Your new employer is Covance by Labcorp, the world's most comprehensive drug development company, dedicated to improving health and improving lives.Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of drug development data in the world, along with our innovative technology solutions, help our clients identify new approaches and anticipate tomorrow's challenges as they evolve. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.

This is your chance to become part of a team that helps to bring the miracles of medicine to market sooner. Excellent opportunity for a Project Coordinatorto join our Phase I Clinical Research business in Leeds, West Yorkshire on a full-time and permanent basis. This is a great opportunity to develop your career within Clinical research/trials and allow you to continue to practice your clinical skills and knowledge. You will be supporting Project Manager focusedon early phase studies.

Key Responsibilities

Your main responsibilities will include but not be restricted to:

• Works independently with little assistance from a more senior PC or PM in owning and developing study specific documents (e.g., Project Management Plan, Communication Plan, Investigator Package Plan, Risk Register, Project Specific Training Matrix and any other applicable plans as required), including compliance with client-specific requirements, for low to medium complex studies including external site studies. Distributes them to the study team and/or sponsor for review, compiles comments, makes updates with minimal assistance and routes final documents. Proactively monitors training compliance of the study team and updates the training matrix as required.
• Maintains an internal standardized filing structure for study related documents; proactively maintains documents within the filing structure, and suggests changes as necessary to maintain organized files.
• Responsible for project setup activities (e.g., study ID request, SAS Environment Setup request, eTMF, Study-specific Distribution Lists, etc.).
• Manages the setup and updating of CTMS. Attains local country project expertise for CTMS reporting, study metrics, risk management regarding communication, coordination and eTMF quality.
• Independently organizes and attends applicable study-related meetings; generates and distributes agendas, maintains and distributes meeting minutes, works with the PM to set up and maintain the Project Log, Risk Register, and study team contact lists; monitors/takes action on follow-up items from meetings; may facilitate routine update meetings including external site meetings in the absence of the PM, if needed; reviews documents for completeness and quality to reduce PM review time; participates in client visits as needed.
• Routinely posts documents such as CRA reports, project deliverables, trackers, regulatory documents, metrics, agendas, and minutes to internal SharePoint site/client websites after completing administrator and program training on the required system.
• Independently participates in business improvements initiatives as assigned to drive quality, productivity, and continuous improvements across different business units; develops new ideas for improvement initiatives within own business unit.

Get ready to redefine what's possible and discover your extraordinary potential at Covance by Labcorp. Here, you'll have the opportunity to personally advance healthcare and make a difference in peoples' lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you'll be empowered to own your career journey with mentoring, training and personalized development planning.

Join us and discover why Covance by Labcorp has been named by Forbes as one of the World's Best Employers 2020 and more than 90% of the top 20 global pharmaceutical companies are repeat customers. We can offer you not only a job, but a stable, long-term international career.
Education/Qualifications:

• University/college degree, preferably in a healthcare/scientific field. Specific clinical research experience may be substituted for education.

Experience:

• Knowledge of the clinical trial process with early clinical pharmacology experience preferred.
• Recent and relevant experience in a clinical research environment.
• Experience working in a project management environment. Knowledge of protocol designs, study objectives, study procedures, and project-related timelines.
• Knowledge of GCP/ICH Guidelines and applicable Regulatory Authority Guidelines.

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