Clinical Project Lead

Carbyne; München; Vor Ort; EUR 100.000 - 125.000; Vollzeit

Zusammenfassung

A leading research institute in Munich is seeking a Senior Clinical Project Manager to lead innovative clinical research programs focused on minimal invasive diagnostics. This role involves guiding a cross-functional team, ensuring compliance with regulatory standards, and fostering relationships with key stakeholders. Ideal candidates should have a strong background in clinical project management, proven strategic thinking capabilities, and fluency in both German and English. This position offers an exciting opportunity to make significant contributions in a dynamic research environment.

Qualifikationen

• Proven track record in clinical project management in the pharmaceutical industry or academia in Germany.
• Knowledge of ICH GCP and regulatory guidelines in Germany.
• Fluent in German and English.

Aufgaben

• Lead the development of interventional clinical research program.
• Provide leadership to a cross-functional team.
• Identify and develop relationships with key stakeholders.

Kenntnisse

Administrative Skills

Facilities Management

Biotechnology

Creative Production

Design And Estimation

Architecture

Ausbildung

University degree in Life Sciences

Medical Doctor or PhD

Jobbeschreibung

A truly unique opportunity for a senior clinical project manager who would like to participate in something more exciting and creative than the daily routine of phase I - IV clinical study management.

Our client is a research institute -based on Nobel Prize winning technology- who are looking to revolutionize minimal invasive diagnostics in the upcoming years.

The purpose of the newly created Clinical Project Lead role is to build up and supervise their longitudinal clinical research program in Bavaria Germany.

Responsibilities

• Lead the development and execution of interventional clinical research program for non-IP diagnostic product.
• Provide program leadership to a cross-functional team.
• Identify and develop effective working relationship with key stakeholders sites and vendors.
• Provide innovative and flexible operational solutions to study design regulatory aspects resource management patient recruitment study & site management activities.
• Oversight of QA and Regulatory activities to ensure compliance with legislation and company standards.
• Liaising with Competent Authorities as necessary.

Requirements

• University degree in Life Sciences discipline (Medical Doctor or PhD is a plus)
• Proven track record in clinical project management in the pharmaceutical industry or academia in Germany
• Knowledge of ICH GCP and regulatory guidelines in Germany
• Proven ability to identify key stakeholder and build an effective clinical research network
• Demonstrated ability to think out-of-the-box and apply creative solutions to problems
• Ability to identify opportunities to accelerate results and build capability by assigning tasks to individuals with clear boundaries expectations and support
• Fluent German and English
• Strategic thinking and ability to translate high level objectives to an operational plan and setting smart objectives
• Role is based in Munich Germany

Please apply by uploading your CV or contact David Dobszay for further details.

Required Experience :

Senior IC

Key Skills

• Administrative Skills
• Facilities Management
• Biotechnology
• Creative Production
• Design And Estimation
• Architecture

Employment Type

Contract

Experience

years

Vacancy

1