Clinical Research Associate

Job not on LinkedIn

🔥 0 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

Emerald Clinical

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2000

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Emerald Clinical is a leading global clinical research organization (CRO) founded in the Asia‑Pacific region that provides end‑to‑end clinical trial services to biopharmaceutical, medical device, and diagnostic companies. With about 25 years of experience and a team of 800+ operating across 40+ locations worldwide, Emerald Clinical manages trials across all phases including registration and post‑marketing studies, and offers clinical operations, project management, and trial staffing support. The company emphasizes scientific expertise, operational excellence, and global reach to support drug and device development.

📋 Description

• Coordinate investigator and site identification, feasibility assessment, and selection • Complete monitoring activities according to the Monitoring Plan and prepare monitoring visit reports • Plan, organize, conduct, and report on site evaluation visits • Prepare and submit regulatory packages and coordinate Ethics Committee packages • Manage site budgets, contracts, invoicing, and payments • Plan, organize, and conduct site initiation visits • Develop and maintain monitoring tools and project-specific documents • Motivate and train investigators and site personnel on protocols, investigational products, and trial requirements • Collect, review, approve, and code essential site documents for Trial Master File filing • Reconcile in-house Trial Master File and Investigator Site File contents • Coordinate distribution, tracking, handling, and destruction of investigational products and trial supplies • Maintain trial information in the clinical trial management system and tracking/reporting tools • Support strategies to improve trial recruitment

🎯 Requirements

• Tertiary qualifications in a related science or health care discipline • More than 2 years’ experience in on-site monitoring and site management in clinical trials is mandatory • Experience in academic, CRO, or pharmaceutical clinical trial environments • Experience in renal and/or oncology clinical trials is a plus • Practical knowledge of ICH-GCP guidelines and global and local ethical and regulatory research requirements • Competence in ethical and participant safety considerations, site start-up management, site conduct management, risk management, quality management, supply management, scientific concepts and clinical research design, and issue escalation management • Competence in negotiation and conflict resolution, critical thinking, problem-solving, decision making, and strategic thinking • Solid interpersonal communication and presentation skills • Ability to work autonomously and within a multidisciplinary team with varied stakeholders • Flexibility and adaptability amid changing priorities and ambiguous environments • Ability and willingness to travel

🏖️ Benefits

• Competitive compensation: tailored salary and benefits package • Hybrid or remote working arrangements, depending on location and role • Learning opportunities and access to a global network of scientific leaders • Employee wellbeing programs and initiatives supporting work-life balance, health, and team connection • Global engagement surveys • Recognition programs • Team-building events • Exposure to diverse projects and clients through international reach