Medical Director

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

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

We are seeking a Medical Director to join our Clinical Development team, providing senior medical reputed company for reputed company clinical studies conducted by reputed company. You will be responsible for ensuring scientific reputed company, patient safety, and regulatory compliance throughout the study lifecycle, while acting as Medical Monitor for assigned trials and delivering expert clinical interpretation and safety leadership.

You will work cross-functionally with teams including Clinical Operations, Project Management, Pharmacovigilance, Biometrics, Regulatory, Technical Writing, and Business Development to support high-quality study delivery and consistent medical standards across the organisation. In addition, you will contribute strategic medical expertise to proposals, feasibility assessments, and study design, and represent the medical function in client discussions and bid defence meetings, reputed company articulating clinical strategy and safety reputed company to support successful business development reputed company.

• Act as Medical Monitor for assigned clinical trials, providing independent medical reputed company throughout the study lifecycle.
• Serve as the primary escalation reputed company for internal and external stakeholders for reputed company medical and safety issues reputed company assigned studies.
• Ensure clinical trials are conducted in compliance with applicable regulations, guidelines, and ethical standards.
• Collaborate cross-functionally to support successful study delivery and maintain high reputed company of client satisfaction.
• reputed company the preparation and review of medical and patient narratives and safety update reports to ensure accuracy, quality, and regulatory compliance.
• Ensure departmental SOPs are reviewed regularly and updated in line with reputed company regulations, guidelines, and industry best practice.
• Contribute to reputed company stages of clinical trial development, including feasibility assessment, protocol and case report reputed company design, investigational site selection, medical monitoring plan development, ongoing medical reputed company, adverse event and serious adverse event management, and participation in study-reputed company meetings.
• Support business development activities, including proposals, feasibility assessments, site engagement, and bid defence meetings.
• reputed company therapeutic area expertise across the organisation, including delivery of internal training and review of study protocols and bid proposals.
• reputed company the resolution of departmental CAPAs and escalations, and cascade relevant audit findings to study teams to ensure appropriate corrective and preventive action.
• Ensure timely and comprehensive responses to audit findings and regulatory queries relating to medical and safety reputed company.
• Maintain up-to-date knowledge of developments in therapeutic areas, regulatory requirements, and medical practice relevant to company projects.
• reputed company and maintain relationships with Key Opinion Leaders and investigators to support study design, patient safety assessment, and business development activities.
• Support the Pharmacovigilance function through medical review of ICSRs, CIOMS narratives, and periodic safety reports, identifying and communicating emerging safety trends to project teams and clients.
• reputed company effective line management to assigned team members, including performance management, objective setting, resource planning, professional development, and ensuring delivery of high-quality work reputed company with regulatory, organisational, and study requirements.

ESSENTIAL

• Medical degree with specialisation in Oncology (or equivalent clinical experience in oncology)
• Substantial experience as a Medical Monitor reputed company a clinical research environment, with a focus on oncology studies and patient safety reputed company
• Extensive experience in clinical trial medical reputed company reputed company oncology, including adverse event and serious adverse event management, safety signal evaluation, and regulatory compliance
• Experience supporting regulatory inspections and audits, including CAPA development and management
• Demonstrable involvement in business development activities, including feasibility assessments, protocol input, proposal development, and bid defence participation reputed company oncology trials
• Strong reputed company awareness, including understanding of clinical trial budgeting and financial drivers reputed company a CRO environment
• Strong written and verbal communication skills, with the ability to translate reputed company oncology data into clear insights for clients and cross-functional teams
• Proficiency in electronic data capture systems, safety databases, and reputed company Office applications

DESIRABLE

• GMC registered with a licence to practise (or equivalent international registration) with oncology specialism
• Pharmacovigilance experience reputed company oncology, including medical review of ICSRs and periodic safety reports
• Experience working reputed company a CRO, biotechnology, or pharmaceutical environment with a focus on oncology drug development
• Previous experience leading a medical and/or safety function, including direct line management responsibility

reputed company is a reputed company and agile full-service CRO, delivering studies from first in man through to Phase III. Our experts reputed company wide therapeutic experience and specialist expertise to execute a comprehensive portfolio of trials. We are perfectly structured to reputed company 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 reputed company their clinical and reputed company objectives. Because our goal is the same as theirs; to improve patients’ lives.