Senior Clinical Trial Manager

Barrington James Limited; Hamburg; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

Barrington James Limited is seeking a (Senior) Clinical Trial Manager to lead clinical development programs in Hamburg. You will oversee study design, execution, and regulatory alignment, ensuring high-quality data and compliant processes across product development and launches.

Based on-site in Hamburg, the role offers opportunities to collaborate with cross-functional teams, manage study timelines, and drive efficient trial operations within a dynamic, globally focused environment.

Qualifikationen

• A degree in life sciences.
• 3+ years of experience.
• Ability to combine a hands-on mentality with a structured way of thinking.
• Experience working with SAP or any ERP system.

Aufgaben

• You will ensure the continuous proof of efficacy and safety for our completed products across all stages.
• Give accurate responses to scientific and regulatory questions related to trial design and evidence requirements.
• Showcase our clinical development in interdisciplinary generic development with an emphasis on clinical trials of medicinal products.
• Plan and supervise clinical and pre-clinical studies in line with regulatory guidelines and maintain high grade management of the whole program.

Kenntnisse

Hands-on mindset

Structured thinking

Ausbildung

Degree in Life Sciences

Tools

SAP

Jobbeschreibung

(Senior) Clinical Trial Manager

Location – Hamburg / On-site / Full-time

Job Function – Product Development / Launch Management

About the role

Combining your scientific knowledge with critical thinking, you’ll help build a high-quality development team. You’ll work closely with teams to push projects ahead efficiently. Become part of an exciting team where your work makes real change.

Responsibilities

• You will ensure the continuous proof of efficacy and safety for our completed products across all stages.
• Give accurate responses to scientific and regulatory questions related to trial design and evidence requirements.
• Showcase our clinical development in interdisciplinary generic development with an emphasis on clinical trials of medicinal products.
• Plan and supervise clinical and pre‑clinical studies in line with regulatory guidelines and maintain high grade management of the whole program.

About you

• a degree in life sciences
• 3+ years of experience
• Ability to combine a hands‑on mentality and a structured way of thinking
• Experience working with SAP or any other ERP system