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Clinical Research Associate; Oncology Monitoring Experience Required
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Job Description
- Req#: JR000420
Employer Industry: Clinical Research
Why consider this job opportunity:
- Competitive salary with potential for bonuses
- Opportunity for career advancement and growth within the organization
- Flexible work environment with the possibility of remote work
- Supportive and collaborative team atmosphere
- Chance to make a significant impact on clinical trial success and patient outcomes
What to Expect (Job Responsibilities):
- Conduct site monitoring responsibilities for clinical trials and ensure compliance with protocols
- Provide guidance and oversight to the CRA team, ensuring adherence to project scope and timelines
- Perform qualification, initiation, interim, and close-out visits, documenting monitoring activities
- Maintain regular contact with study sites to assess compliance and respond to sponsor requests
- Collaborate with cross-functional teams to resolve clinical trial monitoring issues
What is Required (Qualifications):
- Minimum of 2 years of oncology monitoring experience
- Graduation in a scientific health field (EU candidates)
- Ability to autonomously manage monitoring activities
- Strong organizational skills with the ability to multitask in a fast-paced environment
- Excellent communication and interpersonal skills with a customer service orientation
How to Stand Out (Preferred Qualifications):
- Certified Monitor in compliance with the Italian CRO decree (for EU candidates)
- Strong analytical and negotiation skills
- Experience with clinical trial management systems and electronic data capture
- Knowledge of clinical research, ICH GCP, and local regulations
- Ability to manage stress and work effectively in less structured environments
#ClinicalResearch #OncologyMonitoring #CareerOpportunity #RemoteWork #TeamCollaboration
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