Director, Clinical Data Management: Drive Data Integrity

The Steely Group

Boston (MA)

Sur place

USD 100 000 - 140 000

Plein temps

14 jours+
Générateur de candidature

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Résumé du poste

A leading clinical research organization is seeking a Director of Clinical Data Management to oversee all data management activities for clinical trials. This role ensures data integrity, compliance, and quality throughout the data lifecycle. Responsibilities include leading cross-functional teams, overseeing CRO performance, and managing the creation of key clinical documents. The ideal candidate has a degree in health sciences or a related field, approximately five years of experience, and strong expertise in clinical trial processes and data management principles.

Qualifications

  • Bachelor’s degree in a relevant scientific discipline.
  • Approximately 5 years of clinical data management experience.
  • Strong expertise in data management principles and regulatory requirements.

Responsabilités

  • Lead data management activities across clinical trials from start-up to database lock.
  • Ensure compliance with regulatory standards and data integrity.
  • Oversee performance and quality metrics of CROs.

Connaissances

Clinical trial processes
Data management principles
Regulatory requirements
SQL
GCP
Communication skills
Analytical skills

Formation

Bachelor’s degree in health sciences, life sciences, mathematics, computer science, or related discipline

Outils

Electronic Data Capture (EDC) systems
SAS
R
Python

Description du poste

A leading clinical research organization is seeking a Director of Clinical Data Management to oversee all data management activities for clinical trials. This role ensures data integrity, compliance, and quality throughout the data lifecycle. Responsibilities include leading cross-functional teams, overseeing CRO performance, and managing the creation of key clinical documents. The ideal candidate has a degree in health sciences or a related field, approximately five years of experience, and strong expertise in clinical trial processes and data management principles.
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