
Senior Clinical Study Manager
Há 3 dias
**Clinical Research Operations Specialist Role Overview**
">This role involves ensuring the safe and effective operation of clinical research studies. The Specialist is responsible for safeguarding the wellbeing of research subjects, reviewing study protocols, and executing procedures in accordance with protocols and regulatory standards.
">Clinical operations at this organization involve recruiting and coordinating communication with clinical trial volunteers and patients. This includes following applicable regulations globally and by region.
">The Specialist will collaborate with cross-functional teams to develop study materials, monitor trial progress, and address any issues that arise during the study.
">**Key Responsibilities:**
- ">
- Safeguarding the wellbeing of research subjects">
- Reviewing study protocols">
- Executing procedures in accordance with protocols and regulatory standards">
- Recruiting and coordinating communication with clinical trial volunteers and patients">
- Collaborating with cross-functional teams">
**Required Skills and Qualifications:
">* Strong organizational and communication skills
">* Ability to work under supervision
">* Attention to detail
">* Ability to handle routine tasks with some deviation from standard practice
">**Benefits:**
">Our organization is passionate about developing our people through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
">We are dedicated to taking care of our people and fostering a culture where you can authentically be yourself – unites us globally.
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