đ Launch Your Career in Clinical Trial Operations
Join Emerald Clinical Trials as a Clinical Trial Specialist and become an essential part of our Clinical Operations team. In this dynamic role, you'll develop expertise in clinical trial start-up processes, TMF management, and regulatory compliance while contributing to meaningful research in renal, cardiometabolic, and oncology therapies. This is your opportunity to build a foundation for a rewarding career in clinical research.
đŻ Your Impact: Key Responsibilities
Trial Master File Management
- Support TMF setup and maintenance for both hard copy and electronic systems
- Upload and maintain TMF files in Emerald Clinical's file-sharing system
- Serve as second reviewer for TMF quality control
- Assist with end-of-study TMF filing, QC, and archival processes
Site Start-Up Support
- Collaborate with CRA/CTM/PM during site start-up feasibility assessments
- Serve as point of contact for clinical sites during start-up phase
- Assist sites in preparing and collecting essential document packets (EDPs)
- Submit final EDPs to sponsors or project management teams
Quality & Compliance
- Perform quality control of documents and communications
- Develop skills in audit response preparation and participation
- Learn and apply ICH/GCP guidelines and regulatory requirements
- Support data entry for Clinical Trial Management Systems
Operational Support
- Assist with investigator payment tracking and submission
- Present feasibility results to project teams and sponsors
- Perform general administrative duties as required
- Continuously develop clinical research knowledge and skills
â Your Profile: Qualifications & Experience
Essential Requirements
- College/University degree OR 1+ year related experience OR equivalent combination
- Strong organizational and attention to detail skills
- Ability to perform administrative duties effectively
- Interest in clinical research and healthcare
Preferred Qualifications
- Exposure to medical terminology
- Knowledge of ICH/GCP guidelines and regulatory requirements
- Experience with document management systems
- Strong communication and collaboration skills
Professional Attributes
- Quick learner with adaptability to new systems and processes
- Quality-focused with meticulous attention to detail
- Team-oriented with excellent communication skills
- Commitment to professional development and learning
đŤ Why Join Emerald Clinical Trials?
Meaningful Work
- Contribute to life-changing clinical trials in critical therapeutic areas
- Support research that improves patient outcomes worldwide
- Work with a CRO that values both global standards and local expertise
Career Development
- Comprehensive training in clinical trial operations
- Clear pathway to advanced clinical research roles
- Exposure to diverse therapeutic areas and trial phases
- Mentorship from experienced clinical professionals
Competitive Benefits
- Tailored compensation and benefits package
- Opportunities for professional growth and development
- Employee wellbeing programs and work-life balance initiatives
- Global exposure with international project opportunities
⨠Ready to Start Your Clinical Research Journey?
If you're looking to begin a rewarding career in clinical research and have the foundational skills we're seeking, we encourage you to apply. We value potential and dedication - your willingness to learn and grow is what matters most!
Apply Now & Help Advance Global Healthcare
