RESPONSIBILITIES

* Perform complex processes and tasks that eventually result in high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines
* Establish and maintain effective project/ site communications
* Create and maintain relevant project documents
* Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information
* Participate in document management (creation, review, maintenance, storage, as applicable

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

* Good knowledge of applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines
* Strong written and verbal communication skills including good command of English language
* Results and detail-oriented approach to work delivery and output
* Good problem solving skills
* Good planning, time management and prioritization skills
* Attention to detail and accuracy in work
* Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint
* Ability to establish and maintain effective working relationships with coworkers, managers and clients.
* Proven ability to work on multiple projects balancing competing priorities
* Ability to coach/ mentor junior colleagues