Madrid-based End-to-End Clinical Trial Leader

Jobtome; Madrid; On-site; EUR 65,000 - 90,000; Full time

Job summary

Novo Nordisk in Madrid is seeking a Trial Manager to lead assigned clinical trials from planning to close. You will translate strategy into action, drive cross-functional collaboration, and ensure trials meet quality and regulatory standards.

You will plan timelines, budgets, resources, oversee start-up, feasibility, and site performance, mentor the trial team, and work with investigators, hospital directors, and regional health authorities to advance our clinical research.

Qualifications

• Bachelor's or Master's degree in life sciences or related field.
• Experience in clinical trial project management in pharma or CRO.
• Ability to translate local insights into decisions and opportunities.
• Ability to lead across functions within a matrixed environment.
• Strong proficiency in digital tools and data analysis.

Responsibilities

• Plan and manage assigned clinical trials end to end, including timelines, budgets, resources and recruitment plans.
• Oversee trial start-up, feasibility, setup, management and close-out of trial systems with eTMF checks.
• Monitor trial performance using metrics and address risks with CAPAs.
• Lead cross-functional stakeholder management and represent the organization in trial meetings.
• Define submission strategies for regulatory authorities and ethics committees.
• Maintain quality through site visits and inspections readiness.
• Coach and mentor the clinical trial team on study protocols and procedures.

Skills

Clinical trial management

Strategic thinking

Leadership

Stakeholder management

Data analysis

Education

Bachelor's or Master's in life sciences

Tools

Digital tools

Job description

Novo Nordisk in Madrid is seeking a Trial Manager to lead assigned clinical trials from planning to close. You will translate strategy into action, drive cross-functional collaboration, and ensure trials meet quality and regulatory standards.

You will plan timelines, budgets, resources, oversee start-up, feasibility, and site performance, mentor the trial team, and work with investigators, hospital directors, and regional health authorities to advance our clinical research.