Associate Director - Clinical Quality Assurance

February 8

🏖️ New Jersey – Remote

Although this job is listed in New Jersey, this company may be open to hiring remote in other states.

🏈 Ohio – Remote

Although this job is listed in Ohio, this company may be open to hiring remote in other states.

+2 more states

🏖️ New Jersey – Remote 🏈 Ohio – Remote 🍂 Massachusetts – Remote 🏰 Missouri – Remote

💵 $158.9k - $208.5k / year

⏰ Full Time

🟠 Senior

🔧 QA Engineer (Quality Assurance)

🦅 H1B Visa Sponsor

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Cision

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Cision is a global leader in media intelligence, offering a comprehensive suite of communications and PR solutions. The company's platform, CisionOne, provides media monitoring, analytics, and relationship management services to help clients understand, influence, and amplify their stories. Cision assists its customers in identifying and connecting with journalists and influencers, distributing meaningful public relations and marketing communications, and measuring their impact. With a range of brands including Brandwatch and PR Newswire, Cision supports PR and corporate communications, brand reputation management, social media insights, and investor relations.

PR Software • Social Media Software • Global Insights • GR & PAC Software

1001 - 5000 employees

Founded 2000

🤝 B2B

📱 Media

📋 Description

• The Associate Director, GCP Quality Assurance oversees GCP activities at Eisai, our CROs and Investigator Sites • Leads GCP audits and inspection readiness • Ensure high quality execution of clinical trials from first in human through commercial marketing authorization of clinical trials • Manage cross functional relationships with internal and external stakeholders • Be the Lead Quality Assurance representative to clinical teams • This is a high visibility position with great impact potential.

🎯 Requirements

• Bachelor’s degree in associated functional discipline, advanced degree preferred • Preferably 8+ years’ experience in Clinical research/operations/data management or related area • Minimum of 3-6 years of Clinical Quality Assurance auditing • Technical and administrative capabilities to independently carry out routine, complex and for-cause audits • Experience of inspection management • Experience with supervising direct reports preferred • Fundamental knowledge of US, EU and international regulatory standards and guidelines for the conduct of clinical trials • Strong analytical skills and report writing skills • Ability to demonstrate tact as a representative of the CQA Department • Must have professional communications skills, strong independent time management skills and the ability to manage multiple projects concurrently • Ability to Travel (approximately 25%)

🏖️ Benefits

• Eisai Inc. Annual Incentive Plan • Eisai Inc. Long Term Incentive Plan • Employee benefit programs