act as primary DM contact; manage CRF tracking, data entry, and QA activities.
• Provide mentorship and training to junior data managers and DM staff.
• Lead protocol review discussions and ensure regulatory compliance (GCP/ICH, FDA).
• Develop DM study documentation and perform UAT with cross-functional teams.
• Ensure timely delivery of study tracking metrics and project timelines.

Conocimientos

EDC systems knowledge

Data management leadership

Client and vendor communication

Independent work

Cross-functional collaboration

Educación

Bachelor’s or Master’s Degree in scientific or health care field

Herramientas

CRF study systems

CDM data tools

Data management platforms

Descripción del empleo

MMS Holdings, Inc. is seeking an experienced Senior Data Manager to lead data management efforts across studies. You will coordinate with clients and suppliers, oversee end-to-end data management activities, and ensure adherence to GCP/ICH and FDA guidelines.

Mentorship and cross-functional collaboration are key aspects of the role. You will manage data from study set-up to close-out, including CRF tracking, data validation, query resolution, and documentation, while ensuring timely delivery and