RTSM Specialist, 12 Month Contract

🔥 22 minutes ago

🌐 United States, Canada – Remote

🇺🇸 United States – Remote 🇨🇦 Canada – Remote

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $71.5k - $142.5k / year

⏳ Contract/Temporary

🟡 Mid-level

🟠 Senior

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 0%

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Manage successful implementation of assigned RTSM systems or amendments according to client requirements, agreed time and cost frameworks, and company standards • Provide project management oversight from award through RTSM decommissioning • Oversee deliverables, timelines, and completion of work to Worldwide SOP standards • Communicate RTSM project activities to internal and sponsor study teams • Serve as escalation point of contact for assigned study-related project issues • Coordinate timely delivery of project communications, including study status reports, meeting agendas and minutes, and project call scheduling • Travel to Investigator Meetings or other project-related meetings when required • Manage overall RTSM project budget and ensure accurate vendor work orders • Manage overall RTSM study design • Write, review, and approve User Requirements Specifications (URS)

🎯 Requirements

• Ability to communicate concisely and effectively in both written and spoken English • Proficient client-facing skills • Proficient in the use of common office software • Self-motivated individual who can positively contribute to a team environment • High attention to detail • Ability to prioritize and handle multiple projects simultaneously • Educated to degree level in a relevant discipline or able to demonstrate equivalent experience • Minimum 2 years prior RTSM experience • Minimum 1 year prior project management experience • Minimum of 5 years experience within CRO /pharma environment • Contract Research Organization (CRO) or Pharmaceutical experience required • Familiar with RTSM topics, including RTSM study design, randomization methodologies, and just-in-time drug supply • Understanding of clinical trials, blinding, patient safety, data integrity and associated regulations • Proven ability to manage delivery of RTSM solutions deployed in clinical trials

🏖️ Benefits

• Competitive benefits package depending on location • Inclusive and equitable workplace • Transparent compensation and pay equity