Associate Scientific Director Clinical Development - Endocrinology
Listed on 2026-09-18
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Management
At Recordati, we are united by a clear purpose: unlocking the full potential of life. With a century of history behind us, we are building the next chapter of our journey, continuing to grow while keeping patients at the centre of all we do.
What drives us is a shared belief that health, and the opportunity to live life to the full, should be within reach for everyone. This brings energy to our work, shaping how we support each other and show up every day. Our values – Better Together, Never Settle and Always Deliver – reflect this mindset, helping us to keep improving and make a meaningful difference.
Above all, these values bring to life our promise to everyone at Recordati, you can unlock your full potential. We know that people thrive when they can be themselves, are trusted and supported, and are given the opportunity to grow and make a meaningful contribution.
Are you ready to unlock your full potential?
This position is with Recordati Rare Diseases, Inc. (RRD), North America, an affiliate of Recordati.
Recordati Rare Diseases, Inc. (RRD) develops high-impact therapies for rare diseases, focusing on providing treatments to underserved communities in the U.S. Our mission is to mitigate the impact of rare diseases through increased awareness, better diagnoses, and improved treatment access in endocrinology, metabolic, hematology and oncology franchises. RRD is dedicated to fostering a dynamic work environment that promotes professional growth and a significant impact on patients' lives.
ReportingStructure
Reports To:
Medical Director, Endocrinology, NA
Direct Reports:
None
Areas Managed:
North America (U.S. and Canada)
The Associate Scientific Director, Endocrinology, NA (North America) is a key role in the delivery and support of many of the scientific activities required to support RRD’s Medical Strategy for the endocrinology franchise such as integrating Recordati’s scientific and clinical data into programs supporting medical affairs. They help interpret and communicate scientific topics, ensuring that scientific integrity and medical insights guide all their activities.
They are involved in delivering almost all aspects of externally facing medical communications and serve as subject matter expert for other roles in medical affairs (MA).
The Associate Scientific Director is directly responsible for delivering the following:
- Contributing to the Clinical Development plan, including identifying critical data gaps, defining evidence needs to support scientific objectives and key messages, and proposing data generation strategies that feed into the Scientific Data Evolution Plan.
- Supporting clinical trial protocol development as an endocrinology subject matter expert (SME), providing scientific and clinical guidance to ensure robust study design, methodological rigor, and alignment with clinical development objectives.
- Work collaboratively with evidence generation including clinical development and clinical operations on the design, execution, and interpretation of clinical trials in the endocrinology therapeutic area.
- Supporting clinical development regulatory interactions with the FDA, serving as the endocrinology SME providing scientific justification for study design, endpoints, and clinical rationale, and contributing to successful regulatory outcomes.
- Managing RRD’s Investigator Sponsored Studies (ISS) process, including tracking received applications, managing the review process, tracking the contracting process and conducting ongoing scientific communications with funded Principal Investigators (PIs).
- Working with PIs that have completed their ISS to provide, at the PIs request, scientific feedback on their outcomes communications and ensure dissemination of clinically relevant…
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