In this position, you will be a vital bridge between our clinical, governance, safeguarding, and patient-care teams, and will act as one of our organisational Safeguarding Leads. You will be responsible for the caseload of complex mental health patients and involved in follow-up of these patients while also serving as the internal subject matter expert for complex mental health presentations. Your expertise will guide the wider team and ensure our clinical governance frameworks meet the highest standards of safety. What you will be doing Complex Caseload & Longitudinal Management: - Specialist Follow-up Care: Regular review of the management of a dedicated caseload of patients who are already under a mental health team or where this is required. Specifically patients with escalating or intricate needs, ensuring their long-term treatment plans remain safe and effective. - External Clinical Liaison: Act as the key point of contact for external GPs or NHS Mental Health Services where required; facilitating a joined-up approach to patient care and ensuring robust information sharing to maintain patient safety. - Complex Clinical Reviews: Conduct deep-dive reviews for cases referred to you whose presentation or medical history requires a higher level of clinical scrutiny than routine follow-up. - Stabilisation & Escalation: Act as the primary point of intervention for clinical escalation, providing expert advice to patients and staff when a case moves beyond routine care or requires specialist adjustment for complex mental health patients. Clinical Governance, Safeguarding & Leadership: - Clinical Leader: Act as a primary source of expert advice for all clinicians across the organisation, offering guidance on complex mental health queries and best practices as well as training the wider clinical team in this field. - Governance Integration: Work as a key link between the frontline clinical team and the Governance Team, reviewing clinical incidents and refining screening protocols to align with clinical, professional and regulatory standards. - Safeguarding Lead: Drive organisational safeguarding excellence through oversight of clinical governance frameworks, policy development, delivery of mandatory safeguarding training, leading complex safeguarding investigations, conducting regular audits, and providing specialist safeguarding supervision to the clinical team. - MDT Subject Matter Expert: Provide authoritative guidance to the Multi-Disciplinary Team (MDT) regarding complex mental health cases and the safe application of CBPMs. - Protocol Development: Use specialist insights to help refine mental health screening protocols and risk management frameworks What do you need? - NMC Registered: RMN (Registered Mental Health Nurse) status is essential. - Experience: A minimum of 5 years’ clinical experience, with a focus on mental health care, complex risk assessment, and longitudinal case management. - Safeguarding & Governance Expertise: Proven experience in clinical auditing, risk management, or safeguarding lead responsibilities within a healthcare setting. - Specialist Knowledge: A robust understanding of mental health medications, dual diagnosis, and the long term management of complex mental health patients. - Remote Proficiency: Confidence in using digital platforms for video consultations and maintaining accurate electronic patient records. - Communication: Exceptional organisational skills and a compassionate, patient-centred approach to managing complex clinical narratives. What we offer: - Generous Leave: 25 days holiday (rising to 27 after year one and 30 after year two) + 8 bank holidays - Pension Matching: Up to 5% employer matching contributions - Flexibility and Wellness: Work-from-home options, cycle-to-work scheme, and more - Growth Opportunities: Collaborate across teams and represent Montu at events, with support to grow your skills and impact - Enhanced Maternity & Paternity Leave About Us Montu UK is a leading digital health company specialising in cannabis-based medicines (CBPM), dedicated to improving patient access to safe and effective treatments. Our mission is to transform lives by combining innovative technology with high-quality clinical care, ensuring patients receive the support they need at every step of their journey. As a fast-growing organisation, we offer a collaborative and supportive environment where talented people can develop their careers while contributing to meaningful change in healthcare. At Montu UK, your work has a direct impact on improving patients’ lives and expanding access to modern medical treatments.

Company Description PSI is a leading Contract Research Organisation with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. Your focus will be on subjects’ rights, safety and well-being and quality of data compliance. This is a freelance (contractor) home-based position in Slovakia. Your responsibilities will include: - Conducting and reporting all types of onsite monitoring visits - Driving the study startup phase (if applicable) - Performing CRF reviews, source document verification and query resolution - Be responsible for site communication and management - Supervising study activities, timelines, and schedules for each site - Acting as a point of contact for in-house support services and vendors - Supporting quality control, such as compliance monitoring and reports review - Participating in feasibility research - Supporting the regulatory team in preparing documents for study submissions and regulatory approval Qualifications - BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience - Independent on-site monitoring experience in Slovakia, ideally on multiple projects at a time - Demonstrable experience in all types of monitoring visits in Phase II and/or III - Full and clean driver's license, and the ability to travel. - Fluency in Slovak and English - Experience supporting Oncology studies is beneficial, but not essential - Intermediate to Advanced knowledge of MS Office Additional Information Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way. We will guide and support you with information, making your experience as smooth as possible.

Job Description Summary As an Application Specialist, you’ll be the clinical and technical expert who empowers healthcare professionals and drives innovation in surgical imaging. Your mission? Deliver exceptional support, inspire confidence, and help shape the future of Surgical Visualization and Guidance (SVG) in the UK market. You will report to the Lead Clinical Applications & Sales Specialist and will provide coverage across the UK, with a primary focus on the South East and London region; regular travel will be an essential part of the role. Job Description Responsibilities Be the Expert: - Provide hands-on, remote, and phone-based support to customers and colleagues, ensuring seamless integration of our solutions into clinical environments. - Deliver high-impact demonstrations and training sessions—both in-person and online—that showcase the power of ultrasound in surgical care. - Partner with clinicians in operating theatres to elevate patient outcomes through advanced imaging solutions. Lead the Way: - Organize and execute exhibitions, workshops, and courses that position SVG as a market leader. - Build strong relationships with decision-makers and influencers, becoming a trusted advisor in their purchasing journey. - Identify and nurture Key Opinion Leaders (KOLs) to strengthen our clinical network and brand reputation. Drive Growth: - Monitor market trends, report insights, and take proactive steps to keep SVG ahead of the curve. - Collaborate with internal teams to remove barriers, improve processes, and accelerate business growth. Your Impact - Deliver world-class training and support that clinicians value and trust. - Contribute to a strong, united team shaping the UK clinical strategy. - Enhance SVG’s image and brand awareness through excellence and innovation. Desired Characteristics - Basic experience in medical devices, ideally with ultrasound or imaging technologies. - Strong clinical and product knowledge, plus proficiency in Microsoft Office. - Exceptional communication skills, a proactive mindset, and the ability to thrive under pressure. - A dynamic, self-starting attitude with flexibility to adapt quickly. - Willingness to travel Why This Role Matters - You’re not just supporting customers—you’re transforming surgical care. By combining technical expertise with clinical insight, you’ll help clinicians deliver better outcomes and position SVG as the go-to partner for innovation. Inclusion and Diversity GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. Behaviors We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity. Total Rewards Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support. #LI-BG1 #LI-remote Additional Information Relocation Assistance Provided: No

Clinical Trial Manager / Local Study Manager Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health - We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. - We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. - We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. Job Responsibilities For one of our sponsors we are looking for a Clinical Trial Manager to join the team here in Germany. This Local Study Manager is accountable for the strategic planning & management and performance of the assigned clinical trials from country allocation within feasibility process until study closure. This includes study timelines, study budget, and study conduct in accordance with the sponsors SOPs and ICH/GCP and regulatory guidelines & directives. This includes the ability to identify and anticipate risks jeopardizing the trial performance and to develop and initiate countermeasures based on proposer planning and regular revision of the plans. This position acts on country level as the key strategic interface with internal and external stakeholders to develop, implement, maintain, and improve operational processes to accelerate trial conduct in close collaboration with different functions and other departments, e.g. Medical Advisor, Site Engagement Manager, Strategic Start Up Manager, Medical Science Liaisons. This role acts as person of contact within a therapeutic area in terms of study management and conduct and leads a study team through change management efforts and by example. Qualifications: - Bachelor’s degree or higher degree in Health or Natural Sciences - Three years of experience in clinical research. - Experience in project management and certain time as field monitor or site coordinator. - International experienced preferred. - Fluency in German and English. - Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements - Excellent communication, presentation and interpersonal skills We are always excited to connect with great talent. This posting is intended for a [possible] upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.