Explore opportunities in cancer research, a field dedicated to understanding, preventing, and treating cancer. Professionals in this area work across various disciplines, including biology, genetics, and medicine, to advance scientific knowledge and develop innovative therapies. Cancer research jobs involve laboratory work, clinical trials, data analysis, and scientific writing, contributing to improved patient outcomes and public health.6,985 Cancer Research jobs in the United Kingdom
Clinical Research Scientist
M1 1AE Manchester, North West
£50000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is seeking a talented Clinical Research Scientist to join their dynamic team in **Manchester, Greater Manchester, UK**. This hybrid role offers a unique opportunity to contribute to groundbreaking research and development in a collaborative and cutting-edge environment. You will play a pivotal role in the design, execution, and analysis of clinical trials, ensuring adherence to regulatory guidelines and scientific rigor. Your responsibilities will include developing clinical trial protocols, study plans, and informed consent forms, ensuring all documentation meets high scientific and ethical standards. You will manage the operational aspects of clinical trials, including site selection, initiation, monitoring, and close-out, working closely with clinical research associates and site staff. Data analysis and interpretation will be a key component of your role, involving the evaluation of study results, statistical analysis, and the preparation of comprehensive reports for regulatory submissions and publications. You will collaborate with cross-functional teams, including biostatistics, data management, regulatory affairs, and medical affairs, to ensure seamless trial progression. Staying abreast of scientific literature, emerging trends, and competitive intelligence within the pharmaceutical landscape is crucial.
The ideal candidate will hold a PhD or Master's degree in a relevant life science discipline (e.g., Pharmacology, Biology, Medicine) with a strong foundation in clinical research methodologies. You should have demonstrable experience in clinical trial management, including protocol development and study execution, within the pharmaceutical or biotechnology sector. A thorough understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements (e.g., EMA, FDA) is essential. Excellent analytical, problem-solving, and communication skills are required, along with the ability to present complex scientific information clearly and concisely. Experience with statistical analysis software and data visualization tools is advantageous. While this role is primarily based in our Manchester office, a hybrid work model allows for a balanced approach to on-site collaboration and remote work, offering flexibility for the right candidate.
The ideal candidate will hold a PhD or Master's degree in a relevant life science discipline (e.g., Pharmacology, Biology, Medicine) with a strong foundation in clinical research methodologies. You should have demonstrable experience in clinical trial management, including protocol development and study execution, within the pharmaceutical or biotechnology sector. A thorough understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements (e.g., EMA, FDA) is essential. Excellent analytical, problem-solving, and communication skills are required, along with the ability to present complex scientific information clearly and concisely. Experience with statistical analysis software and data visualization tools is advantageous. While this role is primarily based in our Manchester office, a hybrid work model allows for a balanced approach to on-site collaboration and remote work, offering flexibility for the right candidate.
This advertiser has chosen not to accept applicants from your region.
0
Clinical Research Scientist
PL1 2AB Plymouth, South West
£60000 Annually
WhatJobs
Posted 15 days ago
Job Viewed
Job Description
Our client is a leading pharmaceutical innovator seeking a highly skilled and motivated Clinical Research Scientist to join their globally distributed, remote-first team. This pivotal role focuses on designing, implementing, and overseeing clinical trial protocols that drive groundbreaking therapeutic advancements. You will be instrumental in bringing life-changing medicines to patients, contributing significantly to the drug development lifecycle from early phase studies through to post-market surveillance. This is an exceptional opportunity for an experienced scientist to leverage their expertise in a fully remote capacity, shaping the future of healthcare.
Responsibilities:
Qualifications:
This role is entirely remote, offering the flexibility to work from any approved location. We provide a comprehensive remote onboarding process and ensure our team members have the tools and support needed to excel. Join a forward-thinking company dedicated to making a real difference.
Responsibilities:
- Design and develop clinical trial protocols, ensuring scientific rigor, regulatory compliance, and alignment with study objectives.
- Oversee the execution of clinical trials, providing scientific and operational guidance to study teams.
- Analyze and interpret complex clinical data, drawing meaningful conclusions and preparing comprehensive study reports.
- Collaborate closely with cross-functional teams, including regulatory affairs, data management, biostatistics, and medical affairs.
- Contribute to the development of Investigator's Brochures, study manuals, and other essential study documents.
- Monitor study progress, identify potential issues, and implement corrective actions to ensure timely and high-quality trial completion.
- Stay current with scientific literature, emerging technologies, and regulatory guidelines relevant to clinical research.
- Present study findings at scientific meetings and contribute to publications in peer-reviewed journals.
- Manage relationships with external partners, including investigators, research sites, and contract research organizations (CROs).
- Ensure adherence to Good Clinical Practice (GCP) and other applicable regulatory standards.
- Provide scientific input into portfolio strategy and target product profiles.
- Evaluate potential new drug candidates and therapeutic areas for clinical development.
Qualifications:
- PhD or equivalent advanced degree in Life Sciences, Pharmacology, Medicine, or a related field.
- Minimum of 6-8 years of progressive experience in clinical research, with a strong focus on drug development within the pharmaceutical or biotechnology industry.
- Demonstrated success in designing and executing clinical trials across various therapeutic areas.
- Expertise in clinical data analysis, interpretation, and reporting.
- Thorough understanding of ICH guidelines, GCP, and relevant regulatory requirements (e.g., FDA, EMA).
- Excellent scientific writing and presentation skills.
- Proven ability to work effectively in a remote, collaborative, and international team environment.
- Strong project management and organizational skills.
- Experience with statistical analysis and interpretation of clinical trial data.
- Proficiency in using clinical trial management systems and electronic data capture (EDC) systems.
- Ability to critically evaluate scientific literature and data.
- A passion for innovation and improving patient outcomes.
This role is entirely remote, offering the flexibility to work from any approved location. We provide a comprehensive remote onboarding process and ensure our team members have the tools and support needed to excel. Join a forward-thinking company dedicated to making a real difference.
This advertiser has chosen not to accept applicants from your region.
1
Clinical Research Scientist
NG1 1GG Nottingham, East Midlands
£55000 Annually
WhatJobs
Posted 24 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company dedicated to advancing global health, is looking for a highly skilled and motivated Clinical Research Scientist to join their esteemed research and development team based in Nottingham, Nottinghamshire, UK . This critical role involves contributing to the design, execution, and analysis of clinical trials for novel therapeutic agents. You will be responsible for the scientific integrity of clinical studies, ensuring compliance with regulatory requirements and ethical standards. Key duties include developing clinical protocols, managing data collection and analysis, interpreting study results, and preparing scientific reports and publications. You will collaborate closely with internal teams, including R&D, regulatory affairs, and medical affairs, as well as external stakeholders such as investigators, ethics committees, and contract research organizations (CROs). The ideal candidate will possess a Ph.D. or Master's degree in a relevant life science discipline (e.g., pharmacology, biology, medicine) with significant experience in clinical research within the pharmaceutical industry. A strong understanding of drug development processes, Good Clinical Practice (GCP) guidelines, and regulatory frameworks (e.g., FDA, EMA) is essential. Excellent scientific writing, communication, and interpersonal skills are required to effectively present complex data and engage with diverse audiences. This is an exciting opportunity to contribute to the development of life-changing medicines and advance your career in a dynamic and supportive environment. The role requires presence in our Nottingham facility to facilitate essential in-person collaboration and laboratory work.
This advertiser has chosen not to accept applicants from your region.
2
Clinical Research Scientist
CF10 1DA Cardiff, Wales
£60000 Annually
WhatJobs
Posted 24 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company committed to improving global health, is seeking a dedicated and experienced Clinical Research Scientist to join their dynamic team in **Cardiff**, Wales. This role is integral to the design, execution, and interpretation of clinical trials for novel therapeutic agents. You will play a key part in bringing life-changing medicines to patients by ensuring the highest standards of scientific integrity and regulatory compliance throughout the clinical development process. The ideal candidate will possess a strong scientific background, extensive experience in clinical trial management, and a deep understanding of regulatory guidelines (e.g., ICH-GCP). Responsibilities include developing clinical trial protocols, overseeing study conduct, managing data analysis and interpretation, and preparing regulatory submissions. You will collaborate closely with internal teams, including R&D, regulatory affairs, and project management, as well as external partners such as investigators, site staff, and contract research organizations (CROs). This position requires exceptional analytical, problem-solving, and communication skills, as well as the ability to work effectively in a collaborative, fast-paced environment. This role is office-based in **Cardiff**. We offer a competitive salary, comprehensive benefits package, and opportunities for professional growth and development within a company that values innovation and scientific excellence.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Design and develop clinical trial protocols in accordance with scientific objectives and regulatory requirements.
- Oversee the execution of clinical trials, ensuring compliance with ICH-GCP and other relevant regulations.
- Manage study timelines, budgets, and resources effectively.
- Collaborate with investigators and clinical site staff to ensure high-quality data collection.
- Analyze and interpret clinical trial data, contributing to study reports and publications.
- Prepare study-related documents, including investigator brochures, case report forms, and regulatory submission dossiers.
- Liaise with regulatory authorities and ethics committees.
- Contribute to the scientific strategy for drug development programs.
- Mentor and guide junior research staff.
Qualifications:
- PhD or Master's degree in Life Sciences, Pharmacy, Medicine, or a related field.
- Minimum of 5 years of experience in clinical research and development within the pharmaceutical industry.
- Thorough understanding of clinical trial design, execution, and data analysis.
- In-depth knowledge of ICH-GCP guidelines and regulatory submission processes.
- Excellent scientific writing, analytical, and problem-solving skills.
- Strong interpersonal and communication skills, with the ability to build effective relationships.
- Experience in (Specific Therapeutic Area, e.g., Oncology, Cardiology) is a plus.
- Proficiency in relevant clinical trial management systems and statistical software.
This advertiser has chosen not to accept applicants from your region.
3
Clinical Research Scientist (Oncology)
PO1 1AA Portsmouth, South East
£50000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly skilled Clinical Research Scientist specializing in Oncology to join their dedicated team. This role offers a unique opportunity to contribute to the development of life-saving therapies, working within a hybrid model that balances essential in-office collaboration with remote flexibility. You will play a crucial role in the design, execution, and analysis of clinical trials, ensuring the highest standards of scientific integrity and regulatory compliance. The ideal candidate possesses a deep understanding of oncology drug development, strong analytical capabilities, and a passion for advancing patient care.
Key Responsibilities:
Qualifications:
This hybrid role offers the flexibility of remote work combined with essential in-office collaboration, based at our client's facility in Portsmouth, Hampshire, UK . Join a team dedicated to making a significant difference in the lives of cancer patients worldwide.
Key Responsibilities:
- Design and develop clinical trial protocols for oncology indications, ensuring scientific validity and alignment with strategic objectives.
- Oversee the operational aspects of clinical trials, including site selection, investigator training, and data monitoring.
- Analyze and interpret complex clinical trial data, preparing comprehensive reports for regulatory submissions and internal stakeholders.
- Collaborate closely with cross-functional teams, including R&D, regulatory affairs, medical affairs, and project management.
- Ensure adherence to Good Clinical Practice (GCP) guidelines and all relevant regulatory requirements.
- Evaluate and present scientific findings at internal meetings, advisory boards, and external conferences.
- Contribute to the development of new drug candidates and the optimization of existing treatments.
- Manage relationships with external investigators, key opinion leaders, and contract research organizations (CROs).
- Stay abreast of the latest advancements in oncology research, clinical trial methodologies, and regulatory landscapes.
- Contribute to the scientific and strategic direction of the oncology pipeline.
Qualifications:
- Ph.D. or M.D. in a relevant scientific or medical field, with a strong focus on oncology.
- Minimum of 5 years of experience in clinical research, preferably within the pharmaceutical industry.
- Demonstrated expertise in designing, conducting, and analyzing Phase I-III clinical trials for oncology drugs.
- In-depth knowledge of oncology biology, disease mechanisms, and therapeutic strategies.
- Familiarity with regulatory requirements (FDA, EMA) and ICH/GCP guidelines.
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong written and verbal communication skills, with the ability to present complex scientific information clearly.
- Experience in managing external collaborations and CROs.
- Ability to work effectively in a hybrid work environment, balancing remote and in-office responsibilities.
- A proactive approach and a passion for contributing to groundbreaking medical advancements.
This hybrid role offers the flexibility of remote work combined with essential in-office collaboration, based at our client's facility in Portsmouth, Hampshire, UK . Join a team dedicated to making a significant difference in the lives of cancer patients worldwide.
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Scientist (Oncology)
M17 8 Manchester, North West
£55000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
A leading pharmaceutical company based in Manchester, Greater Manchester, UK , is seeking a highly motivated and experienced Clinical Research Scientist specializing in Oncology to join their innovative research and development team. This is a Hybrid role, combining the flexibility of remote work with the collaborative environment of our state-of-the-art facility. You will play a critical role in the design, execution, and interpretation of clinical trials for novel cancer therapies.
Responsibilities include developing clinical trial protocols, selecting and managing clinical sites, overseeing data collection and analysis, and ensuring compliance with regulatory guidelines (e.g., GCP, ICH). You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and project management, to drive research objectives forward. The ideal candidate will have a strong scientific background with expertise in oncology drug development. You will be involved in identifying potential patient populations, assessing drug safety and efficacy, and contributing to regulatory submissions. This position demands meticulous attention to detail, exceptional analytical skills, and the ability to communicate complex scientific information effectively.
Qualifications include a PhD or Master's degree in Life Sciences, Pharmacy, Medicine, or a related discipline, with a minimum of 3-5 years of experience in clinical research within the pharmaceutical or biotech industry, specifically in oncology. Proven experience in designing and managing Phase I-III clinical trials is essential. Knowledge of cancer biology, therapeutic targets, and current treatment landscapes is required. Excellent written and verbal communication skills, strong project management abilities, and the capacity to work independently as well as part of a collaborative team are crucial. You should be adept at interpreting clinical data, preparing scientific reports, and presenting findings to internal and external stakeholders. This role offers a unique opportunity to contribute to the development of life-saving treatments and advance your career in a rapidly growing field.
Responsibilities include developing clinical trial protocols, selecting and managing clinical sites, overseeing data collection and analysis, and ensuring compliance with regulatory guidelines (e.g., GCP, ICH). You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and project management, to drive research objectives forward. The ideal candidate will have a strong scientific background with expertise in oncology drug development. You will be involved in identifying potential patient populations, assessing drug safety and efficacy, and contributing to regulatory submissions. This position demands meticulous attention to detail, exceptional analytical skills, and the ability to communicate complex scientific information effectively.
Qualifications include a PhD or Master's degree in Life Sciences, Pharmacy, Medicine, or a related discipline, with a minimum of 3-5 years of experience in clinical research within the pharmaceutical or biotech industry, specifically in oncology. Proven experience in designing and managing Phase I-III clinical trials is essential. Knowledge of cancer biology, therapeutic targets, and current treatment landscapes is required. Excellent written and verbal communication skills, strong project management abilities, and the capacity to work independently as well as part of a collaborative team are crucial. You should be adept at interpreting clinical data, preparing scientific reports, and presenting findings to internal and external stakeholders. This role offers a unique opportunity to contribute to the development of life-saving treatments and advance your career in a rapidly growing field.
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Scientist - Oncology
PL1 2LU Plymouth, South West
£50000 Annually
WhatJobs
Posted 8 days ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical company, is seeking a dedicated and experienced Clinical Research Scientist specializing in Oncology to join their esteemed research and development team in Plymouth, Devon, UK . This critical role will focus on the design, implementation, and management of clinical trials for novel oncology therapeutics. The successful candidate will play a key role in advancing our understanding of cancer treatments and bringing life-saving medications to patients. Responsibilities include developing clinical trial protocols, overseeing patient recruitment, managing data integrity, and ensuring compliance with regulatory guidelines (e.g., GCP, ICH). You will collaborate closely with investigators, site staff, and internal cross-functional teams, including medical affairs, regulatory affairs, and project management. A strong understanding of oncology, including various cancer types, treatment modalities, and current research trends, is essential. Experience in analyzing clinical trial data, interpreting results, and contributing to scientific publications and regulatory submissions is highly desirable. The ideal candidate possesses excellent scientific acumen, meticulous attention to detail, and superior organizational and communication skills. This position offers a unique opportunity to contribute to groundbreaking research in a challenging and rewarding field. The role demands a commitment to scientific excellence and a passion for improving patient outcomes. You will be instrumental in shaping the clinical development strategy for our pipeline assets. Join a forward-thinking organization dedicated to making a real difference in the lives of cancer patients worldwide. The role is based at our facilities in Plymouth, Devon, UK , offering a stimulating work environment with opportunities for professional growth and development. This is a hands-on role requiring active participation in all phases of clinical trial execution.
Responsibilities:
Responsibilities:
- Develop and write clinical trial protocols and amendments.
- Contribute to the design and planning of Phase I-IV clinical trials in oncology.
- Monitor clinical trial progress and ensure adherence to protocols and regulatory requirements.
- Manage relationships with clinical investigators and site personnel.
- Oversee data collection, quality control, and analysis of clinical trial data.
- Contribute to the preparation of clinical study reports, scientific publications, and regulatory submissions.
- Provide scientific and clinical input to other functional areas.
- Stay updated on the latest scientific advancements and competitive landscape in oncology.
- Participate in the selection and management of external vendors and partners.
- Ensure ethical conduct and patient safety throughout the trial lifecycle.
- PhD or MSc in a life science discipline (e.g., Biology, Biochemistry, Pharmacology, Medicine).
- Minimum of 5 years of experience in clinical research, with a significant focus on oncology drug development.
- In-depth knowledge of oncology, clinical trial design, and regulatory requirements.
- Strong understanding of Good Clinical Practice (GCP) and ICH guidelines.
- Proven ability to analyze and interpret clinical data.
- Excellent written and verbal communication skills.
- Ability to manage multiple projects and prioritize effectively.
- Strong interpersonal skills and ability to work collaboratively in a team environment.
This advertiser has chosen not to accept applicants from your region.
Be The First To Know
About the latest Cancer research Jobs in United Kingdom !
6
Clinical Research Scientist - Oncology
NE1 1 Newcastle upon Tyne, North East
£55000 Annually
WhatJobs
Posted 8 days ago
Job Viewed
Job Description
Our client, a pioneering pharmaceutical company, is seeking an exceptional Clinical Research Scientist specializing in Oncology to join their innovative R&D team based near Newcastle upon Tyne, Tyne and Wear, UK . This hybrid role offers the best of both worlds, combining essential on-site collaboration with the flexibility of remote work. You will be instrumental in designing, conducting, and analyzing clinical trials for novel cancer therapies, contributing significantly to the advancement of patient care. The ideal candidate will possess a strong scientific background, a deep understanding of oncology drug development, and a passion for cutting-edge research.
Key Responsibilities:
Key Responsibilities:
- Design and develop clinical trial protocols for oncology therapeutics, ensuring scientific rigor and regulatory compliance.
- Oversee the execution of clinical trials, including site selection, investigator meetings, and monitoring trial progress.
- Analyze and interpret complex clinical data, preparing comprehensive reports and scientific publications.
- Collaborate with cross-functional teams, including medical affairs, regulatory affairs, and project management, to ensure seamless trial operations.
- Identify and evaluate potential drug targets and biomarkers for new oncology treatments.
- Contribute to the preparation of regulatory submissions (e.g., IND, NDA).
- Stay abreast of the latest advancements in oncology, clinical research methodologies, and pharmaceutical regulations.
- Present research findings at scientific conferences and internal meetings.
- Mentor junior research staff and contribute to the development of the research team.
- Ensure adherence to Good Clinical Practice (GCP) and other relevant ethical guidelines.
- Ph.D. or M.D. in a relevant life science discipline (e.g., Oncology, Pharmacology, Molecular Biology).
- Minimum of 4-6 years of experience in clinical research, with a focus on oncology drug development.
- Proven track record in designing and managing complex clinical trials.
- In-depth knowledge of cancer biology, therapeutic modalities, and current treatment landscape.
- Experience with statistical analysis of clinical data and familiarity with biostatistics principles.
- Excellent scientific writing and presentation skills.
- Strong understanding of regulatory requirements (FDA, EMA) and GCP guidelines.
- Ability to work effectively in a collaborative, cross-functional team environment.
- Experience with hybrid work models and proficient in remote collaboration tools.
- Demonstrated ability to think critically and solve complex scientific problems.
This advertiser has chosen not to accept applicants from your region.
7
Clinical Research Scientist (Oncology)
WV1 1AB Wolverhampton, West Midlands
£55000 Annually
WhatJobs
Posted 12 days ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical company, is seeking an accomplished Clinical Research Scientist specializing in Oncology to join their dedicated research team based in **Wolverhampton, West Midlands, UK**. This is a vital on-site role focused on the design, execution, and monitoring of clinical trials for innovative oncology therapeutics. The successful candidate will play a crucial part in bringing life-changing treatments to patients by ensuring trials are conducted ethically, efficiently, and in compliance with global regulatory standards. You will work closely with investigators, clinical research associates, and internal stakeholders to manage all aspects of clinical trial operations.
Key Responsibilities:
Key Responsibilities:
- Contribute to the development of clinical trial protocols and study designs for oncology indications.
- Oversee the initiation, conduct, and completion of clinical trials at assigned investigational sites.
- Ensure adherence to Good Clinical Practice (GCP), regulatory requirements, and company SOPs.
- Manage relationships with investigators, site staff, and contract research organizations (CROs).
- Monitor trial progress, data quality, and patient safety, implementing corrective actions as needed.
- Review and interpret clinical data, preparing reports on study progress and outcomes.
- Collaborate with medical affairs, regulatory affairs, and R&D teams to ensure seamless trial management.
- Contribute to the preparation of regulatory submissions and scientific publications.
- Identify and assess potential risks and develop mitigation strategies for clinical trials.
- Provide scientific and operational guidance to clinical research associates (CRAs) and other study personnel.
- Maintain accurate and comprehensive trial documentation.
- Participate in site selection and initiation visits.
- Ph.D. or Master's degree in Life Sciences, Pharmacy, Medicine, or a related field.
- Minimum of 5 years of experience in clinical research, with a significant focus on oncology trials.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Proven experience in managing clinical trials from protocol development through to final study report.
- Excellent understanding of oncology, including disease states, therapeutic approaches, and drug development processes.
- Strong project management and organizational skills.
- Exceptional communication, interpersonal, and negotiation skills.
- Ability to work effectively under pressure and manage multiple priorities.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Willingness to travel to clinical sites as required.
This advertiser has chosen not to accept applicants from your region.
8
Clinical Research Scientist - Oncology
NG1 4GE Nottingham, East Midlands
£65000 Annually
WhatJobs
Posted 14 days ago
Job Viewed
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.
This advertiser has chosen not to accept applicants from your region.
9