12 Medical Oncology jobs in the United Kingdom

UK Vein Clinic – Join our team today!   

Job title: Vascular Doctor, private clinic shifts 

Location: Oxfordshire & London

About UK Vein Clinic  

UK Vein Clinic are a team of leading vascular surgeons and specialist practitioners that are dedicated to providing world-class clinical outcomes and patient experiences using minimally invasive varicose vein and thread vein treatment techniques. 

With varicose vein treatment increasingly restricted within the NHS, UK Vein Clinic was created to deliver accessible options to patients at a price that’s fair. Driven by the latest evidence and technology, and led by Professor Stephen Black, we’re really proud to be helping our patients get back to doing the things they love most. We are proud to offer a friendly, welcoming, and flexible environment for our staff.   

As a data-driven organisation, we’re doing our part to bring the future of health to more people with systems that work not just for our patients, but our clinical teams too. 

Job summary  

We’re excited to be looking for a new medical doctor to join our team to support the growing demand for varicose vein and thread vein treatment. 

We’re proud to be expanding our services across the UK and are looking for someone who is keen to work flexibly across Oxfordshire & London.

Although preferrable, those without specific experience in varicose and thread vein treatment will receive comprehensive training and hands-on learning opportunities to ensure you’re fully comfortable with the care pathway.  

Key responsibilities  

• Working in collaboration with our vascular scientists, you will be responsible for the diagnosis of varicose veins and thread veins in an initial diagnostic assessment appointment (consultation)  
• Sharing detailed information around the treatment of varicose veins or thread veins to the patient, and answering any questions they have 
• With training and where necessary, provide a clinical recommendation on the number of treatments required for effective thread vein removal 
• With training, deliver thread vein treatment for patients in clinic where varicose veins are not present 
• Conduct follow up appointments for patients following primary treatment, assessing how the patient is feeling, symptoms and conducting a brief ultrasound scan to confirm successful closure of treated varicose veins 
• Maintain excellent patient records during appointments using our patient app software 
• Work closely with colleagues to triage cases requiring further input (we have near immediate responses from senior clinical leadership) 
• Attend clinical specialty meetings to discuss the care pathway, training, or any support required   
• Provide a service for patients that is reassuring, compassionate and welcoming 

Required qualifications/screenings and skills  

• Medical Degree and valid license to practice in the United Kingdom 
• DBS check  
• Strong communication and interpersonal skills  
• Attention to detail and strong problem-solving abilities 
• Ability to work effectively in a team environment 

Preferred but not required skills  

• Experience in diagnosing and treating varicose veins  
• General practice experience is desirable but not essential 
• Knowledge of ultrasound imaging techniques  

This might be a good fit for you if  

• You’re a GP looking for a welcoming environment that prioritises strong team support – from the administrative team through to senior leadership 
• You’re exploring options to specialise and become an expert in vascular medicine 
• You’re willing to do a bit of travelling to nearby clinics to help support with increased patient demand 

Salary and benefits  

• Competitive salary 
• Clinical rotas reviewed and issued in advance 
• Flexible scheduling based on your availability 
• Discretionary bonus available 
• Discounts on treatments for you, family and friends  
• Team social events throughout the year 

The successful candidate will be reporting into our Lead Vascular GP.  

**Job Description Summary**
In this role, you will be leading the clinical development strategy of Molecular Imaging products under your responsibility in the Oncology and Immune-oncology domain. You will be responsible for designing and executing clinical development plans across the global businesses. As such, individual will have extensive cross-functional interaction within the Company, ranging from pre-clinical through to clinical, regulatory and commercial functions worldwide.
Our Pharmaceutical Diagnostics (PDx) business is the number one global supplier of contrast media and molecular imaging agents used to enhance medical imaging exams. Used throughout all major disease area diagnostic and treatment pathways, PDx products support three patients every second around the world.
Dans ce rôle, vous dirigerez la stratégie de développement clinique des produits d'imagerie moléculaire sous votre responsabilité dans le domaine de l'oncologie et de l'immuno-oncologie. Vous serez responsable de la conception et de l'exécution des plans de développement clinique à travers les activités mondiales. À ce titre, vous aurez de nombreuses interactions transversales au sein de l'entreprise, allant des fonctions précliniques aux fonctions cliniques, réglementaires et commerciales à l'échelle mondiale.
Notre activité de Diagnostic Pharmaceutique (PDx) est le principal fournisseur mondial d'agents de contraste et d'agents d'imagerie moléculaire utilisés pour améliorer les examens d'imagerie médicale. Utilisés dans toutes les principales voies de diagnostic et de traitement des maladies, les produits PDx soutiennent trois patients chaque seconde dans le monde.
**Job Description**
**Roles and Responsibilities**
+ To provide clinical leadership in cross-functional projects and product/project teams
+ To be responsible for the development and validation of the overall medical strategy of the assigned product(s) with appropriate internal or external experts, and for the agreement on this strategy with the appropriate internal business stakeholders
+ To be responsible that project activities are planned, agreed and executed according to the milestones and the overall clinical development plan (it includes pre- and post-marketing activities)
+ To be responsible for the timely and accurate completion of project documentation such as protocols, amendments, case report forms and study reports
+ To verify scientific accuracy of safety and efficacy summaries for regulatory/commercial purposes and to assist with the clinical sections of regulatory dossiers and or product specific scientific discussion, depending on pre or post-marketing activities
+ To work closely with the Risk Management, Compliance, Regulatory Affairs and Pharmacovigilance teams to establish and maintain strong risk assessment and management processes for decision making
+ To provide input into Risk Management reviews as it relates to patient safety, the performance of risk assessment in the design of clinical studies, and the interpretation of patient safety and risk in the post-market environment
+ To collaborate with multiple functions for identifying and selecting innovative products for development
+ To work with internal teams and external experts to design clinical development plan and to support clinical research strategies for regulatory approval, reimbursement and adoption.
**Rôles et Responsabilités**
+ Assurer le leadership clinique dans les projets et équipes produit/projet transversaux
+ Être responsable du développement et de la validation de la stratégie médicale globale des produits assignés en collaboration avec des experts internes ou externes, et s'assurer de l'accord sur cette stratégie avec les parties prenantes internes concernées
+ Veiller à ce que les activités du projet soient planifiées, convenues et exécutées selon les jalons et le plan global de développement clinique (y compris les activités pré- et post-commercialisation)
+ Être responsable de la réalisation en temps voulu et avec précision de la documentation du projet, tels que les protocoles, les amendements, les formulaires de rapport de cas et les rapports d'étude
+ Vérifier l'exactitude scientifique des résumés sur la sécurité et l'efficacité à des fins réglementaires ou commerciales, et aider à la rédaction des sections cliniques des dossiers réglementaires ou des discussions scientifiques spécifiques aux produits, en fonction des activités pré ou post-commercialisation
+ Travailler en étroite collaboration avec les équipes de gestion des risques, de conformité, des affaires réglementaires et de pharmacovigilance pour établir et maintenir des processus solides d'évaluation et de gestion des risques pour la prise de décision
+ Contribuer aux examens de gestion des risques en ce qui concerne la sécurité des patients, à l'évaluation des risques lors de la conception des études cliniques et à l'interprétation des risques et de la sécurité des patients dans l'environnement post-commercialisation
+ Collaborer avec plusieurs fonctions pour identifier et sélectionner des produits innovants à développer
+ Travailler avec les équipes internes et les experts externes pour concevoir un plan de développement clinique et soutenir les stratégies de recherche clinique pour l'approbation réglementaire, le remboursement et l'adoption.
**Required Qualifications**
+ Medical Degree
+ Substantial experience in Pharmaceutical, Biotech, or Contract Research Organization leading to good understanding of Clinical and Industry development of drug products.
+ A proven practice in Oncology and Immune oncology (preferably with Imaging diagnostic experience) in both academia and industry is requested.
+ Proven experience in Good Clinical Practice (GCP) Clinical trials
+ Must be willing to travel as required.
+ Experience working with Microsoft office products (Word, Excel, PowerPoint, Outlook)
**Qualifications Requises**
+ Diplôme de Médecin
+ Expérience significative dans l'industrie pharmaceutique, biotechnologique ou dans une organisation de recherche contractuelle, conduisant à une bonne compréhension du développement clinique et industriel des produits médicamenteux
+ Une expérience avérée en oncologie et immuno-oncologie (de préférence avec une expérience en diagnostic par imagerie) dans le milieu universitaire et industriel est demandée
+ Expérience confirmée des essais cliniques conformes aux Bonnes Pratiques Cliniques (BPC)
+ Disponibilité pour voyager selon les besoins
+ Expérience avec les produits Microsoft Office (Word, Excel, PowerPoint, Outlook)
**Desired Characteristics**
+ Excellent interpersonal, organization, communication, influencing skills.
+ Experience in managing KOLs, external experts. Brings his/her own network of KOLs, external experts.
+ Experience in scientific publications/communication
+ Experience managing complex projects and/or across global regions desirable.
+ Good team player with global mindset
+ Ability to work independently and with rigor
+ Good process knowledge, experience, and skills
+ Customer savvy.
**Caractéristiques Souhaitées**
+ Excellentes compétences interpersonnelles, d'organisation, de communication et d'influence
+ Expérience dans la gestion des leaders d'opinion clés (KOL), des experts externes. Possède son propre réseau de KOLs et d'experts externes
+ Expérience dans les publications/sciences de la communication
+ Expérience dans la gestion de projets complexes et/ou dans des régions mondiales souhaitée
+ Bon esprit d'équipe avec une mentalité mondiale
+ Capacité à travailler de manière indépendante et rigoureuse
+ Bonnes connaissances et compétences en matière de processus
+ Sens du client
**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.
**Inclusion et diversité**
GE HealthCare est un employeur offrant l'égalité des chances où l'inclusion compte. Les décisions relatives à l'emploi sont prises sans tenir compte de l'origine national ou ethnique, de la religion, du sexe, de l'orientation sexuelle, de l'identité ou de l'expression de genre, de l'âge, du handicap, du statut d'ancien combattant protégé ou d'autres caractéristiques protégées par la loi.
Nos rémunérations totales sont conçues pour libérer votre ambition en vous donnant la motivation et la flexibilité dont vous avez besoin pour transformer vos idées en réalités qui changent le monde. Nos salaires et nos avantages sociaux correspondent à tout ce que vous attendez d'une organisation ayant une dimension internationale, avec des possibilités de développement de carrière, dans une culture qui favorise la collaboration et le soutien.
**A propos de nous**
GE HealthCare est l'un des leaders mondiaux dans le domaine des technologies médicales et des solutions numériques. Il permet aux cliniciens de prendre des décisions plus rapides et plus pertinentes à travers des équipements intelligents, des analyses de données, des applications et des services. Avec plus de 100 ans d'expérience dans le secteur de la santé et environ 47 000 employés dans le monde, la société est au centre d'un écosystème qui travaille pour une médecine de précision.
#LI-MG1
#LI-hybrid
**Additional Information**
**Relocation Assistance Provided:** No

**Job Description Summary**
In this role, you will be leading the clinical development strategy of Molecular Imaging products under your responsibility in the Oncology and Immune-oncology domain. You will be responsible for designing and executing clinical development plans across the global businesses. As such, individual will have extensive cross-functional interaction within the Company, ranging from pre-clinical through to clinical, regulatory and commercial functions worldwide.
Our Pharmaceutical Diagnostics (PDx) business is the number one global supplier of contrast media and molecular imaging agents used to enhance medical imaging exams. Used throughout all major disease area diagnostic and treatment pathways, PDx products support three patients every second around the world.
Dans ce rôle, vous dirigerez la stratégie de développement clinique des produits d'imagerie moléculaire sous votre responsabilité dans le domaine de l'oncologie et de l'immuno-oncologie. Vous serez responsable de la conception et de l'exécution des plans de développement clinique à travers les activités mondiales. À ce titre, vous aurez de nombreuses interactions transversales au sein de l'entreprise, allant des fonctions précliniques aux fonctions cliniques, réglementaires et commerciales à l'échelle mondiale.
Notre activité de Diagnostic Pharmaceutique (PDx) est le principal fournisseur mondial d'agents de contraste et d'agents d'imagerie moléculaire utilisés pour améliorer les examens d'imagerie médicale. Utilisés dans toutes les principales voies de diagnostic et de traitement des maladies, les produits PDx soutiennent trois patients chaque seconde dans le monde.
**Job Description**
**Roles and Responsibilities**
+ To provide clinical leadership in cross-functional projects and product/project teams
+ To be responsible for the development and validation of the overall medical strategy of the assigned product(s) with appropriate internal or external experts, and for the agreement on this strategy with the appropriate internal business stakeholders
+ To be responsible that project activities are planned, agreed and executed according to the milestones and the overall clinical development plan (it includes pre- and post-marketing activities)
+ To be responsible for the timely and accurate completion of project documentation such as protocols, amendments, case report forms and study reports
+ To verify scientific accuracy of safety and efficacy summaries for regulatory/commercial purposes and to assist with the clinical sections of regulatory dossiers and or product specific scientific discussion, depending on pre or post-marketing activities
+ To work closely with the Risk Management, Compliance, Regulatory Affairs and Pharmacovigilance teams to establish and maintain strong risk assessment and management processes for decision making
+ To provide input into Risk Management reviews as it relates to patient safety, the performance of risk assessment in the design of clinical studies, and the interpretation of patient safety and risk in the post-market environment
+ To collaborate with multiple functions for identifying and selecting innovative products for development
+ To work with internal teams and external experts to design clinical development plan and to support clinical research strategies for regulatory approval, reimbursement and adoption.
**Rôles et Responsabilités**
+ Assurer le leadership clinique dans les projets et équipes produit/projet transversaux
+ Être responsable du développement et de la validation de la stratégie médicale globale des produits assignés en collaboration avec des experts internes ou externes, et s'assurer de l'accord sur cette stratégie avec les parties prenantes internes concernées
+ Veiller à ce que les activités du projet soient planifiées, convenues et exécutées selon les jalons et le plan global de développement clinique (y compris les activités pré- et post-commercialisation)
+ Être responsable de la réalisation en temps voulu et avec précision de la documentation du projet, tels que les protocoles, les amendements, les formulaires de rapport de cas et les rapports d'étude
+ Vérifier l'exactitude scientifique des résumés sur la sécurité et l'efficacité à des fins réglementaires ou commerciales, et aider à la rédaction des sections cliniques des dossiers réglementaires ou des discussions scientifiques spécifiques aux produits, en fonction des activités pré ou post-commercialisation
+ Travailler en étroite collaboration avec les équipes de gestion des risques, de conformité, des affaires réglementaires et de pharmacovigilance pour établir et maintenir des processus solides d'évaluation et de gestion des risques pour la prise de décision
+ Contribuer aux examens de gestion des risques en ce qui concerne la sécurité des patients, à l'évaluation des risques lors de la conception des études cliniques et à l'interprétation des risques et de la sécurité des patients dans l'environnement post-commercialisation
+ Collaborer avec plusieurs fonctions pour identifier et sélectionner des produits innovants à développer
+ Travailler avec les équipes internes et les experts externes pour concevoir un plan de développement clinique et soutenir les stratégies de recherche clinique pour l'approbation réglementaire, le remboursement et l'adoption.
**Required Qualifications**
+ Medical Degree
+ Substantial experience in Pharmaceutical, Biotech, or Contract Research Organization leading to good understanding of Clinical and Industry development of drug products.
+ A proven practice in Oncology and Immune oncology (preferably with Imaging diagnostic experience) in both academia and industry is requested.
+ Proven experience in Good Clinical Practice (GCP) Clinical trials
+ Must be willing to travel as required.
+ Experience working with Microsoft office products (Word, Excel, PowerPoint, Outlook)
**Qualifications Requises**
+ Diplôme de Médecin
+ Expérience significative dans l'industrie pharmaceutique, biotechnologique ou dans une organisation de recherche contractuelle, conduisant à une bonne compréhension du développement clinique et industriel des produits médicamenteux
+ Une expérience avérée en oncologie et immuno-oncologie (de préférence avec une expérience en diagnostic par imagerie) dans le milieu universitaire et industriel est demandée
+ Expérience confirmée des essais cliniques conformes aux Bonnes Pratiques Cliniques (BPC)
+ Disponibilité pour voyager selon les besoins
+ Expérience avec les produits Microsoft Office (Word, Excel, PowerPoint, Outlook)
**Desired Characteristics**
+ Excellent interpersonal, organization, communication, influencing skills.
+ Experience in managing KOLs, external experts. Brings his/her own network of KOLs, external experts.
+ Experience in scientific publications/communication
+ Experience managing complex projects and/or across global regions desirable.
+ Good team player with global mindset
+ Ability to work independently and with rigor
+ Good process knowledge, experience, and skills
+ Customer savvy.
**Caractéristiques Souhaitées**
+ Excellentes compétences interpersonnelles, d'organisation, de communication et d'influence
+ Expérience dans la gestion des leaders d'opinion clés (KOL), des experts externes. Possède son propre réseau de KOLs et d'experts externes
+ Expérience dans les publications/sciences de la communication
+ Expérience dans la gestion de projets complexes et/ou dans des régions mondiales souhaitée
+ Bon esprit d'équipe avec une mentalité mondiale
+ Capacité à travailler de manière indépendante et rigoureuse
+ Bonnes connaissances et compétences en matière de processus
+ Sens du client
**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.
**Inclusion et diversité**
GE HealthCare est un employeur offrant l'égalité des chances où l'inclusion compte. Les décisions relatives à l'emploi sont prises sans tenir compte de l'origine national ou ethnique, de la religion, du sexe, de l'orientation sexuelle, de l'identité ou de l'expression de genre, de l'âge, du handicap, du statut d'ancien combattant protégé ou d'autres caractéristiques protégées par la loi.
Nos rémunérations totales sont conçues pour libérer votre ambition en vous donnant la motivation et la flexibilité dont vous avez besoin pour transformer vos idées en réalités qui changent le monde. Nos salaires et nos avantages sociaux correspondent à tout ce que vous attendez d'une organisation ayant une dimension internationale, avec des possibilités de développement de carrière, dans une culture qui favorise la collaboration et le soutien.
**A propos de nous**
GE HealthCare est l'un des leaders mondiaux dans le domaine des technologies médicales et des solutions numériques. Il permet aux cliniciens de prendre des décisions plus rapides et plus pertinentes à travers des équipements intelligents, des analyses de données, des applications et des services. Avec plus de 100 ans d'expérience dans le secteur de la santé et environ 47 000 employés dans le monde, la société est au centre d'un écosystème qui travaille pour une médecine de précision.
#LI-MG1
#LI-hybrid
**Additional Information**
**Relocation Assistance Provided:** No

**Job Overview**
The medical department consists of a Chief Medical Officer, Medical Directors, Sr Medical Directors, Medical Writers, and Safety Associates. The Medical Director provides medical and scientific support to clinical research programs, study teams and investigators. The Medical Director also provides review, advice, and leadership for potentially or awarded clinical research programs.
The Medical Director role is a team member participant role and functions in a matrix report to project teams much like other members of the project teams. The primary role of Medical Director is to provide medical oversight for clinical trials by serving as Medical Monitor for studies conducted by IQVIA Biotech Clinical on behalf of sponsor companies. The principal function of a Medical Monitor is to serve as primary contact for the sponsor medical team and to serve as front line medical resource to support the project team. The Medical Monitor is customarily available 24/7 to answer questions from site coordinators and investigators on protocol inclusion/exclusion criteria, protocol clarifications, and compliance issues, and to provide review of alert labs per sponsor preference. Major duties of the Medical Director are outlined below:
**Essential Functions**
Functions as project team member:
+ Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, informed consent, Investigator Drug Brochures, eCRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation, and reporting.
+ Ensures medical activities run according to GCP and operate with highest efficiency.
+ Establishes and maintains a network of medical/scientific consultants, etc.
+ Supervises and manages Medical Director activities.
Clinical Activities:
+ Interacts with clients regarding drug development programs, study design and protocol.
+ Reviews and provides input for protocol development. Interacts with key thought leaders and/or sponsor representatives to develop inclusion/exclusion criteria and study endpoints.
+ Interacts in team approach to develop statistical and data management sections of the protocol.
+ Reviews the final protocol for clinical, safety and efficacy variables.
+ Provides project team training on protocol and/or therapeutic areas.
+ Assists team with developing criteria for investigator site selection and networking for potential investigators for study participation. Aids in review and final selection.
+ Participates in subject recruitment and retention activities including individual calls to key opinion leaders, investigators, and site staff and/or participation in teleconference and WebEx presentations.
+ Presents protocol and/or safety reporting information at investigator meetings.
+ Develops project medical monitoring plans as requested.
+ Provides on call coverage for protocol queries and site support.
+ Provides first line contact for investigators and monitors regarding study related medical/safety issues and resolution of study protocol and patient eligibility issues.
Safety Monitoring and SAE Reporting Activities:
+ Verifies the medical accuracy of patient safety data and maintains an ongoing assessment of the safety profile of the study.
+ Provides medical review of SAE reporting, writes and/or reviews SAE narratives, and works with the Safety Management Department to track SAEs and follow-up on outstanding safety queries, interacts with sponsor and discusses safety issues with site as needed.
+ Reviews IND/SUSAR Safety Reports (per sponsor preference), updates to Investigator Brochures, and annual IND reports with sponsor data.
+ In consultation with the sponsor, follow procedures for acquiring knowledge of subject treatment assignments (i.e. breaking the blind).
+ Interact with appropriate FDA officials concerning safety and other study related issues, as requested.
Data Activities:
+ Provides medical review of eCRFs for clinical accuracy.
+ Provides medical review of data analysis plan.
+ Reviews safety fields at case freeze for reconciliation (if needed).
+ Works with data group to reconcile SAE events as needed.
+ Reviews medical coding of adverse events, laboratory data and concomitant medications for accuracy, coherence, consistency, and trends.
+ Reviews data tables, listings, and figures.
+ Reviews and/or writes portions of final clinical study report.
DSMB/Adjudication Committee Activities:
+ May assist sponsor in choosing committee members.
+ May serve as a non-voting member to convene and organize proceedings.
+ May develop operating guidelines in conjunction with committee members and submits these to sponsor for review.
+ May determine data flow with sponsor to ensure reporting accuracy.
+ Can ensure DSMB feedback is given to sites for IRBs.
+ All DSMB activities are usually managed by the IQVIA Biotech Oversight Management Group and not the IQVIA Biotech medical monitor.
Business Development Activities:
+ Work with Business Development to actively solicit new business for Novella Clinical, including assistance with marketing presentations and proposal development.
+ Supports business development activities with proposal development and sales presentations.
+ Participates in feasibility discussions relating to specific project proposals.
Special Projects:
+ Obtain literature searches to acquire background information for study proposals, preparation of training sessions, and interpretation of clinical data, report writing, etc.
+ Assists with drafting of standard operating procedures and working practices regarding all Medical Director activities.
+ Participate in a variety of team quality improvement efforts as necessary.
+ Perform other related duties as assigned or requested by the Chief Medical Officer.
**Qualifications**
+ Medical Degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.
+ 10 years of experience is required which can include medical practice (hospital/clinic), academia, clinical research, or drug development.
+ 3-5 years of biopharmaceutical (industry) experience is preferred which can be part of the 10-year experience.
+ Ability to work in partnership with a multidisciplinary group of colleagues, including translating concepts into practical approaches and promoting consensus.
+ Outstanding ability to work independently with minimal supervision, ability to work effectively within a team, and matrix environment.
+ Ability to organize and work efficiently on several projects, each with specific requirements and/or shifting priorities.
+ Excellent oral and written communications skills as well as interpersonal skills are essential.
**Oncology / Hematology**
+ Current or prior license to practice medicine; board certification/eligibility ideal (Preference)
+ Board Certified / Board Eligible: Oncology/ Hematology (Required)
**Applicants must have experience in at least one of the following areas: Hematology (Non-Malignant) , Hematological Malignancies ,Solid Tumor Oncology , Radiation Oncology / Radiation Therapy , Pediatric Hematology / Oncology , Histopathology / Pathology , Gynecology or Urology.**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

IQVIA is seeking a scientifically credible and field-based Medical Science Liaison (MSL) to support a pivotal oncology clinical trial across the UK, Ireland, and Belgium. You'll be a key scientific partner to clinical trial sites-engaging with investigators, supporting site activation and enrollment, and facilitating high-quality scientific exchange.
**Key Responsibilities:**
+ Provide field-based medical support to clinical research programs in oncology.
+ Deliver credible, balanced presentations on disease area and investigational therapies to investigators and site staff.
+ Engage with clinical trial sites to understand and help resolve medical barriers to patient recruitment and screening.
+ Collaborate with site management and monitoring teams to support site initiation and engagement.
+ Facilitate compliant scientific exchange with healthcare professionals (HCPs) and key opinion leaders (KOLs).
+ Capture and report field intelligence, including protocol feedback, treatment landscape insights, and competitor activity.
+ Represent the program at scientific meetings, advisory boards, and congresses.
+ Maintain up-to-date knowledge of the disease area, investigational assets, and relevant clinical data.
+ Ensure all activities are conducted in accordance with applicable laws, regulations, and company policies.
**Required Qualifications:**
+ Advanced scientific degree: MD, PhD, PharmD (strongly preferred); master's degree may be considered with relevant experience.
+ Minimum 2 years' experience as an MSL or in a scientific/medical role.
+ Oncology experience is essential, ideally in solid tumors (head & neck, thoracic, or gastrointestinal).
+ Strong understanding of clinical trial operations and site engagement strategies.
+ Fluent in English and ideally one additional language relevant to the territory (e.g., French or Dutch).
+ Right to work in the UK as well as willingness to travel across the UK, Ireland, and Belgium.
+ Valid driver's license.
**Why This Role Matters:**
+ Represent a first-in-class therapeutic approach with a dual mechanism of action.
+ Join a global MSL team deployed across 26 countries.
+ Influence trial success through strategic site engagement and real-time insights.
+ Grow your career in a fast-paced, science-led environment where your expertise matters.
Ready to make a difference in oncology? Apply now and bring your scientific expertise, curiosity, and collaborative spirit to a program that puts patients first and science at the center.
#LI-CES
#LI-CS1
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
**Job Description**
The Medical Director of Hematology/Oncology provides medical monitoring to multiple clinical trials. Additionally, the Medical Director guides the project teams to design and implement clinical studies at high quality and in a time and cost-effective manner in line with the department and corporate goals and within regulatory and resource guidelines.
**Responsibilities**
+ Provide medical monitoring to multiple hematology/oncology clinical trials
+ Lead project/study teams to design and implement hematology/oncology clinical studies
+ Write protocols, investigator brochures, clinical study reports and review clinical trial documents
+ Conduct investigator meetings and lead site initiation visits with clinical trial investigators
+ Implement and deploy drug development strategic plans, develop contingency plans, provide technical and strategic advice, and meet milestones and budgets
+ Translate findings from research and nonclinical studies into clinical development opportunities
+ Interact with clinical investigators and thought leaders
+ Work with internal regulatory affairs team and other ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with these external guidelines
+ Work with internal pre-clinical scientists, translational scientists, business and commercial organizations in a cross functional manner.
+ Work in a cross-functional team environment, including with clinical operations, biomarker specialists, CROs, and regulatory affairs
+ Provide clinical expertise and input for regulatory filings (i.e., BLA, MAA) as well as response to questions from regulatory authorities in the context of IND submissions, clinical trial applications or filing procedures
+ Provide clinical guidance and work in a team environment in interactions with external stakeholders (medical experts, advisory boards, patient advocacy groups) and internal stakeholders (Research, Translational Sciences, Clinical Operations, Safety, Regulatory, Medical Affairs, and Commercial)
**Requirements:**
+ MD/DO degree and clinical development experience in the pharmaceutical industry.
+ Board certification/specialization in Hematology or Oncology and experience managing oncology trials.
+ CAR-T therapeutic area experience (preferred)
+ Multiple myeloma disease area expertise (required)
+ Phase 2 or 3 study experience within the pharmaceutical industry.
+ Relevant drug development experience, either within industry or as a clinical investigator/physician scientist in academia, or equivalent experience.
+ Demonstrated clinical development strategist with experience designing, implementing, and conducting clinical trials, with emphasis on late-stage clinical development.
+ Knowledge of carrying out hematology/oncology clinical trials, including knowledge of hematology/oncology treatment options
+ Strategic leadership and tactical skills, excellent initiative, and judgment
+ Demonstrated ability to develop and maintain excellent working relationships with both internal colleagues and external contacts, including key thought leaders, and investigators
+ Demonstrated ability to work well in teams in a cross functional manner
+ Ability to communicate and work in a self-guided manner with scientific/technical personnel
+ Ability to think critically, and demonstrated troubleshooting and problem-solving skills
+ Self-motivated and willing to accept temporary responsibilities outside of initial job description
+ Comfortable in a dynamic small company environment with minimal direction and able to adjust workload based upon changing priorities
+ May travel up to 25%
+ Must be based in Stockley Park Gilead Office
**Equal Employment Opportunity (EEO)**
It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual's gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.
**For Current Gilead Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.