34 Oncology jobs in Leicestershire
Clinical Oncology Consultant
Derby, East Midlands
£60000 - £90000 annum
Hope Homecare Services Limited
Posted 148 days ago
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Job Description
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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.
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0
Clinical Research Scientist - Oncology
NG1 4GE Nottingham, East Midlands
£65000 Annually
WhatJobs
Posted 2 days ago
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Job Description
Our client, a cutting-edge biomedical research organization, is seeking a highly motivated and experienced Clinical Research Scientist specializing in Oncology to join their fully remote research and development team. This critical role will involve contributing to the design, execution, and analysis of groundbreaking clinical trials aimed at developing novel cancer therapies. You will be instrumental in translating preclinical findings into clinical applications and advancing our understanding of cancer biology and treatment. The position requires a deep scientific background, extensive experience in oncology research, and a passion for making a difference in patient lives. As part of a remote-first organization, you will collaborate virtually with a team of world-class scientists, clinicians, and statisticians. Key responsibilities include protocol development, data interpretation, scientific writing (publications, reports, regulatory submissions), and staying abreast of the latest scientific literature and technological advancements in oncology. You will critically evaluate research data, design experiments, and contribute to the strategic direction of our oncology pipeline. The ideal candidate will have a Ph.D. in a relevant biomedical science discipline (e.g., molecular biology, immunology, pharmacology) with a strong focus on cancer research. Proven experience in clinical trial design and execution, including knowledge of regulatory guidelines (e.g., ICH-GCP), is essential. Exceptional analytical, problem-solving, and communication skills are required, as is the ability to thrive in an independent, self-directed remote work environment. We are looking for a scientist who is not only technically proficient but also possesses strong scientific curiosity and a collaborative spirit. This is an unparalleled opportunity to contribute to transformative cancer research and development from the comfort of your home, working with leading experts in the field. Your insights will directly influence the trajectory of life-saving treatments and therapies. The role demands a high level of scientific rigor and ethical conduct, ensuring the integrity of all research activities. You will be a key player in bringing innovative solutions to patients facing cancer worldwide. This position offers significant opportunities for professional growth and the chance to be at the forefront of oncological advancements.
Responsibilities:
Responsibilities:
- Contribute to the design and execution of oncology clinical trials.
- Analyze and interpret complex clinical data, identifying key trends and insights.
- Author scientific publications, presentations, and regulatory documents.
- Collaborate with cross-functional teams, including medical affairs, statistics, and regulatory affairs.
- Stay current with scientific literature, emerging technologies, and competitive landscape in oncology.
- Provide scientific expertise and support for ongoing and planned clinical studies.
- Contribute to the strategic planning and development of the oncology pipeline.
- Ensure adherence to all relevant ethical and regulatory guidelines (e.g., ICH-GCP).
- Ph.D. in Molecular Biology, Immunology, Pharmacology, Oncology, or a related biomedical science.
- Minimum of 5 years of post-doctoral or industry experience in oncology drug development and clinical research.
- Strong understanding of cancer biology, mechanisms of action, and therapeutic strategies.
- Experience with clinical trial design, data analysis, and interpretation.
- Excellent scientific writing and presentation skills.
- Proficiency in statistical analysis software and data management tools is a plus.
- Demonstrated ability to work independently and collaboratively in a remote setting.
- Strong critical thinking, problem-solving, and organizational skills.
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1
Senior Clinical Research Scientist - Oncology
NG20 8UE Nottingham, East Midlands
£65000 Annually
WhatJobs
Posted 1 day ago
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Job Description
Our client, a leading global pharmaceutical company dedicated to improving patient lives, is seeking a highly experienced Senior Clinical Research Scientist with a specialization in Oncology. This role is based at their state-of-the-art research facility in Nottingham, Nottinghamshire, UK , and involves a hybrid working model to foster collaboration and flexibility.
Key Responsibilities:
Key Responsibilities:
- Lead the design, development, and execution of clinical trial protocols for oncology therapeutics, ensuring scientific rigor and regulatory compliance.
- Provide scientific and medical expertise throughout the clinical development process, from Phase I through Phase IV studies.
- Analyze and interpret complex clinical trial data, contributing to data reporting and scientific publications.
- Collaborate with cross-functional teams, including medical affairs, regulatory affairs, R&D, and clinical operations, to ensure successful trial conduct.
- Prepare scientific documents, such as Investigator Brochures, study reports, and regulatory submission documents.
- Engage with Key Opinion Leaders (KOLs) and investigators, presenting scientific data and insights.
- Oversee the selection of appropriate endpoints, biomarkers, and patient populations for clinical trials.
- Contribute to the development of new drug candidates and the strategic direction of the oncology pipeline.
- Stay abreast of the latest scientific advancements, clinical practices, and regulatory guidelines in oncology.
- Mentor junior scientists and contribute to the overall scientific growth of the clinical development team.
- PhD or MD degree in a relevant scientific or medical discipline (e.g., Oncology, Pharmacology, Medicine).
- A minimum of 5-7 years of progressive experience in clinical research within the pharmaceutical industry, with a strong focus on oncology drug development.
- In-depth knowledge of oncology, cancer biology, and relevant therapeutic areas.
- Proven experience in clinical trial design, protocol development, and data analysis.
- Strong understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements (FDA, EMA).
- Excellent scientific writing and communication skills, with a track record of publications and presentations.
- Strong analytical and problem-solving abilities.
- Ability to work effectively in a collaborative, cross-functional team environment.
- Experience in engaging with scientific and medical experts.
- Demonstrated ability to manage multiple complex projects simultaneously.
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2
Senior Clinical Research Scientist - Oncology
NG1 1GT Nottingham, East Midlands
£70000 Annually
WhatJobs
Posted 9 days ago
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Job Description
Our client, a global leader in pharmaceutical innovation, is looking for a dedicated and experienced Senior Clinical Research Scientist specializing in Oncology to join their fully remote team. This role is crucial for advancing cutting-edge cancer therapies through rigorous clinical trial design and execution. You will leverage your deep scientific expertise to contribute to groundbreaking research that aims to improve patient outcomes worldwide.
Key Responsibilities:
Qualifications and Experience:
This is an exceptional opportunity for a passionate Senior Clinical Research Scientist to make a significant impact on cancer treatment from a flexible, remote-first work environment.
Key Responsibilities:
- Design and develop innovative clinical trial protocols for novel oncology therapeutics, ensuring scientific validity and regulatory compliance.
- Provide scientific and clinical expertise throughout the lifecycle of clinical trials, from initial concept to final study report.
- Analyze and interpret complex clinical trial data, contributing to study conclusions and regulatory submissions.
- Collaborate with internal and external stakeholders, including investigators, key opinion leaders (KOLs), regulatory agencies, and project teams, to ensure successful trial conduct.
- Stay at the forefront of scientific advancements in oncology, including emerging therapeutic modalities, biomarkers, and treatment strategies.
- Contribute to the preparation of scientific publications, abstracts, and presentations.
- Ensure adherence to Good Clinical Practice (GCP), ethical standards, and all applicable regulatory guidelines.
- Review and provide input on Investigator's Brochures, clinical study reports, and regulatory submission documents.
- Mentor and guide junior scientists and clinical development team members.
- Participate in cross-functional team meetings and contribute to strategic decision-making for the oncology pipeline.
Qualifications and Experience:
- Advanced degree (M.D., Ph.D., Pharm.D.) in a life science or medical field, with a strong focus on oncology.
- Minimum of 5-7 years of direct experience in clinical research and development within the pharmaceutical or biotechnology industry, with a significant portion focused on oncology.
- Proven track record in designing and executing Phase I, II, and III clinical trials for cancer therapeutics.
- In-depth knowledge of oncology disease areas, treatment paradigms, and relevant biomarkers.
- Familiarity with global regulatory requirements (e.g., FDA, EMA) and ICH-GCP guidelines.
- Excellent scientific writing, analytical, and presentation skills.
- Demonstrated ability to work independently and effectively manage multiple priorities in a remote setting.
- Strong collaborative skills and experience working with multidisciplinary teams.
- Proficiency in data analysis and interpretation.
This is an exceptional opportunity for a passionate Senior Clinical Research Scientist to make a significant impact on cancer treatment from a flexible, remote-first work environment.
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3
Senior Clinical Research Associate - Oncology
LE1 5XX Leicester, East Midlands
£55000 Annually
WhatJobs
Posted 12 days ago
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Our client is seeking a highly motivated and experienced Senior Clinical Research Associate (CRA) to join their dynamic pharmaceutical team. This is a fully remote position, offering the flexibility to work from anywhere within the UK. You will play a pivotal role in overseeing clinical trials, ensuring compliance with all regulatory standards and protocols. The role focuses heavily on oncology studies, demanding a deep understanding of cancer treatments and trial methodologies.
Key Responsibilities:
Key Responsibilities:
- Conduct site initiation, monitoring, and close-out visits for clinical trial sites.
- Ensure adherence to Good Clinical Practice (GCP), FDA regulations, and other relevant guidelines.
- Manage multiple clinical trial sites simultaneously, fostering strong relationships with investigators and site staff.
- Oversee data collection, accuracy, and integrity, resolving any discrepancies promptly.
- Prepare and present study progress reports to internal stakeholders and regulatory bodies.
- Manage investigational product accountability and drug supply at trial sites.
- Identify and report adverse events and serious adverse events in a timely manner.
- Contribute to the development of clinical trial protocols and Case Report Forms (CRFs).
- Mentor and support junior CRAs, sharing expertise and best practices.
- Act as a key liaison between the sponsor, investigational sites, and the clinical operations team.
- Bachelor's degree in a life science, nursing, pharmacy, or related discipline. Advanced degree preferred.
- Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical industry, with a strong emphasis on oncology.
- Proven track record of successfully managing complex clinical trials.
- Extensive knowledge of ICH-GCP guidelines and regulatory requirements.
- Excellent communication, interpersonal, and organizational skills.
- Ability to work independently and manage time effectively in a remote setting.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Willingness to travel to sites occasionally for essential on-site visits, although the role is primarily remote.
- Demonstrated ability to problem-solve and make sound decisions under pressure.
- A passion for advancing cancer research and improving patient outcomes.
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4
Senior Clinical Research Scientist, Oncology
LE2 7JL Leicester, East Midlands
£80000 Annually
WhatJobs
Posted 12 days ago
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Job Description
Our client, a pioneering pharmaceutical company dedicated to advancing global health, is seeking an exceptional Senior Clinical Research Scientist specializing in Oncology. This is a fully remote position, offering the flexibility to contribute from anywhere within the UK. You will play a pivotal role in the design, execution, and interpretation of clinical trials for novel cancer therapeutics. This role demands a deep scientific understanding, robust analytical skills, and a commitment to rigorous research standards. You will collaborate with cross-functional teams, including R&D, regulatory affairs, and medical affairs, to ensure the successful progression of clinical development programs. The ideal candidate will possess a strong publication record and a proven ability to translate scientific insights into actionable clinical strategies. We are looking for a proactive individual who can independently drive research projects and contribute to the company's pipeline.
Key Responsibilities:
Key Responsibilities:
- Design and develop clinical trial protocols for oncology indications, ensuring scientific rigor and regulatory compliance.
- Oversee the planning and execution of clinical studies, including site selection, investigator engagement, and data collection.
- Analyze and interpret clinical trial data, preparing comprehensive reports and presentations for internal stakeholders and regulatory bodies.
- Contribute to the development of scientific strategy and lifecycle management for assigned compounds.
- Collaborate closely with internal teams (e.g., biostatistics, data management, regulatory affairs) and external partners (e.g., CROs, investigators).
- Stay abreast of the latest scientific advancements and competitive landscape in oncology drug development.
- Contribute to the preparation of manuscripts for publication and presentations at scientific conferences.
- Provide scientific guidance and support to clinical operations and medical affairs teams.
- Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Pharmacology, Molecular Biology).
- Minimum of 5-7 years of experience in clinical research within the pharmaceutical or biotechnology industry, with a focus on oncology.
- Demonstrated expertise in clinical trial design, execution, and data analysis.
- Strong understanding of oncology drug development pathways and regulatory requirements (e.g., FDA, EMA).
- Excellent scientific writing and communication skills, with a proven ability to publish research findings.
- Experience working in a remote or hybrid environment is advantageous.
- Ability to work independently and collaboratively in a fast-paced, global team setting.
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5
Senior Clinical Research Scientist - Oncology
CV3 5GU Coventry, West Midlands
£60000 Annually
WhatJobs
Posted 12 days ago
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Job Description
Our client, a leading entity in the pharmaceutical sector, is seeking a highly motivated and experienced Senior Clinical Research Scientist to join their innovative team in Coventry, West Midlands, UK . This is a crucial role responsible for the design, execution, and analysis of clinical trials, with a specific focus on oncology treatments. You will be instrumental in advancing novel therapies from early-stage research through to late-stage development, ensuring compliance with all regulatory standards and ethical guidelines.
Responsibilities:
Responsibilities:
- Design and develop clinical trial protocols, ensuring scientific rigor and feasibility.
- Oversee the day-to-day operations of clinical studies, managing timelines and budgets effectively.
- Collaborate with cross-functional teams, including medical affairs, regulatory affairs, and project management, to ensure seamless trial execution.
- Analyze and interpret complex clinical data, preparing comprehensive study reports and publications.
- Liaise with investigators, site staff, and key opinion leaders to foster strong working relationships.
- Ensure all clinical research activities are conducted in strict adherence to Good Clinical Practice (GCP) and relevant regulatory requirements (e.g., MHRA, FDA).
- Contribute to the development of scientific strategies and identify new research opportunities.
- Mentor and guide junior research staff, fostering a culture of scientific excellence and continuous improvement.
- Prepare and present research findings at scientific meetings and conferences.
- Manage external collaborations with academic institutions and contract research organizations (CROs).
- Ph.D. or M.Sc. in a relevant life science discipline (e.g., Pharmacology, Biology, Biochemistry, Medicine).
- Minimum of 5-7 years of progressive experience in clinical research within the pharmaceutical industry or a closely related field.
- Proven track record in designing and managing oncology clinical trials.
- In-depth knowledge of drug development processes, clinical trial methodology, and regulatory affairs.
- Strong analytical and problem-solving skills, with the ability to interpret complex datasets.
- Excellent written and verbal communication skills, with a demonstrated ability to publish scientific findings.
- Proficiency in statistical analysis software is advantageous.
- Experience with project management tools and techniques.
- Ability to work independently and collaboratively in a fast-paced environment.
- Strong leadership potential and a passion for scientific innovation.
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6
Senior Clinical Research Scientist - Oncology
CV1 2GN Coventry, West Midlands
£65000 annum + bon
WhatJobs
Posted 12 days ago
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Job Description
Our client, a globally recognised pharmaceutical company renowned for its commitment to innovative therapies, is seeking a highly motivated Senior Clinical Research Scientist specializing in Oncology. This hybrid role offers a dynamic working environment within their state-of-the-art research facilities in Coventry, West Midlands , combined with the flexibility of remote work. You will play a critical role in the design, execution, and interpretation of clinical trials for novel cancer treatments. This position requires a deep understanding of oncology drug development, clinical trial methodologies, and regulatory requirements. The ideal candidate will possess strong scientific acumen, excellent data analysis skills, and the ability to collaborate effectively with multidisciplinary teams.
Key Responsibilities:
Key Responsibilities:
- Lead the scientific design and strategy for Phase I-IV clinical trials in oncology.
- Develop clinical trial protocols, study plans, and informed consent forms.
- Oversee the operational execution of clinical trials, ensuring compliance with GCP and regulatory guidelines.
- Collaborate with investigators, clinical research associates (CRAs), and study site personnel.
- Analyse and interpret clinical trial data, including efficacy, safety, and biomarker endpoints.
- Prepare clinical study reports (CSRs), regulatory submissions, and publications.
- Contribute to the development of research strategies and therapeutic area plans.
- Evaluate new scientific literature and emerging research to identify potential drug candidates and trial opportunities.
- Manage relationships with key opinion leaders (KOLs) and external scientific advisors.
- Present scientific findings at internal meetings, advisory boards, and scientific conferences.
- Provide scientific and technical expertise to cross-functional teams, including regulatory affairs, medical affairs, and R&D.
- Contribute to the safety monitoring and risk management of clinical trials.
- PhD or MD in a relevant scientific discipline (e.g., Oncology, Pharmacology, Biology).
- Minimum of 5 years' experience in clinical research, with a significant focus on oncology drug development.
- In-depth knowledge of cancer biology, therapeutic targets, and clinical trial methodologies.
- Proven experience in protocol development, clinical trial management, and data analysis.
- Familiarity with ICH-GCP guidelines and regulatory submission processes (e.g., FDA, EMA).
- Strong scientific writing and presentation skills.
- Excellent analytical and problem-solving abilities.
- Ability to work independently and effectively within a collaborative team structure.
- Proficiency in clinical data management systems and statistical software is advantageous.
- Strong communication and interpersonal skills.
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7
Senior Clinical Research Associate - Oncology
NG1 1HN Nottingham, East Midlands
£50000 Annually
WhatJobs
Posted 12 days ago
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Job Description
Our client, a leading global pharmaceutical company dedicated to advancing healthcare, is seeking an experienced Senior Clinical Research Associate (CRA) to join their vital oncology team. This role offers a hybrid working model, combining the benefits of remote work with essential on-site collaboration at their facilities in Nottingham, Nottinghamshire, UK . You will play a critical role in managing and conducting clinical trials, ensuring data integrity, patient safety, and compliance with regulatory standards.
As a Senior CRA, you will be responsible for site selection, initiation, monitoring, and close-out visits for clinical trial sites. Your expertise will be crucial in overseeing study progress, ensuring adherence to protocols and Good Clinical Practice (GCP) guidelines. You will serve as the primary liaison between study sites, internal study teams, and regulatory authorities, contributing significantly to the successful development of life-saving oncology treatments.
Key Responsibilities:
As a Senior CRA, you will be responsible for site selection, initiation, monitoring, and close-out visits for clinical trial sites. Your expertise will be crucial in overseeing study progress, ensuring adherence to protocols and Good Clinical Practice (GCP) guidelines. You will serve as the primary liaison between study sites, internal study teams, and regulatory authorities, contributing significantly to the successful development of life-saving oncology treatments.
Key Responsibilities:
- Conduct site selection, initiation, interim monitoring, and close-out visits in accordance with study protocols and SOPs.
- Assess protocol and regulatory compliance at clinical trial sites through review of essential documents and patient records.
- Ensure the safety of study participants and the integrity of the data collected.
- Manage communication and relationships with principal investigators and site staff.
- Identify, evaluate, and implement corrective and preventive actions (CAPAs) for site-related issues.
- Train and mentor junior CRAs and study site personnel on study-specific procedures and GCP.
- Oversee study timelines and milestones, ensuring timely progress and efficient resource utilization.
- Prepare and present monitoring visit reports, highlighting findings and recommendations.
- Ensure all study documentation is maintained accurately and in a timely manner within the required systems.
- Collaborate with cross-functional teams, including project managers, medical monitors, and data managers.
- Stay current with industry regulations, guidelines, and best practices in clinical research.
- Bachelor's degree in a life science, nursing, pharmacy, or a related discipline. Advanced degree is a plus.
- Minimum of 5 years of direct experience as a Clinical Research Associate in the pharmaceutical or biotech industry.
- Proven experience in managing oncology clinical trials is essential.
- Thorough understanding of ICH-GCP guidelines, regulatory requirements (FDA, EMA), and clinical trial processes.
- Demonstrated ability to effectively monitor multiple clinical trial sites.
- Excellent organisational, time management, and problem-solving skills.
- Strong written and verbal communication skills, with the ability to build rapport and influence effectively.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently and as part of a collaborative team in a hybrid work environment.
- Commitment to patient safety and data quality.
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8
Clinical Research Associate (CRA) - Oncology
LE1 5BE Leicester, East Midlands
£45000 Annually
WhatJobs
Posted 12 days ago
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Our client is seeking a dedicated and experienced Clinical Research Associate (CRA) with a specialization in Oncology to join their growing clinical development team. This crucial role involves overseeing and managing clinical trials to ensure they are conducted, recorded, and reported in accordance with protocol, standard operating procedures, and all applicable regulations. The CRA will be responsible for site selection, initiation, monitoring, and close-out visits, ensuring data integrity and patient safety.
Key responsibilities include conducting pre-study, initiation, routine monitoring, and close-out visits to investigational sites; assessing protocol and regulatory compliance; and identifying, resolving, or escalating site issues. You will be responsible for maintaining accurate and complete trial documentation, including trial master files (TMFs). The ideal candidate will possess a strong understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements specific to pharmaceutical drug development. Excellent communication, organizational, and problem-solving skills are essential, as is the ability to build strong working relationships with investigators, site staff, and internal project teams.
This is a hybrid role, requiring a blend of remote work and frequent site visits within the designated region, including travel to our client's facility near **Leicester, Leicestershire, UK**. A Bachelor's degree in a life science, nursing, or a related field is required. A minimum of 2-3 years of experience as a CRA, with a significant focus on oncology trials, is essential. Strong knowledge of ICH-GCP guidelines and experience with various EDC systems are mandatory. The ability to travel regionally is a requirement. This is an excellent opportunity for a motivated CRA to contribute to the development of life-saving cancer treatments within a supportive and innovative environment.
Key responsibilities include conducting pre-study, initiation, routine monitoring, and close-out visits to investigational sites; assessing protocol and regulatory compliance; and identifying, resolving, or escalating site issues. You will be responsible for maintaining accurate and complete trial documentation, including trial master files (TMFs). The ideal candidate will possess a strong understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements specific to pharmaceutical drug development. Excellent communication, organizational, and problem-solving skills are essential, as is the ability to build strong working relationships with investigators, site staff, and internal project teams.
This is a hybrid role, requiring a blend of remote work and frequent site visits within the designated region, including travel to our client's facility near **Leicester, Leicestershire, UK**. A Bachelor's degree in a life science, nursing, or a related field is required. A minimum of 2-3 years of experience as a CRA, with a significant focus on oncology trials, is essential. Strong knowledge of ICH-GCP guidelines and experience with various EDC systems are mandatory. The ability to travel regionally is a requirement. This is an excellent opportunity for a motivated CRA to contribute to the development of life-saving cancer treatments within a supportive and innovative environment.
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