Employer Industry: Healthcare Services

Why Consider this Job Opportunity:
- Competitive salary up to determined based on factors such as geographic location, work experience, education/training, and skill level
- Opportunity for career advancement and growth within the organization
- Comprehensive health insurance offerings for you and your family
- Global Employee Assistance Programme for 24-hour access to specialized professionals
- Flexible country-specific optional benefits to enhance work-life balance

What to Expect (Job Responsibilities):
- Support Study Clinical Scientist in medical surveillance and monitoring activities
- Analyze clinical trial data and assess issues related to protocol conduct and subject safety
- Assist in generating study safety events trackers and medical monitoring reports
- Participate in cross-functional study execution team activities
- Interact with internal and external stakeholders to support clinical trial objectives

What is Required (Qualifications):
- Life sciences degree (BS, MS, or Ph.D.) with clinical or pre-clinical research experience
- Experience in clinical data analysis, GCP, and clinical trial execution
- Proficiency in working with clinical trial sites
- Ability to make independent, timely decisions and handle multiple projects
- Excellent oral and written communication skills and strong computer/analytical skills

How to Stand Out (Preferred Qualifications):
- Experience in all stages of drug development
- High level of organizational and project management skills
- Flexible to accommodate changes in team and project needs

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