|Publication date:||December 18 2020|
|Function Group:||Clinical Research|
For a full-service clinical contract research organisation (CRO), I am looking for a Site Contract Specialist. The organisation provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Their mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. They leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in the United States, employing approximately 3,500 people across almost 40 countries.
The organisation’s clinical operations activities are growing rapidly, and therefore they are currently seeking a full-time, office-based Contract Specialist, study start-up to join the clinical operations team. This position plays a key role in the study start-up and clinical trial management processes. The Site Contract Specialist will play a key role in advancing the start-up of many projects. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. You will serve as a liaison between sponsor, investigative sites and your co-workers. You will negotiate contracts and budgets with investigative sites, collaborate and work within a project team matrix to deliver results on time and keep up to date with applicable local regulations concerning clinical trials.
The ideal candidate has:
At this CRO, you will benefit from:
If you are interested in this job, or in similar ones, please feel free to contact me directly.
Senior Associate | Clinical Research