PRO Consultant

R&D Partners; Stuttgart; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading consultancy in clinical trials is seeking a skilled PRO Consultant in Stuttgart, Germany, to drive Patient-Reported Outcomes strategies. The ideal candidate has over 5 years in the pharmaceutical sector, a track record with regulatory bodies, and expertise in PRO methodologies. Responsibilities include recommending PRO endpoints and collaborating with key stakeholders. This role demands advanced knowledge of integrating PROs into clinical studies, all aimed at enhancing trial outcomes and aligning with global standards.

Qualifikationen

• Minimum of 5 years of experience in the healthcare or pharmaceutical industry, specializing in PROs.
• Proven track record of successful applications of PROs with stakeholders like FDA, EMA, and HTAs.
• Advanced knowledge of PRO methods, instruments, and their integration into clinical studies.

Aufgaben

• Recommend PRO endpoints, instruments, and assessment schedules.
• Review statistical analysis plans for PROs.
• Collaborate with HEOR Asset Leads on PRO strategies.
• Contribute to Health Technology Assessment interactions.

Kenntnisse

Patient-Reported Outcomes (PRO)

Statistical analysis plans

Health Technology Assessment (HTA)

Jobbeschreibung

Shape the future of clinical trials by driving Patient-Reported Outcomes strategies that meet global standards and deliver real-world impact.

R&D Partners is seeking a skilled PRO Consultant to provide expertise in Patient-Reported Outcomes (PRO) within the pharmaceutical industry. This role focuses on designing and refining PRO strategies for clinical trials, ensuring alignment with strategic objectives and regulatory requirements. Please note that to be considered for this role you must have the right to work in this location.

Responsibilities

• Recommend PRO endpoints, instruments, and assessment schedules tailored to trial populations and strategic goals.
• Review statistical analysis plans for PROs to ensure alignment with protocol-defined endpoints.
• Collaborate with HEOR Asset Leads to refine PRO strategies based on evidence generation needs.
• Contribute to Health Technology Assessment (HTA) interactions as required.

Key Skills and Requirements

• Minimum of 5 years of experience in the healthcare or pharmaceutical industry, specializing in PROs.
• Proven track record of successful application of PROs with external stakeholders such as FDA, EMA, and HTAs.
• Advanced knowledge of PRO methods, instruments, and their integration into clinical studies during drug development.

For more information, please contact Seb Rose.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or visit the 'Contact Us' page.