Senior Clinical Research Associate

Job not on LinkedIn

🔥 0 minutes ago

🦌 Connecticut, Maine, +5 more states – Remote

🦌 Connecticut – Remote 🦞 Maine – Remote 🗻 New Hampshire – Remote 🍂 Massachusetts – Remote ⚓ Rhode Island – Remote 🍁 Vermont – Remote ☕ Washington – Remote

⏰ Full Time

🟠 Senior

🔬 Research Analyst

Apply Now

Find Similar Remote Jobs

Receive Emails For Remote 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

TFS HealthScience - Contract Research Organization

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2007

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

TFS HealthScience is a leading global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies to advance clinical development. They offer a wide range of solutions including phase I-III clinical development, real-world evidence (Phase IV) studies, and strategic resourcing solutions. TFS HealthScience specializes in multiple therapeutic areas such as dermatology, internal medicine, neuroscience, oncology and hematology, ophthalmology, pediatrics, rare diseases, and orphan drugs. They aim to bring treatments to patients faster by combining their full-service capabilities and global reach with the flexibility and personalized approach of a mid-size CRO.

📋 Description

• Perform on-site and remote monitoring visits to ensure subject safety and data quality • Review CRFs and source documentation for accuracy and completeness • Ensure informed consent procedures and protocol compliance are met • Manage and track Investigational Product accountability • Prepare monitoring visit reports and follow up on action items • Maintain and update eTMF, CTMS, and trial documentation systems • Support sites with issue resolution and ensure timely completion of deliverables • Participate in audits and inspections, including preparation and follow-up • Collaborate with project teams and contribute to monitoring plans, project tracking, and CRA resource planning

🎯 Requirements

• Bachelor’s degree in Life Sciences, Nursing, or equivalent • Minimum 3+ years of CRA experience, including on-site monitoring • Strong understanding of GCP, ICH, and regulatory requirements • Experience working in a fast-paced, matrix organization • Excellent communication and organizational skills • Fluent in English • Strong attention to detail and problem-solving mindset • Ability to work independently and collaboratively • Experience in dermatology is considered a strong advantage.

🏖️ Benefits

• Competitive compensation package • Comprehensive benefits • Opportunity for personal and professional growth • Supportive work environment