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Clinical Safety Reporting Specialist
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Job Description
- Req#: R13533
Employer Industry: Medical Technology
Why consider this job opportunity:
- Salary up to $120,000
- Eligible for the Medtronic Incentive Plan (MIP)
- Comprehensive benefits package supporting various career and life stages
- Opportunity for career advancement and growth within a global healthcare leader
- Collaborative work environment focused on innovation and problem-solving
- Chance to make a significant impact on healthcare access and equity
What to Expect (Job Responsibilities):
- Ensure consistent assessment of Clinical Safety data against reporting requirements
- Interact with investigational sites and clinical monitors to gather necessary Clinical Safety information
- Collaborate with Regulatory Affairs and Clinical Operations for timely reporting of Clinical Safety data to authorities
- Act as a liaison for Clinical Safety-related inquiries from study teams and sites
- Support study audits related to Clinical Safety topics
What is Required (Qualifications):
- Bachelor's degree with 2+ years of clinical research experience or an advanced degree with no experience
- Strong understanding of Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials
- Familiarity with medical terminology
- Ability to work collaboratively with cross-functional teams
- Excellent communication skills
How to Stand Out (Preferred Qualifications):
- Previous experience with the employer
- Background in safety reporting or clinical safety
- Knowledge of regulatory requirements specific to clinical trials
- Experience in clinical research settings
- Proficiency in data analysis and report preparation
#MedicalTechnology #ClinicalResearch #HealthcareCareers #CompetitiveSalary #InnovationInHealthcare
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