Clinical Project Coordinator

Alimentiv; Waltham Cross; Remote; GBP 34,000 - 52,000; Full time

Job summary

Alimentiv is seeking a Clinical Project Coordinator to provide administrative and project support across clinical studies from a home-based setting. You will help with document development, testing, tracking, and scheduling meetings, training, and communications with sponsors and sites.

The role emphasizes quality, regulatory compliance, and cross-functional collaboration, with responsibilities including invoicing support, document control, and acting as the first point of contact for project

Qualifications

• Minimum 1–3 years of related work experience with ongoing training, or at least a 1-year college diploma/degree in health, life sciences or clinical research.
• Knowledge of clinical research, ability to work independently, strong communication skills and cross-functional collaboration.

Responsibilities

• Coordinate meetings, agendas, minutes and project communications.
• Assist with document/process/report development, testing, tracking and management.
• Support invoicing and billing documents and project communications throughout the life cycle.
• Provide administrative support, logs, reports and scripts for project life cycle.
• Act as first point of contact for project queries and issue escalation.

Skills

Clinical research knowledge

Independent work

Strong communication skills

Cross-functional team work

Education

College Advance Diploma/Degree in Life Sciences or Clinical Research

Job description

Clinical Project Coordinator

Provide administrative, clerical, implementation and/or processing support to the project teams and stakeholders. Assist with document/process/report development, testing, tracking, distribution, and management. Coordinate meetings, presentations, and training activities, facilitate billing and payment activities, and act as first point of contact for project queries. Ensure that all activities align with quality standards, project guidelines, corporate best practices, and regulatory standards and guidelines.

Project Support

• Prepare and coordinate flow of documents, materials, and resources for project meetings and presentations, preparing meeting agendas, minutes and documents, scheduling and coordinating project committees, sponsor and site meetings, and tracking training programs and activities
• Facilitate project invoicing, billing and payment document preparation including support documents, and assist with internal and external communications throughout the project life cycle.

Document Management

• Assist team, providing timely administrative support, including form preparation, client/project information entry, creating logs, reports, and scripts
• Contribute to the creation and maintenance of project forms, documents and processes during the project life cycle and assist with project issue identification and resolution during audits that is consistent with project requirements.

Client/Sponsor Support

• Act as first point of contact for project queries, appropriately identifying, addressing, redirecting or escalating questions, protocol clarification requests and project/service issues appropriately, that are consistent with project requirements, regulatory standards and corporate code of conduct.

Document Control

• Manage and maintain project materials, tools, equipment and supplies, ensuring all activity is entered/recorded, distributed, tracked, monitored, updated, revised and/or maintained in accordance with project protocols, industry best practices and regulatory standards and guidelines.

Qualifications

• Applicants should have a minimum of one to three years of related work experience with ongoing training, or a minimum of a one-year College Advance Diploma/Degree in a relevant field of study, preferable in Health or Life Sciences, or Clinical Research. The successful candidate must exhibit the following skills: Knowledge of clinical research, ability to work independently, strong communication skills, and the ability to work in a cross‑functional environment.

Working conditions

• Home Based
• *Accommodations for job applicants with disabilities are available upon request