Employer Industry: Pharmaceutical Research and Development

Why consider this job opportunity:
- Salary range will depend on various factors, including geographic location
- Comprehensive benefits package including paid time off, medical/dental/vision insurance, and 401(k)
- Eligible to participate in short-term incentive programs
- Opportunity to work in a dynamic environment with a focus on innovative clinical research
- Chance to make a significant impact on the development of life-changing therapies

What to Expect (Job Responsibilities):
- Monitor activities at clinical investigative sites to ensure adherence to protocols and regulations
- Conduct site qualification, initiation, interim monitoring, and study closeout visits for clinical studies
- Influence and motivate site personnel to meet study objectives and ensure regulatory compliance
- Ensure the quality and timely submission of data from study sites, including safety 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
- Required 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 Good Clinical Practices (GCP)
- Bachelor's degree is required

How to Stand Out (Preferred Qualifications):
- Experience in oncology clinical trials is preferred
- Strong planning and organizational skills to manage competing projects effectively
- Excellent analytical, interpersonal, and communication skills
- Demonstrated business ethics and integrity in previous roles

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