Clinical Trial Manager III

🔥 41 minutes ago

🌐 South Korea, Malaysia, +2 more countries – Remote

🇰🇷 South Korea – Remote 🇲🇾 Malaysia – Remote 🇹🇼 Taiwan – Remote 🇹🇭 Thailand – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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

Fortrea

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Fortrea is a global clinical research organization (CRO) specializing in providing comprehensive clinical development services to biopharma and MedTech companies. With over 30 years of experience, Fortrea offers a range of services including clinical pharmacology, phase I-IV study management, regulatory strategy, market access, and more. They focus on advancing healthcare innovation by integrating data and scientific expertise to deliver tailored solutions that enable faster decision-making and improve patient outcomes, especially in the realm of cell and gene therapy programs, as well as various therapeutic areas like oncology, cardiovascular, and infectious diseases.

📋 Description

• Own end-to-end oversight of start-up and clinical responsibilities from site identification through database lock • Manage project scope, timelines, milestones, budget, quality, compliance, and country-specific commitments • Identify and address project, financial, quality, and operational risks • Forecast revenue, manage contracted scope, and oversee scope modifications • Track Key Project Indicators and ensure accurate resource projections • Develop site activation and recruitment strategies • Lead site identification and selection • Oversee informed consent form development and translations • Oversee essential document creation and collection, including insurance • Oversee Clinical Trial Agreement development, negotiation, execution, and site budgets • Lead regulatory and ethics committee submissions, approvals, and tracking • Ensure clinical and ancillary supplies, import/export logistics, and supply destruction processes are in place • Manage subject recruitment and retention, patient safety, vendor performance, and monitoring visit strategy • Plan monitoring activities to ensure data integrity, patient safety, and endpoint protection • Ensure inspection readiness through oversight of TMF, monitoring reports, protocol deviations, and issue management • Oversee and approve site payments and payment reconciliation • Foster communication and collaboration with clients and global cross-functional teams • Lead client-facing calls and communicate project status and operational control • Support new business through pre-award preparation • Provide training and support to new and junior team members • Perform other assigned duties

🎯 Requirements

• University/college degree (life science preferred) or certification in a related allied health profession (nursing, medical, or laboratory technology) from an appropriately accredited institution • Fortrea may consider relevant and equivalent experience in lieu of educational requirements • Fluent in English, both written and verbal • Five or more years of relevant clinical research experience in pharmaceutical, CRO, or health care setting • Comprehensive knowledge of GCP, ICH, and regulatory guidelines • Proficiency in Microsoft Office • Familiarity with EDC, CTMS, eTMF, and vendor platforms such as Veeva Vault and Medidata • Effective leadership in remote and global environment • Strong communication, planning, and organizational abilities • Proven team motivational skills • Proficiency in balancing concurrent tasks within time-sensitive environments • Financial awareness and use of tracking systems/tools • Demonstrated independent problem-solving and risk management mindset • Demonstrated professional client interaction and presentation skills • Ability to work independently and collaboratively • Preferred: Master’s or other advanced degree • Preferred: PMP certification or equivalent • Up to 20% global travel

🏖️ Benefits

• Remote-based work • Possible office presence depending on location • Up to 20% global travel, primarily domestic and international • EEO & accommodations support