Clinical Research CTMS Specialist

🔥 9 minutes ago

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

The START Center for Cancer Research

WebsiteLinkedInAll Job Openings

501 - 1000 employees

🏥 Healthcare

💊 Pharmaceuticals

🧬 Biotechnology

Healthcare • Pharmaceuticals • Biotechnology

The START Center for Cancer Research is a global clinical research organization focused on early-phase oncology trials and advancing cancer therapies. START operates large, world-class research facilities across the United States and Europe and runs programs (such as the START Hope Hub) to help patients and families find, understand, and enroll in clinical trials. START serves patients, referring physicians, hospitals and oncology practices, and pharmaceutical partners, emphasizing broad access to clinical trials and translational cancer research.

📋 Description

• Serve as a liaison between the subject matter experts and the application core team to gather and communicate requirements which help define and verify application configuration • Translate (As applicable) calendars created by outside teams into START-approved calendars, including language translation for Spanish sites if necessary • Coordinates the activation of all new and legacy clinical trial calendar building and general study set up activities with internal and supporting external entities within the timeline parameters of Site Initiation Visits • Using Oncore®/Excel ®/Word, develops study tools, including but not limited to eligibility checklists, calendars and schedules, C1D1 checklists, supporting assessment tools, PK and EKG flow sheets (as required) and other documents as identified in collaboration with the Research Nurse, Study Coordinator and/or Principal Investigator • Updates pertinent Oncore Reviews data in a timely manner to facilitate Amendment receipt/approval, Consent /Re-Consent requirements and clinical trial status updates • Build strong relationships with project leadership, subject matter experts, clinical application colleagues and financial budget team members • Work with SMEs and project leadership to complete workflow decisions, workflow documentation, and supporting policies • Ability to understand the organization’s strategic priorities and adapt project timelines and tasks accordingly • Ability to escalate risks or issues effectively within the organization, if needed • Ability to identify and manage scope changes during the course of a project

🎯 Requirements

• Bachelor's Degree with at least 2 years of experience in the clinical research industry, or equivalent education and experience • Demonstrate accountability in project ownership and solution-oriented work approach • Creative problem-solving skills; ability to navigate through complex Phase I Oncology Protocols and apply to START’s Mission of quality data collection • Proven organizational skills including attention to detail and multi-tasking skills • Excellent verbal and written communication skills • Strong working knowledge of Microsoft Excel, Word, and PowerPoint

🏖️ Benefits

• Comprehensive health coverage: Medical, dental, and vision insurance provided • Robust retirement planning: 401(k) plan available with employer matching • Financial security: Life and disability insurance for added protection • Flexible financial options: Health savings and flexible spending accounts offered • Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided