DCT Study Delivery Lead — Accelerate Trials

IQVIA; Bogotá; Presencial; COP 90.000.000 - 150.000.000; Jornada completa

Descripción de la vacante

IQVIA Colombia seeks an Associate Decentralized Clinical Trial Study Lead (aDCTL) / DCTL to oversee decentralised and hybrid DCT studies, coordinating with technology, mobile nursing, site operations and regulatory teams to deliver trials on time and within budget. You will set objectives, manage study delivery, monitor progress, lead risk and issue management, and present project information to stakeholders.

You will also mentor staff and participate in bid defenses as needed.

Formación

• Bachelor's degree in life sciences or related field.
• Plus 4+ years of clinical research experience with around 3 years in project management.
• Experience with electronic data capture (eDC) systems (CRFs) and data management.
• Broad knowledge of DCT and related trial delivery areas.
• Knowledge of clinical trial regulations including ICH GCP and local laws.
• Technology savvy with a track record of adopting new platforms.

Responsabilidades

• Strategically develop and deliver DCT studies aligning with contracts and budgets.
• Oversee DCT project relationships with customers and primary contacts.
• Set objectives and lead the study team per contract strategy and delivery approach.
• Collaborate across core study teams to prepare management plans and milestone delivery.
• Monitor progress and proactively present project information to stakeholders.
• Lead risk management, contingency planning, and issue resolution.
• Drive project quality and implement corrective actions when needed.

Conocimientos

Project management

Client facing

English communication

Budget management

DCT knowledge

Cross-functional collab

Educación

Bachelor's degree Life sciences

Herramientas

EDC (CRFs)

Data Management

Descripción del empleo

IQVIA Colombia seeks an Associate Decentralized Clinical Trial Study Lead (aDCTL) / DCTL to oversee decentralised and hybrid DCT studies, coordinating with technology, mobile nursing, site operations and regulatory teams to deliver trials on time and within budget. You will set objectives, manage study delivery, monitor progress, lead risk and issue management, and present project information to stakeholders.

You will also mentor staff and participate in bid defenses as needed.