**Clinical Trial Coordinator Role Overview**
We are seeking an experienced and highly motivated Clinical Trial Coordinator to join our team. The successful candidate will be responsible for supporting the planning, execution, and monitoring of clinical trials.
Responsibilities:
* Communicate and collaborate with global study teams, working closely with project coordinators and managers;
* Ensure timely delivery of tasks with a high degree of accuracy;
* Compile and maintain project-specific status reports within the clinical trial management system;
* Interact with internal project teams, sponsors, study sites, and third-party vendors;
* Provide oversight and quality control of internal regulatory filing systems;
* Manage study supplies and create project timelines;
* Coordinate project meetings and produce quality minutes.
Qualifications:
* PhD in Life Sciences or relevant field;
* Experience in Cardiovascular, Renal & Metabolic Disease (CVRM) preferred;
* Fluency in English with excellent presentation skills;
* Ability to work in a fast-paced dynamic industry within an international team;
* Prior experience within the CRO or pharmaceutical industry advantageous but not required;
* Excellent computer skills, organisational, and communication skills.
Benefits:
* Competitive compensation and benefits package;
* Flexible work environment;
* Structured career paths with opportunities for professional growth;
* Company-sponsored employee appreciation events;
* Employee health and wellness initiatives.
About Us:
We are a leading contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach.
Join Our Team: