Description
Specific training in clinical research (CTA, GCP or other related courses) will be valued.
START Center for Cancer Research (“START”) is the world’s largest network of Phase I centers, exclusively dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global communities by offering them access to cutting-edge clinical trials in the United States and Europe. Today, with over 1,300 studies conducted and research centers in the United States, Spain, Portugal, and Ireland, START’s mission is to accelerate the development of new cancer therapies that improve quality of life and survival for cancer patients—and ultimately lead to their cure. To date, more than 43 therapies developed at START centers have received FDA/EMA approval.
Position available: **Data Coordinator**
**Responsibilities:**
* Assist with initiation visits for the clinical trials in which you participate
* Register patients in the sponsor’s IWRS/IVRS systems during screening and end-of-study
* Transfer data
* Resolve source document discrepancies
* Organize scheduled visits for each monitor
* Host monitoring visits
**Requirements:**
* Specific training in clinical research (CTA, GCP or other related courses) will be valued
* Proactive individual with strong organizational skills
* Excellent sense of responsibility and attention to detail
* Ability to work collaboratively and maintain effective communication with colleagues and supervisors
* Intermediate level of English
**Are you ready to join a team that will change the future of cancer treatment?**
Join us in our mission to defeat cancer—one clinical trial at a time. Your experience and dedication can help bring hope and healing to patients worldwide. Submit your application online.