Senior Clinical Data Specialist
hace 1 día
We are a leading healthcare intelligence and clinical research organization, shaping the future of clinical development.
This is an opportunity to work with our team as a Senior Clinical Data Specialist. As a key member, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to innovative treatments and therapies.
Your Key Responsibilities:- Developing tools for CDISC, Sponsor, and ICON standards implementation and compliance.
- Collaborating with cross-functional teams to define data collection strategies and standards for clinical trials.
- Creating and maintaining training and reference materials related to CDASH, SDTM, Terminology, ADaM, define-XML, and regulatory submission requirements.
- Managing data management processes and tools development and maintenance.
- Staying up-to-date with industry trends and regulatory updates related to data standards and integrating them into ICON's practices.
- You should possess a Bachelor's degree in a relevant field (e.g., Life Sciences, Computer Science, or related discipline); advanced degrees are a plus.
- You should have extensive experience in clinical data management and standards within the pharmaceutical or biotech industry.
- You should have advanced proficiency in CDISC standards and relevant regulations (e.g., FDA, EMA).
- You should have excellent analytical and problem-solving skills with attention to detail.
- You should have excellent communication and collaboration abilities to work effectively in cross-functional teams.
We offer a competitive salary range of 80,000 - 120,000 per year and a range of additional benefits focused on well-being and work-life balance opportunities for you and your family.
Our success depends on the quality of our people, which is why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
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