• Deliver competent, high-quality nursing care to study patients in their homes. • Accountable for the competent and confident delivery of high-quality clinical care to patients/participants. Ensure compliance with each study’s protocol by providing thorough review and documentation at each subject study visit. • Administer investigational medications/products as needed; Perform patient assessments to determine presence of side effects; notify Principal Investigator of findings/issues. • Perform medical tests as outlined in protocol, including, but not limited to: vital signs, specimen collection, electrocardiograms; Process specimens and ship specimens per protocol. • Provide patient education and medical information to study patients to ensure understanding of proper medication dosage, administration, and disease treatment. • Responsible for adherence to clinical research policies to ensure ethical conduct and protect vulnerable populations. • Communicate effectively, promoting open and trusting relationships.

Manage clinical trials by coordinating patient enrollment and follow-up, maintaining regulatory and data documentation, assisting with study start-up, and collaborating with clinical teams to ensure accurate and timely data collection.

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.