33 Oncology jobs in the United Kingdom
Clinical Oncology Consultant
Posted 86 days ago
Job Viewed
Job Description
Contact
Experience Required: NHS experience essential
We are seeking an experienced and dedicated Clinical Oncology Consultant to join a leading healthcare provider in Derby . This permanent role offers an excellent opportunity to contribute to a dynamic oncology team, providing high-quality cancer care within an NHS setting.
Key Responsibilities:- Provide specialist clinical oncology services, including chemotherapy and radiotherapy treatment planning.
- Lead and support multidisciplinary team meetings, collaborating with oncologists, radiologists, surgeons, and other healthcare professionals.
- Develop and implement patient treatment plans, ensuring the highest standards of care and patient safety.
- Supervise and train junior doctors, nurses, and other healthcare staff.
- Participate in research, audits, and quality improvement initiatives within the department.
- Maintain up-to-date knowledge of advancements in oncology treatments and best practices.
- Engage in teaching activities for medical students and junior staff.
- Contribute to service development and clinical governance within the department.
Requirements
Full GMC registration with a license to practice.
CCT (Certificate of Completion of Training) in Clinical Oncology or eligibility within six months.
Extensive NHS experience in oncology.
Strong leadership, communication, and team-working skills.
Experience in chemotherapy, radiotherapy planning, and multidisciplinary team collaboration.
Benefits
- Competitive salary and NHS benefits package.
- Opportunities for professional development and research.
- Supportive and well-established oncology department.
- Access to state-of-the-art treatment facilities and cutting-edge technology.
If you are an experienced Clinical Oncology Consultant looking for a new opportunity in Derby , we would love to hear from you.
Medical Director, Clinical Development - Hematology/Oncology
Posted 13 days ago
Job Viewed
Job Description
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.
Bank Oncology / Chemotherapy Nurse
Posted 2 days ago
Job Viewed
Job Description
Bank Oncology Nurse | Oadby, Leicester | Competitive rates, plus enhancements | Bank contract | No nights | Monday - Friday, 8am-6pm |
Due to our oncology service increasing, Spire Leicester Hospital are looking for experienced oncology nurses to join our team of bank nurses on our 17 bedded, purpose-built, dedicated oncology and haematology unit.
Working alongside a team of 12 Nurses, 1 HCA and several consultants, you will receive a huge level of support from your team members.
We promote a good work/life balance and to support this you will work no nights or weekends and very rare bank holidays.
Founded in 1989, Spire Leicester is a high performing hospital with a great track record in superior patient care. We practice some of the most advanced treatments on the latest generation imaging, and diagnostic technology, meaning we can offer everything from screening, rehabilitation and cutting-edge surgical procedures in specialist fields like orthopaedics and cancer care.
Duties and responsibilities :
To provide safe administration of Systemic Anti-Cancer Therapy, specialist nursing care of central lines, assist in oncology clinics, provide advice and support to oncology and haematology patients and their family members. The service provided will primarily be for the daycare oncology unit and outpatients but you may also be required to support the care of patients admitted to the ward from the unit.
What are we looking for?
- Current oncology experience li>NMC Registered Nurse, with no restrictions
- A positive attitude and team player
- Strong communication skills
- Cannulation and venepuncture trained
- You must be SACT administration trained
Benefits
We offer employees a competitive salary as well as a comprehensive benefits package which includes but is not limited to:
- 35 days annual leave inclusive of bank holidays
- Employer and employee contributory pension with flexible retirement options
- 'Spire for you' reward platform - discount and cashback for over 1000 retailers
- Free Bupa wellness screening
- Private medical insurance
- Life assurance
- Free onsite parking
Please see the attached benefits leaflet for more information.
We commit to our employees well-being through work life balance, on-going development, support and reward.
Spire Healthcare is a leading independent hospital group in the United Kingdom and the largest in terms of revenue. From 39 hospitals and 8 clinics across England, Wales and Scotland, Spire Healthcare provides diagnostics, inpatient, day case and outpatient care.
For further information about this role or for an informal conversation about the range of career options available with Spire please contact Hananh Radford on (url removed)
For us, it's more than just treating patients; it's about looking after people .
Closing date: In order to streamline our recruitment process, we reserve the right to expire vacancies prior to the advertised closing date once we have received a sufficient number of applications
Bank Oncology / Chemotherapy Nurse
Posted 2 days ago
Job Viewed
Job Description
Bank Oncology Nurse | Oadby, Leicester | Competitive rates, plus enhancements | Bank contract | No nights | Monday - Friday, 8am-6pm |
Due to our oncology service increasing, Spire Leicester Hospital are looking for experienced oncology nurses to join our team of bank nurses on our 17 bedded, purpose-built, dedicated oncology and haematology unit.
Working alongside a team of 12 Nurses, 1 HCA and several consultants, you will receive a huge level of support from your team members.
We promote a good work/life balance and to support this you will work no nights or weekends and very rare bank holidays.
Founded in 1989, Spire Leicester is a high performing hospital with a great track record in superior patient care. We practice some of the most advanced treatments on the latest generation imaging, and diagnostic technology, meaning we can offer everything from screening, rehabilitation and cutting-edge surgical procedures in specialist fields like orthopaedics and cancer care.
Duties and responsibilities :
To provide safe administration of Systemic Anti-Cancer Therapy, specialist nursing care of central lines, assist in oncology clinics, provide advice and support to oncology and haematology patients and their family members. The service provided will primarily be for the daycare oncology unit and outpatients but you may also be required to support the care of patients admitted to the ward from the unit.
What are we looking for?
- Current oncology experience li>NMC Registered Nurse, with no restrictions
- A positive attitude and team player
- Strong communication skills
- Cannulation and venepuncture trained
- You must be SACT administration trained
Benefits
We offer employees a competitive salary as well as a comprehensive benefits package which includes but is not limited to:
- 35 days annual leave inclusive of bank holidays
- Employer and employee contributory pension with flexible retirement options
- 'Spire for you' reward platform - discount and cashback for over 1000 retailers
- Free Bupa wellness screening
- Private medical insurance
- Life assurance
- Free onsite parking
Please see the attached benefits leaflet for more information.
We commit to our employees well-being through work life balance, on-going development, support and reward.
Spire Healthcare is a leading independent hospital group in the United Kingdom and the largest in terms of revenue. From 39 hospitals and 8 clinics across England, Wales and Scotland, Spire Healthcare provides diagnostics, inpatient, day case and outpatient care.
For further information about this role or for an informal conversation about the range of career options available with Spire please contact Hananh Radford on (url removed)
For us, it's more than just treating patients; it's about looking after people .
Closing date: In order to streamline our recruitment process, we reserve the right to expire vacancies prior to the advertised closing date once we have received a sufficient number of applications
Medical Engagement Strategy - Haematology & Oncology
Posted 4 days ago
Job Viewed
Job Description
Our client, a global pharmaceutical company, is currently looking for a Associate Director Medical Engagement Strategy to join their team in Uxbridge on a full time, 12-month temporary basis (35 hours per week - hybrid working).
You will pay a key role in ensuring the medical strategies within the oncology and haematology therapy area are being translated into the field teams successfully.
Key Responsibilities
- Overseeing the operational development and implementation of successful strategies and programs for the oncology and haematology therapy areas
- Supporting the team in sharing and implementing best practices across the haematology/oncology market
- Acting as project manager for live and virtual events as required as well as providing operational support on global team meetings
- Collaborating with stakeholders over market analytics to ensure it is aligned with objectives
- Liaising with other teams across the business over budget management
Requirements
- Previous Scientific background in a field management position such as MSL/Sales in the pharmaceutical or biotechnology industry
- Experience in developing Medical strategies for a therapy area
- Strong experience and knowledge around the oncology/haematology therapy area
- Ability to lead and influence in a matrix organisation
- Good understanding of regulatory policies within the industry
- Excellent communication and interpersonal skills
- Ability to travel across the country and internationally
Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Business in relation to this role.
Medical Engagement Strategy - Haematology & Oncology
Posted 6 days ago
Job Viewed
Job Description
Our client, a global pharmaceutical company, is currently looking for a Associate Director Medical Engagement Strategy to join their team in Uxbridge on a full time, 12-month temporary basis (35 hours per week - hybrid working).
You will pay a key role in ensuring the medical strategies within the oncology and haematology therapy area are being translated into the field teams successfully.
Key Responsibilities
- Overseeing the operational development and implementation of successful strategies and programs for the oncology and haematology therapy areas
- Supporting the team in sharing and implementing best practices across the haematology/oncology market
- Acting as project manager for live and virtual events as required as well as providing operational support on global team meetings
- Collaborating with stakeholders over market analytics to ensure it is aligned with objectives
- Liaising with other teams across the business over budget management
Requirements
- Previous Scientific background in a field management position such as MSL/Sales in the pharmaceutical or biotechnology industry
- Experience in developing Medical strategies for a therapy area
- Strong experience and knowledge around the oncology/haematology therapy area
- Ability to lead and influence in a matrix organisation
- Good understanding of regulatory policies within the industry
- Excellent communication and interpersonal skills
- Ability to travel across the country and internationally
Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Business in relation to this role.
Senior Local Trial Manager,Oncology
Posted 13 days ago
Job Viewed
Job Description
**Job Function:**
R&D Operations
**Job Sub** **Function:**
Clinical Trial Project Management
**Job Category:**
Professional
**All Job Posting Locations:**
High Wycombe, Buckinghamshire, United Kingdom
**Job Description:**
**Senior Local Trial Manager, Oncology**
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at
We are searching for the best talent for **2 x Senior Local Trial Managers** (Senior LTMs) who will be responsible for the local/UK management and oversight of clinical trials (or Medical Affairs data generation activity).
The head office location is in **High Wycombe** , Buckinghamshire (moving to Maidenhead mid-2026), and this position is **hybrid** (requiring 3 days per week on-site). Preferably the candidate will have experience working in Oncology.
The Senior LTM is the primary point of contact at a country level for assigned studies and has operational oversight of assigned protocols from start-up through to database lock and closeout activities. The Senior LTM is responsible for proactively coordinating and leading the local trial team to deliver quality data and trial documents/records that are compliant with the assigned clinical trial protocol, company Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and regulatory standards. The Senior LTM will actively contribute to process improvement, training and mentoring of Clinical Trial Assistant (CTA) and Site Manager (SM) roles. The Senior LTM may have some site management responsibilities.
You need a flexible mindset and have the ability to work in a constantly evolving environment. You will be part of a hardworking, enthusiastic, and committed team eager to deliver and helping to improve the lives of millions of patients.
_Are you ready to join our team? Then please read further!_
**You will be responsible for:**
Collaborating with the Manager, Clinical Operations (MCO) for country protocol and site feasibility assessments. Ensuring consistent and high quality conduct of site qualification visits and country feasibility reports. Recommending suitable sites for selection. Setting predictable and realistic start up timelines.
Leading and coordinating trial activities in compliance with SOPs, other procedural documents and regulations. Leading local project planning activities to meet recruitment targets and to deliver high quality data on time and within budget.
Acting as the subject matter expert for assigned protocols. Developing strong therapeutic knowledge.
Acting as primary country contact for a trial. Establishing and maintaining excellent working relationships with external organisations, in particular investigators, study trial coordinators and other site staff; and internal partners, including Medical Affairs.
Maintaining and updating trial management systems. Using study tools and management reports available to analyse trial progress.
Monitoring country progress and initiating Corrective and Preventive Actions when the trial deviates from plan. Identifying and resolving issues. Communicating study progress and issues to local and global study management teams.
Reviewing and approving Monitoring Visit Reports submitted by Site Managers; identifying issues and/or trends across a trial project.
Preparing IRAS submissions and responsibility for approvals during the trial.
**Qualifications / Requirements:**
BA or BSc degree in Life Sciences, Nursing or related scientific field (or equivalent experience) is required.
A minimum of 3 years of UK clinical trial experience is preferred. Experience of managing Oncology studies would be an advantage!
Should have proven understanding of the drug development process including GCP and local regulatory requirements.
Proficient in speaking and writing the English language.
Excellent written and oral communication skills.
Strong leadership skills; demonstrated ability to lead initiatives/small teams.
Ability to work on multiple trials in parallel, if required.
Flexibility to commute 3 days per week to High Wycombe office.
**Benefits:**
We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority, we have a flexible working environment as we value work-life balance. We offer career development opportunities for those who want to grow and be part of our organisation.
Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will be considered for employment without regard to any other characteristic protected by law. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
**#LI-Hybrid**
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Senior Local Trial Manager,Oncology
Posted 13 days ago
Job Viewed
Job Description
**Job Function:**
R&D Operations
**Job Sub** **Function:**
Clinical Trial Project Management
**Job Category:**
Professional
**All Job Posting Locations:**
High Wycombe, Buckinghamshire, United Kingdom
**Job Description:**
**Senior Local Trial Manager, Oncology**
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at
We are searching for the best talent for **2 x Senior Local Trial Managers** (Senior LTMs) who will be responsible for the local/UK management and oversight of clinical trials (or Medical Affairs data generation activity).
The head office location is in **High Wycombe** , Buckinghamshire (moving to Maidenhead mid-2026), and this position is **hybrid** (requiring 3 days per week on-site). Preferably the candidate will have experience working in Oncology.
The Senior LTM is the primary point of contact at a country level for assigned studies and has operational oversight of assigned protocols from start-up through to database lock and closeout activities. The Senior LTM is responsible for proactively coordinating and leading the local trial team to deliver quality data and trial documents/records that are compliant with the assigned clinical trial protocol, company Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and regulatory standards. The Senior LTM will actively contribute to process improvement, training and mentoring of Clinical Trial Assistant (CTA) and Site Manager (SM) roles. The Senior LTM may have some site management responsibilities.
You need a flexible mindset and have the ability to work in a constantly evolving environment. You will be part of a hardworking, enthusiastic, and committed team eager to deliver and helping to improve the lives of millions of patients.
_Are you ready to join our team? Then please read further!_
**You will be responsible for:**
Collaborating with the Manager, Clinical Operations (MCO) for country protocol and site feasibility assessments. Ensuring consistent and high quality conduct of site qualification visits and country feasibility reports. Recommending suitable sites for selection. Setting predictable and realistic start up timelines.
Leading and coordinating trial activities in compliance with SOPs, other procedural documents and regulations. Leading local project planning activities to meet recruitment targets and to deliver high quality data on time and within budget.
Acting as the subject matter expert for assigned protocols. Developing strong therapeutic knowledge.
Acting as primary country contact for a trial. Establishing and maintaining excellent working relationships with external organisations, in particular investigators, study trial coordinators and other site staff; and internal partners, including Medical Affairs.
Maintaining and updating trial management systems. Using study tools and management reports available to analyse trial progress.
Monitoring country progress and initiating Corrective and Preventive Actions when the trial deviates from plan. Identifying and resolving issues. Communicating study progress and issues to local and global study management teams.
Reviewing and approving Monitoring Visit Reports submitted by Site Managers; identifying issues and/or trends across a trial project.
Preparing IRAS submissions and responsibility for approvals during the trial.
**Qualifications / Requirements:**
BA or BSc degree in Life Sciences, Nursing or related scientific field (or equivalent experience) is required.
A minimum of 3 years of UK clinical trial experience is preferred. Experience of managing Oncology studies would be an advantage!
Should have proven understanding of the drug development process including GCP and local regulatory requirements.
Proficient in speaking and writing the English language.
Excellent written and oral communication skills.
Strong leadership skills; demonstrated ability to lead initiatives/small teams.
Ability to work on multiple trials in parallel, if required.
Flexibility to commute 3 days per week to High Wycombe office.
**Benefits:**
We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority, we have a flexible working environment as we value work-life balance. We offer career development opportunities for those who want to grow and be part of our organisation.
Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will be considered for employment without regard to any other characteristic protected by law. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
**#LI-Hybrid**
Territory Manager - Interventional Oncology (North)
Posted 6 days ago
Job Viewed
Job Description
We are looking for an experienced and customer-focused Territory Sales Manager to join our BD Interventional business unit. In this field-based sales role, you will be responsible for driving the commercial success of our PleurX product portfolio, including solutions for ascites and pleural drainage, by understanding clinical needs and providing tailored solutions to healthcare professionals. Reporting to the National Sales Manager, you will play a key role in supporting existing accounts and identifying new opportunities across your territory. This is a field role with regular travel across the North UK and occasional international meetings. Your preferred location is around Leeds.
**Job Description**
**We are the makers of possible**
BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
**Why join us?**
BD is proud to be certified as a Top Employer 2025 in United Kingdom, reflecting our commitment to creating an exceptional working environment.
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.
Become a **maker of possible** with us!
**Main responsibilities will include:**
+ Achieve and exceed quarterly and annual sales targets in line with business plans
+ Develop and maintain strong, trust-based relationships with healthcare professionals and clinical teams
+ Deliver excellent customer service and support throughout the sales cycle
+ Identify new commercial opportunities, particularly within strategic accounts
+ Provide market insights and competitor intelligence to support strategic planning
+ Maintain accurate and up-to-date customer data in the CRM system
+ Collaborate cross-functionally to support national sales initiatives and team objectives
+ Ensure full compliance with all relevant policies, procedures, and regulatory requirements
**About you:**
+ Minimum of 2 years' experience in medical device sales, preferably within respiratory, oncology, or gastroenterology
+ Proven track record of achieving commercial targets
+ Excellent communication, influencing, and negotiation skills
+ Highly organised with strong time management abilities
+ Confident using digital tools and CRM systems
+ Full UK driving licence and willingness to travel frequently
**Target s** **alary range for the role:** **£4** **5.000** **to** **£5.000** **+ bonus + benefits**
**Click on apply if this sounds like you!**
Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.
**To learn more about BD visit:** ** Skills
Business Planning, Computer Literacy, Driving Sales, Interpersonal Communication, Medical Device Sales, Time Management
Optional Skills
.
**Primary Work Location**
GBR Crawley
**Additional Locations**
**Work Shift**
At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You ( .
Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed.
The salary or hourly rate offered to a successful candidate is determined by their experience, education, and skills, as well as the labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location.
**Salary Range Information**
2,000.00 - 1,400.00 GBP Annual
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
Study Project Manager II Oncology
Posted 13 days ago
Job Viewed
Job Description
The Study Project Manager II Oncology drives the connection between the asset and operational delivery and execution of one or more clinical research studies. Leading the delivery of clinical operational strategies to ensure studies are executed with quality and efficiency, on-time, within budget, and meet company objectives. The Study Project Manager II achieves these objectives by bringing scientific acumen, strategic asset level thinking, innovation, expertise in clinical study operations management and stakeholder management to address risks and challenges.
Job Description
+ Defines and drives the study level operational strategies and deliverables - linking these to asset level goals
+ Brings strategic, asset level thinking and innovative problem solving to study planning and execution
+ Responsible for executing clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures).
+ Effectively present and contribute to discussions on study operations at asset level strategic meetings
+ Leads clinical operations planning through to execution via cross functional matrix environment and influences cross functional stakeholders to drive milestone achievement
+ Demonstrates the skills, experience and critical thinking to lead cross functional teams with minimal supervision.
+ Expertise in end-to-end clinical study operations management (all phases, set up to close out)
+ Coaches and mentors team members, delegates and empowers to the right level, actively contributes to Development Operations community
+ Demonstrates leadership with high level cross functional stakeholder management and influencing skills
+ Lead operational efficiencies and foster a culture of innovation
Qualifications
+ Bachelor's Degree or equivalent degree is required
+ Extensive demonstrated pharma-related and/or clinical research related experience or equivalent required.
+ Exposure in study initiation through study completion in Phase 1-4 and/or Medical Device Trial Experience.
+ No direct reports, but matrix management.
+ Required experience in Project Management interventional trials
+ Experience in Oncology studies in the last years of experience.
+ Homebased.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community? Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: