Job description
- As a Sr Clinical Data Coordinator at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified Clinical Data Managers to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP
- We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results
The role:
- Expertise in data management process
- You will be acting as a single point of contact (internal expert) for specific processing task(s) on a project
- You will be responsible for completeness, timely delivery and quality of clinical data
- You will lead and coordinate other team members within the department on assigned studies
- You will mentor project team members and be a subject matter expert when needed
- You will be managing project timelines, quality issues and justify out-of-scope.
What you need: bachelors degree, or educational equivalent, in clinical, biological or mathematical sciences, or related field, or nursing qualification with 5 + years of experience in core Clinical Data Management.
Benefits of Working in ICON:
- We offer very competitive salary packages. And to keep them competitive, we'regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
- We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
- But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
Role: Clinical research Scientist
Industry Type: Analytics / KPO / Research
Department: Research & Development
Employment Type: Full Time, Permanent
Role Category: Pharmaceutical & Biotechnology
Education
UG: Any Graduate
PG: Any Postgraduate
About company
We are a full service global contract research organization providing a broad range of product development and data solution services to pharmaceutical and biotechnology companies around the world. Our global operations span more than 75 offices across North America, Europe, Asia, Latin America, South Africa, Australia, and the Middle East. PRAs 16,400+ employees have participated in more than 3,800 clinical trials and have supported pivotal trials that led to U.S. Food and Drug Administration or international regulatory approval of more than 85 products since 2000.
