Job summary
Job post source
This job is directly from ICON Strategic Solutions.
Job overview
As a Manager, Clinical Quality Compliance, you will oversee quality and compliance in clinical research, ensuring adherence to regulatory standards and supporting teams in risk management and inspections.
Responsibilities and impact
You will be responsible for addressing quality issues, providing training, developing SOPs, and collaborating with teams to ensure compliance with GCP and regulatory requirements.
Compensation and benefits
ICON offers a competitive salary along with various benefits including health insurance, retirement planning, and a global employee assistance program.
Experience and skills
Candidates should have a Bachelor's degree and at least 5 years of experience in a quality role within the pharmaceutical or CRO industry, with strong communication skills and regulatory inspection experience preferred.
Career development
ICON promotes a diverse culture that rewards high performance and nurtures talent, providing opportunities for professional growth and development.
Work environment and culture
The company values diversity, inclusion, and belonging, fostering an innovative environment to better serve its workforce and communities.
Company information
ICON is the world’s largest and most comprehensive clinical research organization, leveraging healthcare intelligence to drive success in clinical trials.
Company overview
ICON Strategic Solutions is a global provider of outsourced development and commercialization services to the pharmaceutical, biotechnology, and medical device industries. They specialize in clinical research, regulatory affairs, and market access, helping clients bring new treatments to market efficiently. The company generates revenue through contract research services, offering expertise in clinical trial management, data analytics, and regulatory compliance. Founded in 1990, ICON has grown through strategic acquisitions and partnerships, establishing a strong presence in over 40 countries and consistently ranking among the top CROs worldwide.
How to land this job
Tailor your resume to emphasize your experience with quality compliance in clinical operations, specifically highlighting your ability to manage complex operational challenges and your familiarity with GCP and regulatory requirements.
Showcase your leadership skills and problem-solving abilities, particularly in the context of developing processes, SOPs, and CAPAs, as these are crucial for the Manager, Clinical Quality Compliance role.
Apply through multiple platforms, including ICON's corporate site and LinkedIn, to maximize your chances of being noticed for this position.
Connect with individuals in the Clinical Quality division at ICON Strategic Solutions on LinkedIn, using ice breakers like asking about their experience with regulatory inspections or inquiring about recent quality initiatives they have been involved in.
Optimize your resume for ATS systems by incorporating specific keywords from the job description such as 'GCP', 'regulatory compliance', 'quality assurance', and 'risk management' to ensure it passes initial screenings.
Utilize Jennie Johnson's Power Apply feature to streamline your application process, as it can help tailor your resume, identify the best application channels, and connect you with relevant professionals in your target company.
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