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Clinical Research Project Coordinator
hace 1 semana
Company Overview
">At ICON, we are a world-leading healthcare intelligence and clinical research organization. Our mission is to shape the future of clinical development, and we're proud to foster an inclusive environment driving innovation and excellence.
">Job Summary
">We are seeking a highly motivated Clinical Research Project Coordinator to join our team in Mexico City. This is a challenging role that requires strong organizational skills, attention to detail, and excellent communication abilities.
">Key Responsibilities:
">- ">
- Manage projects in a timely manner in adherence with ICON's SOPs, ICH, GCP, and appropriate regulations">
- Delivery of projects in accordance with the contract, timelines, and study budget">
- Identification and review of change orders for the budget">
- Attend and present at client investigator, kick-off, and client meetings">
- Ensure all necessary study-specific training is provided to the study team to improve performance and knowledge">
- Management of eCRF development process">
- Development/Review/Maintenance of all trial documentation (Charter, eCRF, SRS, Reviewer Training Manuals)">
- User Acceptance Training and demonstration of eCRF">
- Data reconciliation">
- Primary client and CRO contact; develops successful working relationships with client/CRO">
- Preparation and management of meeting agendas and minutes">
- Prepare/Approve Project Reports">
- Management of Study Centers">
- Coordinates readers and review sessions">
- Conducts reader training with support of Project Director">
- Monitors Offsite Assessments/Blinded Reads">
- Quality Control of Offsite Assessments/Blinded Reads">
- Ensures all management/tracking systems are up-to-date">
- Provide regular feedback to senior management on project status, client satisfaction, and staffing issues">
- Manages Data Management Lead for scheduling and preparation of data deliveries as required">
- Participate in BD activities as appropriate">
- Supports internal, client, and regulatory audits">
- Ability and willingness to travel">
- Participate in interviews as required">
Requirements:
">To be considered for this role, you will need to have a minimum of a bachelor's degree (preference in Life Sciences or similar) or equivalent education/work experience.
">You should also have relevant work experience in timeline management and previous experience in a project management role within the clinical trial industry.
">Advanced English fluency is required for business communication.
">What We Offer:
">We offer very competitive salary packages, including an estimated annual salary of $120,000 - $150,000 depending on experience.
">In addition to a competitive salary, we provide a range of health-related benefits to employees and their families, including comprehensive health insurance and retirement plans.
">We also offer opportunities for professional growth and development, as well as a dynamic and supportive work environment.
">Equal Opportunities Employer:
">ICON is an equal opportunity and inclusive employer committed to providing a workplace free of discrimination and harassment.