• Manage enquires and organise appointments received to the Private Clinic, including working with embassies, international private customers travelling, insurance companies and the medico-legal industry
• Produce comprehensive medico-legal reports for insurance companies
• Manage, motivate and coach a small team
• Strategic and business development planning, including sales forecasting, data analysis, improving overall sales and profit performance, providing relevant reports and recommendations for action
• Assess market/industry competition with ongoing competitor analysis and research. 
• Keep up to date with industry trends
• Maintain a robust sales cycle, including quotations, contracts and payments, ensuring pricing is in line with company expectations on margin and patient fairness.
• Act as a resource to hospital and agency personnel providing education on the care, treatments and services that are available for provision in the home setting.
• Maintains knowledge of insurance and reimbursement guidelines and changes. 
• Understands and utilizes Medicare home care guidelines in establishing home care referrals.
• Coordinates the home care plan and assures that services are available as ordered by physician.
• Documents patient’s home care plan and coordinates activities according to standards established by LTC and by the hospital or agency

• Sgn post staff and family members to relevant information on living with Dementia
• Work alongside the Registered Manager and Deputy Manager to make sure that the rota is completed and constantly updated to make sure home is fully staffed at all times
• Assist in making sure that company Policies and Procedures are being followed in the home at all times
• Liaising with external stake holders, this includes Social Worker's, GP's and Families.
• Act as a positive role to all junior and less experienced staff
• Assist activity staff in thinking of suitable activities to do in and around Leicestershire
• Work with the Registered Manager and complete all HR paper for all staff
• Assist the activities team and looking for suitable activities for all residents to take part in based in Leicestershire and the surrounding region
• Assisting the Registered Manager to complete the staffing rota to make sure the home as the correct staffing ratios at all times
• Conduct and complete audits on the medication onsite to make sure the stock levels are all correct
• Assist in completing initial assessments on new residents
• Complete Care plans on each resident and make sure that are kept updated and relevant
• Assist the activities team in looking for new activities to be completed in-house or out in the wider community Leeds based or further away

• Ensure quality of the clinical monitoring and site management deliverables within a project and maintain proper visibility of its progress by the use of approved systems and / or tracking tools.
• Interact with the client and other functional departments related to clinical monitoring and site management activities and deliverables.
• Maintain thorough knowledge of applicable Amarex SOPs, guidelines and written study procedures for the project.
• Assist with protocol and Case Report Form (CRF) review/writing by the project team.
• Develop and/or review Informed Consent Form (ICF) template.
• Manage site start-up procedures, including site identification, feasibility questionnaire assessment, Institutional Review Board (IRB) submissions, contract/budget negotiations, direct monitoring activities and assist with site start-up questions.
• Oversee collection and review of required regulatory documents.
• Develop, implement and monitor compliance with the study monitoring plan.
• Develop clinical monitoring strategies to assure study timelines are met.
• Assist with the development of study manuals, tracking forms, study site tools, and other study materials.

• Assist with investigator meeting activities including organization, preparation, and attendance.
• Serve as back-up to the Project Manager (PM).
• Coordinate timely shipment of clinical supplies and Investigational Product to sites according to the study-specific procedures.
• Establish and maintain adequate site tracking records in terms of subject enrollment/randomization, monitoring visits, investigator payments, and any other items related to site management, as appropriate to the project.
• Follow up of safety issues and safety reports in timely manner, as requested by the Safety and Pharmacovigilance Department.
• Communicate site study issues, concerns, and progress to the PM and Sponsor’s management team, as specified in the Project Management Plan.
• Assist with the implementation of corrective actions related to clinical study site management and monitoring, as necessary.
• Participate in routine study progress meetings, face to face or via teleconference.
• Promote the establishment of routine contact and maintenance of good rapport between the assigned CRA and the study sites.
• Ensure periodic updates are obtained from CRAs and provided to the PM and/or Sponsor team
• Maintain frequent communication with CRAs, providing guidance as necessary and in agreement with monitoring plan.

• Review and approve expense reports for CRA visits, if requested by the PM.
• Establish and maintain clinical monitoring tracking tools, study tools and study templates for site personnel, with appropriate guidance and instructions
• Develop study-specific training materials for CRAs.
• Manage CRA training such as track and maintain documentation of CRA training throughout the life of the project.
• Track the compliance of CRA visit frequency and other tasks (per the approved monitoring plan) throughout the study.
• Promptly escalate CRA non-compliance to the PM.
• Alert CRAs to potential issues (e.g., data management query trends, missing CRF pages, outstanding monitoring reports, etc.).
• Perform site visit activities (e.g., site qualification visit, site initiation visits, site training, site routine monitoring visit, site closeout visits, etc.) for training/retraining or as back-up to an assigned CRA.
• Assist with the monitoring of difficult sites that may be too challenging for a less experienced CRA.
• Work with the Project Team to ensure that all other activities related to the clinical sites and monitoring for the clinical trial are accomplished.

• Current or recent experience of working in a patient-facing, clinical role within a mental health service.
• Experience as IAPT Practitioners, CBT Therapists, Mental Health Practitioners, Child or Adult Mental Health Nurses, Clinical Psychologists, Psychiatrists and equivalents.
• Demonstrable written and verbal communication skills
• The ability to work well within a team and individually, using initiative and autonomy
• Solid organisational skills including attention to detail
• Problem-solving skills, with the ability to be flexible in approach to work
• A committed work ethic, with enthusiasm to develop skills and a drive to learn
• The ability to work in a fast-paced environment
• The ability to adapt to changes in the work environment
• A high standard of professionalism
• Demonstrable experience in quality improvement, digital health, education and/or clinical research would be advantageous
• Experience working both in community and secondary mental health services

Qualifications: BS in Nursing with 5 years of experience

• Experience as a CRA, CL or PM (onsite monitoring or remote monitoring experience)
• Working knowledge of clinical financials including understanding of budgets, pass- through and resource management
• Strong knowledge of ICH / GCP regulations
• Advanced knowledge of FDA Guidance Documents / EU Directives / ISO14155 regulations, drug/device development, and clinical monitoring procedures
• Strong knowledge of web-based communication tools, and MS Office computer skills
• Fluent verbal and written English as well as the local language
• Known for being customer-focused in approach to work and communications with the ability to professionally interact with sites, clients, vendors and other functional areas
• Strong verbal and written communication and negotiation skills
• Maintains a positive, results-orientated work environment
• Excellent team player, collaborative and able to build an effective team
• Strong people management skills to motivate, enthuse, and lead
• Excellent organizational and time-management skills, able to prioritize work to meet deadlines
• Ability to multitask and work effectively in a fast-paced environment with changing priorities, accountability, dependability and strong commitment.

Qualifications: BA in Health Administration with 4 years of experience

• Expert in MSK, with experience in Vocational Rehab, Pain or Concussion
• Client-centric with genuine empathy for clients
• Keen to be part of bigger picture clinical care wrapping services around clients for the best outcome
• Ability to work autonomously and within a team
• Have a growth mindset
• Top performer who is motivated and ambitious, with a knack for business development
• Proven relationship-building and networking skills
• Strong desire to learn and be a contributing member of a wider MDT
• Experience with a specialization in oncology (e.g., as a medical oncologist, oncology nurse)
• Worked in a research environment either as a principal investigator or member of a research team in academic or industry context
• Interest and experience with creating databases for research

Qualifications: BS in Biomedical Science with 3 years of experience

• RGN or RMN qualification with an active NMC pin,
• A proven track record of leading a nursing team in the delivery of person-centred care/ including planning/ implementing and evaluating,
• Experience of delivering quality clinical and person-first assessments,
• The ability to engage with the service users to understand needs in order to provide an excellent service of person centred care,
• Good working knowledge of CQC standards,
• Promote ownership of care programs by fully involving service users and families in developing/ agreeing and evaluating care programs within the home,
• Confidence to communicate and maintain excellent working relationships with all levels of colleagues/ internal as well as external professionals/ families and visitors.
• Experience with health records, and electronic clinical systems
• Experience with how clinical data are represented (e.g., understanding of ICD codes
• Excited about working in a passionate, fast-paced, technology-driven culture
• Experience in collaborating and easily explaining scientific terms to a non-medical, highly sophisticated audience and  superior communication skills

Qualifications: BA in Psychology with 5 years of experience

• Have experience managing an Endoscopy unit
• Experience in implementing changes to improve the service
• Experience in supporting staff flexibly to run the service efficiently
• Work with the theatre manager to look at new ways of working across the two departments to enhance the staff and patient experience.
• Experience in Engaging with Consultants to improve the utilization of the unit.
• Experienced clinician with the evidenced capacity to effectively operate at a comparable level and work collaboratively within a team of multi-disciplinary health professionals.
• Knowledge and experience in working within regulatory and legislative practice parameters in relation to nursing practice and have a developed understanding of the Aged Care Quality Standards, in order to meet the clinical compliance requirements of the role.
• Current National Crime Check (or capacity to obtain)
• Experience in management and healthcare 
• Experience and expertise with Microsoft Office (Word, Teams, PowerPoint, Excel)
• Demonstrated ability to utilize and execute administrative systems and processes consistently and proficiently to contribute to operational success
• Excellent communication skills with all levels and among team leaders

Qualifications: BA in Public Health with 4 years of experience