Job summary
Job post source
This job is directly from Premier Research
Job overview
The Clinical Research Associate I role at Premier Research involves monitoring clinical trials to ensure data integrity and patient safety, supporting biotech and pharma companies in developing new medical products.
Responsibilities and impact
The role requires performing on-site and remote monitoring of clinical trials, ensuring data accuracy, managing site communications, reviewing investigational product accountability, identifying risks, and scheduling monitoring activities to meet study timelines.
Compensation and benefits
The starting base salary is $65,000 USD annually, with actual pay depending on qualifications; benefits include health insurance, retirement plans, and paid time off.
Experience and skills
Candidates should have an undergraduate degree preferably in Nursing or Medical fields, 3-5 years of clinical research or site coordinator experience, preferably in oncology, and must meet monitoring visit requirements and have a valid driver's license and passport.
Career development
Premier Research emphasizes growth by providing skills and opportunities to excel, supporting career development within the clinical research field.
Work environment and culture
The company values employee input, flexibility, work-life balance, and a collaborative environment focused on medical innovation.
Company information
Premier Research is a global clinical research organization supporting biotech, medtech, and specialty pharma companies in developing new medicines, devices, and diagnostics.
Team overview
The candidate will join the Global Clinical Monitoring and Site Management team, working closely with investigative sites and internal stakeholders.
Job location and travel
The position prioritizes candidates located in Texas and Illinois, with travel requirements for on-site monitoring visits.
Unique job features
The role offers opportunities to work across various therapeutic areas and includes both on-site and remote monitoring, emphasizing data integrity and patient safety.
Company overview
Premier Research is a global contract research organization (CRO) specializing in providing clinical development services to the biotechnology, pharmaceutical, and medical device industries. They make money by offering comprehensive clinical trial management, regulatory consulting, and data analysis services that help clients bring new therapies to market efficiently. Founded in 2002, Premier Research has a strong history of focusing on complex and rare diseases, leveraging their therapeutic expertise and innovative approaches to support the development of life-changing treatments.
How to land this job
Position your resume to highlight your nursing or medical degree, emphasizing any clinical research experience, especially as a site level coordinator or in oncology studies, to align with Premier Research's requirements for a Clinical Research Associate I.
Focus on showcasing your ability to perform monitoring activities with attention to data integrity, patient safety, and compliance with ICH-GCP/ISO 141155 standards, as these are critical aspects of the role.
Apply through multiple platforms, including Premier Research’s corporate careers page and LinkedIn, to increase your chances of being noticed for this role in the Central USA region.
Connect on LinkedIn with current Clinical Research Associates or team members in Premier Research’s Global Clinical Monitoring and Site Management division; use ice breakers such as asking about their experience working in specific therapeutic areas like oncology or rare diseases, or inquire how they balance remote and onsite monitoring duties.
Optimize your resume for ATS by incorporating keywords from the job description such as 'clinical monitoring,' 'data integrity,' 'patient safety,' 'ICH-GCP,' 'site management,' and 'oncology clinical trials' to ensure your resume passes initial automated screenings.
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