Clinical Study Manager

**The Clinical Study Manager** is responsible for the day‑to‑day operational management of one or more clinical studies, including Investigational Device Exemption (IDE), post‑approval, post‑market surveillance, feasibility, marketing, and investigator‑initiated studies, in support of the **Trauma & Extremities Division** . This role partners cross‑functionally to ensure studies are executed efficiently, compliantly, and with high data quality to support evidence generation across the product lifecycle. The position is **R** **e** **mote** , with preference given to candidates located Eastern Standard Time (EST).

**What you will do**

+ Manage the day‑to‑day operational execution of clinical studies (IDE, post‑approval, post‑market, feasibility, marketing, and investigator‑initiated).
+ Contribute to study design and planning, including protocols, amendments, CRFs, monitoring plans, and operational procedures.
+ Ensure clinical study activities comply with r...