Clinical Operations Specialist
hace 3 semanas
Role Overview
We are seeking a highly skilled Clinical Operations Specialist to join our team at Pharmiweb. As a Study Delivery Specialist, you will play a critical role in supporting the clinical trial team at the global level, impacting the project's success.
Key Responsibilities
- Maintain up-to-date knowledge on ICH GCP, sponsor's written standards, and attend relevant training sessions.
- Support multiple studies simultaneously, prioritizing tasks to meet business needs and ensure delivery of results.
- Manage access and study trackers, analyze reports, and distribute dashboards and reports to the study team.
- Provide system-related support, including TMF management and maintenance, and timely follow-up with stakeholders to improve TMF compliance.
- Work closely with SDS/SM to manage activities post-SAC and till final archival.
Requirements
- Excellent technical/IT skills, with the ability to understand the impact of technology on studies and use sponsor's systems/software effectively.
- Knowledge of ICH GCP relevant operational procedures, systems, and quality guidelines regarding clinical studies.
- Able to work independently and as part of a team, with a professional attitude and good customer focus.
- Very good communication skills, with high English language proficiency.
- 1-2 years of prior experience in clinical operations as CTA, CPA, or similar.
- Knowledgeable of main systems (vTMF, mCTMS) and the willingness and ability to continuously learn and become highly competent in using sponsor's evolving systems and tech.
What ICON Can Offer You
Our success depends on the quality of our people. We've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits, including well-being and work-life balance opportunities for you and your family.
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