Project Coordinator

Simbec-Orion; Merthyr Tydfil; On-site; GBP 27,000 - 38,000; Full time

Job summary

Simbec-Orion Group is seeking a Project Coordinator to join the Laboratory Services team. You will support clinical research projects from setup to completion, ensuring on-time delivery within budget and quality standards.

You will manage documentation, eTMF, study trackers and attend meetings, while coordinating lab supplies and global shipments for traceability. The role emphasizes strong organisation, attention to detail and ability to manage changing priorities, with opportunities to develop

Qualifications

• Bachelor-level qualification in Life Science or Business, or equivalent.

Responsibilities

• Support delivery of clinical research studies from set-up to completion.
• Prepare and maintain study documentation (LSP, SHM, eTMF) and maintain trackers.
• Attend project meetings and take minutes; identify risks and training needs.
• Manage supplies and logistics: dispatch lab supplies, monitor expiry, coordinate global shipments.
• Maintain shared study drive and ensure quality filing of correspondence.
• Organise sample shipments with full traceability.

Skills

Project management

Organisational skills

Time management

Microsoft Office

Teamwork

Education

BSc in Life Science or Business

Job description

Our Mission

Our passion for improving patients’ lives motivates us to apply our skills, experience and knowledge to advance medicine.

We achieve this through flexible, innovative, high-quality solutions for our clients, delivered with integrity.

The Role

We are looking for a Project Coordinator to join our Laboratory Services team, supporting the delivery of clinical research studies from set-up through to completion.

Working closely with the laboratory study team, you will help ensure projects are delivered on time, within budget and to the agreed quality standards. You will prepare and maintain key study documentation, including Laboratory Service Plans, Sample Handling Manuals and the electronic Trial Master File, keep study trackers up to date, and support clients and stakeholders by attending project meetings and taking minutes. You will also help identify study risks and develop study-specific training for the team.

Alongside this, you will run our supplies and logistics service. As the first point of contact for supply and shipment requests, you will prepare and dispatch laboratory supplies to investigator sites, monitor expiry dates and coordinate the global shipment of supplies and samples with full traceability.

This is an excellent opportunity for a life science or business graduate looking to build a career in clinical project management. Previous laboratory or clinical research experience would be an advantage, but strong organisation, attention to detail and the ability to manage changing priorities matter most.

Key Accountabilities

• Work with the laboratory study team, under general direction, to ensure assigned projects are delivered within scope and budget and meet agreed deliverables and quality expectations.
• Assist in keeping clients and stakeholders informed of project progress, including attending meetings and taking minutes.
• Assist in identifying potential laboratory study risks and support risk management throughout the project.
• Monitor and maintain project-specific laboratory training, including developing and presenting study-specific training and meeting materials, and maintaining attendance logs and reading lists.
• Maintain study trackers, such as the Sample Management Tracker for external studies, where applicable.
• Assist in preparing and executing the laboratory documentation required for each project, including but not limited to the Laboratory Service Plan (LSP), Sample Handling Manual (SHM), external Test Request Forms (TRFs) and manifests, and the clinical trial logistics strategy.
• Maintain the shared study drive, the electronic Trial Master File (eTMF) and laboratory study files from set-up to archive, including uploading and quality checking laboratory documentation and filing key correspondence, as applicable.
• Prepare and dispatch laboratory supplies to investigator sites in line with clinical study protocols.
• Monitor supply expiry dates and ensure the expiry dates of consumables held at investigator sites are accurately logged.
• Organise study sample shipments, ensuring full traceability throughout.

Skills Required

ESSENTIAL

• BSc in a Life Science or Business discipline, or equivalent
• Knowledge of basic project management principles
• Excellent organisational and time management skills
• Ability to work to deadlines and manage changing priorities
• Working knowledge of Microsoft Office, including Word, Excel and PowerPoint
• Ability to work effectively as part of a team

DESIRABLE

• Formal project management qualification or certification
• Experience working in a laboratory environment
• Experience working in clinical research
• Experience managing multiple projects concurrently
• Awareness of Good Clinical Practice (GCP)
• Experience with quality control procedures
• Project management experience in a laboratory or clinical research setting

About Us

Simbec-Orion is a responsive and agile full-service CRO, delivering studies from first in man through to Phase III. Our experts leverage wide therapeutic experience and specialist expertise to execute a comprehensive portfolio of trials. We are perfectly structured to provide full-service clinical development solutions for small and mid-size drug developers, headed up by a centralised leadership team.

With a focus on tailormade and scalable solutions, we adapt our delivery style, communications and operations to suit the demands of the project, helping clients achieve their clinical and commercial objectives. Because our goal is the same as theirs; to improve patients’ lives.