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 to speak to one of our specialists visit the 'Contact Us' page.
R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.r-dpartners.com/privacy-policy/
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 to speak to one of our specialists visit the 'Contact Us' page.
R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.r-dpartners.com/privacy-policy/