Remote Data Manager Consultant (Contractor) – Clinical Trials

ClinChoice; España; A distancia; EUR 55.000 - 96.000; A tiempo parcial

Descripción de la vacante

ClinChoice is seeking a Data Manager for an in-house contractor role in Spain. The Data Manager will lead DM activities for clinical trials, set up databases, and ensure timely, high-quality DM deliverables.

Collaboration with cross-functional teams will be essential to meet milestones and regulatory standards. The role requires 3+ years in data management within the pharmaceutical industry and hands-on experience with eCRF systems (Medidata Rave, Oracle InForm, OpenClinica, Medrio).

Formación

• Bachelor’s degree in clinical/pharmacy/biological sciences or related field or nursing degree.
• At least 3 years data management experience in pharmaceutical industry.
• Working knowledge of clinical research processes and regulatory terminology.
• Experience with eCRF systems (Medidata Rave, InForm, OpenClinica, Medrio).
• Ability to thrive in fast-paced environments and lead data management efforts.

Responsabilidades

• Lead data management activities for clinical trials and ensure timely, high-quality deliverables.
• Review protocol documents, CRFs, and develop eCRF specifications.
• Create and review Data Management Plans, Data Validation Plans, and data entry guidelines.
• Develop edit checks, query logic, and testing plans; train clinical teams and sites.
• Coordinate data reconciliation, database lock/unlock, and archiving processes.
• Maintain client satisfaction through quality, communication, and data integrity.

Conocimientos

Data management

Project coordination

Attention to detail

Communication skills

Leadership

Educación

Bachelor's degree in clinical/pharmacy/biological sciences or nursing

Herramientas

Medidata Rave

Oracle InForm

OpenClinica

Medrio

Descripción del empleo

ClinChoice is seeking a Data Manager for an in-house contractor role in Spain. The Data Manager will lead DM activities for clinical trials, set up databases, and ensure timely, high-quality DM deliverables.

Collaboration with cross-functional teams will be essential to meet milestones and regulatory standards. The role requires 3+ years in data management within the pharmaceutical industry and hands-on experience with eCRF systems (Medidata Rave, Oracle InForm, OpenClinica, Medrio).