At a Glance
- Tasks: Manage and coordinate clinical trials while ensuring regulatory compliance.
- Company: Temple University, a leader in medical research and education.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on innovation in healthcare.
- Why this job: Play a crucial role in advancing medical research and improving patient care.
- Qualifications: Bachelor's degree and five years of regulatory compliance experience required.
The predicted salary is between 46000 - 52000 £ per year.
Temple University is seeking a Senior Regulatory Program Coordinator to manage and coordinate Phase I-IV clinical trials.
The role includes interacting with study sponsors and clinical staff within the Pulmonary/Critical Care/Sleep Med Department.
Ideal candidates must possess a bachelor's degree and five years of regulatory compliance experience.
Responsibilities include submissions to IRB and FDA, with a focus on maintaining communication with all stakeholders in the process.
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We think you need these skills to ace Senior Clinical Trials Regulatory Lead
Regulatory Compliance
Clinical Trials Management
IRB Submissions
FDA Submissions
Stakeholder Communication
Project Coordination
Attention to Detail
