Employer Industry: Pharmaceutical Research and Development

Why consider this job opportunity:
- Competitive compensation with participation in short-term incentive programs
- Comprehensive benefits package including paid time off, medical/dental/vision insurance, and 401(k)
- Opportunity for career advancement in a leading R&D organization
- Engage in impactful work that contributes to solving serious health issues
- Collaborative and supportive work environment with a focus on innovation

What to Expect (Job Responsibilities):
- Monitor activities conducted by clinical investigative sites to ensure successful protocol execution
- Conduct site qualification, initiation, interim monitoring, and study closeout visits for Phase 1-4 studies
- Oversee site personnel activities and motivate them to achieve study objectives
- Ensure quality and timely submission of data from study sites, including safety event reporting
- Train study site personnel on protocols and regulatory requirements in collaboration with project teams

What is Required (Qualifications):
- Minimum of 1 year of clinically-related experience, with at least 6 months in clinical research monitoring
- Experience in on-site monitoring of investigational drug or device trials
- Willingness to travel to conduct on-site monitoring
- In-depth knowledge of regulations governing clinical research and ICH/GCP Guidelines
- Bachelor's degree is required

How to Stand Out (Preferred Qualifications):
- Experience in oncology clinical research monitoring
- Strong planning and organizational skills in a dynamic environment
- Demonstrated business ethics and integrity

#PharmaceuticalResearch #ClinicalTrials #CareerOpportunity #InnovativeMedicine #EqualOpportunityEmployer

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