Senior Compliance Specialist, FSP

Job not on LinkedIn

🔥 17 hours ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🟠 Senior

🚔 Compliance

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🧬 Biotechnology

💊 Pharmaceuticals

🔬 Science

Biotechnology • Pharmaceuticals • Science

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Execute quality and compliance strategies and initiatives across the organization • Manage tracking, reporting, and documentation of quality and compliance activities • Lead quality processes and support process improvement initiatives • Mentor colleagues and collaborate across functional teams • Represent the department as a primary point of contact on assigned projects • Apply comprehensive knowledge of ICH GCP and applicable regulations to support clinical development programs

🎯 Requirements

• Bachelor's degree or equivalent combination of relevant education, training, and experience • 4+ years of relevant experience or an equivalent combination of education, training, and experience • Comprehensive knowledge of ICH GCP and applicable clinical research regulations • Proven project management experience managing clinical trial delivery activities • Excellent oral and written communication skills • Strong organizational and time-management skills • Demonstrated problem-solving and analytical skills • Ability to work independently and collaborate within cross-functional teams • Experience mentoring colleagues and leading project or process improvement initiatives

🏖️ Benefits

• Health insurance • 401(k) matching • Paid time off • Flexible work arrangements • Professional development opportunities