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Patient Engagement Manager
Central London - Site Based
From £31,000
Full-time, 40 Hours, Mon-Fri, 10:30am to 7:30pm

THE OPPORTUNITY

An exciting opportunity has arisen for a driven and organised Patient Engagement Manager to join our client's well-established and growing healthcare practice in Central London click apply for full job details

About Us

Complex Care Professionals Ltd is a growing, forward-thinking organisation with branches across the North West. We are committed toputting people firstboth our clients and our staff.

Were looking for an organised and proactiveCare Coordinatorto support the delivery of high-quality, person-centred care while helping to grow and develop our services click apply for full job details

Job Description

Are you looking for a rewarding role in a trusted care company? At Altogether Care, our family values ensure that we put people first.

Join us as a Care Coordinator and become part of our growing family. Enjoy the support of great teams and consistent working hours click apply for full job details

Talentmark are recruiting for a Logistics Coordinator to join a rapidly growing organisation within the life sciences and clinical trials sector at their site based in Burton on a full time, permanent basis. The role will be hybrid-based, with 2 days a week in the office, for a salary of 30,000 per annum.

The Company:
Our client are a Pharmaceutical Services company who work on supplying and sourcing medicines for clinical trials; they have a global presence and are headquartered in Burton-upon-Trent.

Location:
The Logistics Coordinator will be based at the company's site in Burton-upon-Trent, easily commutable from Derby, Lichfield, Uttoxeter, Walsall, Nottingham and Stoke.

Logistics Coordinator Role:
Reporting to the Director of Operations, this role will involve managing paperwork, warehouse deliveries and shipment arrangements, ensuring work is carried out strictly according to Good Distribution Practice.

Your main duties will include:

• Arranging inbound shipments for supplier and warehouse requirements.
• Generation of documentation and management of inbound activities.
• Working to warehouse SOPs to schedule, arrange and manage inbound and outbound shipments.
• Ensuring effective stock inventory management.
• Monitoring shipments and escalating delays as required.
• Supporting with QA, DSCSA and FMD activities.

• 1-2 years' prior experience within the healthcare/pharmaceutical logistics sector, with GDP (Good Distribution Practice) exposure.
• Commercial awareness is required.
• Excellent and clear communication skills at all seniority levels.
• Comfortable with multi-tasking and prioritising within a fast-moving environment.

About Us

Complex Care Professionals Ltd is a growing, forward-thinking organisation with branches across the North West. We are committed to putting people first both our clients and our staff.

Were looking for an organised and proactive Care Coordinator to support the delivery of high-quality, person-centred care while helping to grow and develop our services click apply for full job details

Care Coordinator Domiciliary Care
Andover
Competitive Salary + on call payments
Company: Nurseplus

Are you an organised and compassionate individual with a passion for delivering high-quality care? Do you thrive in a fast-paced environment where no two days are the same? If so, Nurseplus has an exciting opportunity for you.

We are looking for a dedicated Care Coordinator to join our Andover branch, supporting the delivery of exceptional domiciliary care services. This is a key role within the branch, ensuring the smooth coordination of care staff and services to meet client needs.

As a Care Coordinator, you will be responsible for managing staff rotas, coordinating care packages, and ensuring the highest standards of service delivery.

Key Responsibilities:

• Scheduling and coordinating care staff to meet client requirements

• Managing and updating rotas, ensuring efficient staff utilisation

• Building strong relationships with care staff, clients, and their families

• Supporting the onboarding of new care workers, including compliance checks

• Responding to last-minute changes, sickness, and emergency cover

• Ensuring care delivery meets regulatory and company standards

• Working closely with the recruitment team to maintain staffing levels

• Maintaining accurate records and using internal systems effectively

We are looking for someone who is highly organised, proactive, and able to work under pressure.

Requirements:

• Previous experience in a care coordination, scheduling, or similar role is desirable

• Experience within domiciliary care or healthcare is advantageous

• Strong organisational and time-management skills

• Excellent communication and interpersonal abilities

• Ability to problem-solve and respond quickly to changing situations

• A calm and professional approach in a fast-paced environment

• IT literate and confident using scheduling systems

• A full UK driving licence is preferred

• Competitive salary

• Bonus opportunities

• Ongoing training and development

• Clear career progression pathways

• Supportive and friendly team environment

• Company pension scheme and employee benefits

• The opportunity to make a real difference in people s lives

Nurseplus is a leading provider of healthcare staffing and domiciliary care services across the UK. We are committed to delivering high-quality, person-centred care and supporting our staff to achieve their full potential.

Apply today and be part of a team that makes a difference every day.

INDPRM

Care Coordinator - £29,973.84 + Benefits- Ellesmere Port & Chester

The Role

Are you experienced in care coordination and confident managing rotas, care plans and support teams? Do you enjoy making a real difference while helping people maintain their independence and quality of life at home? If so, we'd love to hear from you click apply for full job details

Housing Management Coordinator

Pay £14.06 per hour (£27,500 per annum) and great benefits including Health Cash Plan

Permanent, full time (37.5hpw)

Penzance will be your main base, but the role also covers the Redruth area.

Home, a place where you belong

This is a great opportunity to join our team click apply for full job details

Talentmark are recruiting for a Lab Support Coordinator to join a company in the diagnostics industry on a contract basis for 12 months.

Salary:
Paying 200- 230 per day PAYE, or 265- 305 Umbrella.

Lab Support Coordinator Role:

• User support functions: including installation and support on our systems.
• customer training.
• troubleshooting, sales and customer support.
• software modifications and product maintenance.
• assistance with tender responses and product demonstrations.

• Biochemistry / pathology background.
• Thorough understanding of IVD industry.
• Have experience of support of pathology lab solutions.
• Troubleshooting / technical service cover for lab instruments - mostly biochemistry.
• Excellent customer facing skills.

Role of CLINICAL TRIALS COORDINATOR involves working alongside a well -known professor and the Lead Clinical Trials Coordinator coordinating and managing the research trials and projects. It is a role that will straddle both the Clinical Trials and Research Department. The salary depends on experience, it s up to £45k.

The role requires prior commercial experience, and we politely ask candidates without this experience not to apply.

The Clinical Trials Coordinator will be expected to assist with organising, initiating and carrying out multiple funded and not industry-sponsored data collection and research projects in one or more of the following areas, amongst others: Early, Intermediate, Late (Dry and Wet) Age-Related Macular Degeneration including Gene Therapy as a treatment option, amongst others; Wide-Field OCT and Imaging of the Peripheral Vitreoretinal Interface; Diabetic Macular Oedema; Inherited Retinal Dystrophies; Visual Aids; Vitreous Floaters and Opacities.
The Clinical Trials Coordinator will assist with analysing and writing up academic papers which are then sent for publication

The clinic focuses on developing research in Medical Retina and Vitreoretinal conditions using the most advanced diagnostic and treatment devices in order to offer the best options for clinical care and to improve patient health. The Clinic is equipped with the latest diagnostic and research resources including Optomap digital wide- field multispectral imaging, Microperimetry, 3D Fourier-Domain as well as the new Infra-Red Swept Source DRI Cross-Sectional OCT, En-Face OCT, OCT angiography, Yellow Pascal subthreshold laser with Endpoint Management, YAG laser for Vitreolysis and Photo-Biomodulation, amongst others.

The Clinical Trials Coordinator duties:
• Ensure regulatory and professional standards of clinical trials are achieved and maintained at all times
• Adhere to strict clinical trial timelines
• Collect data including diagnostic imaging where appropriate
• Provide regular updates to the Principal Investigators
• Maintain clinical trial and patient records according to study protocol and that the trials are conducted in accordance with Good Clinical Practice guidelines
• Assist in setting up new projects, attend annual scientific ophthalmic meetings (if appropriate) and produce the required study reports and scientific publications
• Corresponding with study patients
• Prepare lectures and assist in creating material for publication (scientific and promotional).
• Ensure all payments throughout the study are paid and tracked efficiently
• Respond to all PR enquiries with an urgent manner
• Analyze project data and communicate complex results clearly to the research team and study Sponsor
• Assist in writing up research findings, supporting research staff, for publication in journals and for submission to national and international conferences
• Monitor performance of the research trials/projects and be responsible for deadlines, occasionally working out of hours to ensure deadlines are met
• Respond and coordinate all PR related activities with an urgent manner as these tasks tend to have a very tight deadline on them
Requirements for the role
We are also looking for a previous clinical trials coordinator experience (around 2 years), preferably coming from a private sector. Ophthalmology is preferred but not mandatory.
The ability to work with large databases
The ability to communicate and interact effectively, calmly and compassionately, during various points of contact with patients and staff alike

DUTIES - DAILY
• Daily management of prospective studies, including patient follow-up, testing protocols, data entry, patient examination
• Liaising with the lead trials to ensure that all tasks are completed and providing regular updates on the study progression
• Contacting patients to schedule appointments and follow ups
• Scanning and examining study and clinical patients
• Assisting with treatments in the operating room
• Working on data collection for research projects where necessary including: producing and analysing databases; ensuring that the correct data is being collected in clinic.
• Assisting with the writing up of academic papers based upon research conducted in the clinic
• Dealing with administrative duties

Shifts: 8.00am-5.00pm, 9.00am-6.00pm, 10.00am-7.00pm