10,266 Oncology Research jobs in the United States

**Job Description**
Saint Luke's is looking for an **Experienced Nurse** to join their **Research Team** specific to **Neuro Oncology** .
Schedule: Monday - Friday, 8 am to 5 pm
The Clinical Research Nurse has multiple responsibilities related to clinical research studies. These responsibilities may vary according to study protocol and the primary activities include assisting in the evaluation of new protocols for feasibility at the site preparing the site for conduct of the study such as establishing study files and training study related staff disseminating study information to physicians and ancillary departments preparing the Institutional Review Board submissions performing informed consent process with potential subjects coordinating study conduct throughout the trial screening and recruiting subjects gathering and recording study related data according to protocol overseeing drug device accountability maintaining regular communications with sponsors or CROs and IRBs collaborating with other SLH departments providing study services.
**Job Requirements**
Applicable Experience:
Less than 1 year
Registered Nurse (KS) - National Council of State Boards of Nursing (NURSYS), Registered Nurse (MO) - National Council of State Boards of Nursing (NURSYS)
Associate Degree
**Job Details**
Full Time
Day (United States of America)
**_The best place to get care. The best place to give care_** **. Saint Luke's 12,000 employees strive toward that vision every day. Our employees are proud to work for the only faith-based, nonprofit, locally owned health system in Kansas City. Joining Saint Luke's means joining a team of exceptional professionals who strive for excellence in patient care. Do the best work of your career within a highly diverse and inclusive workspace where all voices matter.**
**Join the Kansas City region's premiere provider of health services. Equal Opportunity Employer.**

**Join Amgen's Mission of Serving Patients**
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
**Scientist - Oncology Research**
**What you will do**
Let's do this. Let's change the world. . The Oncology research group at Amgen is searching for a highly motivated Scientist to join our dynamic and supportive team. In this vital role, you will contribute to the discovery and validation of oncology targets and therapeutic strategies and support the advancement of pipeline projects by generating and communicating decision-enabling data packages.
**Key Responsibilities:**
+ Design and perform in vitro studies to assess the biology of novel targets and evaluate mechanisms of action of therapeutic molecules
+ Collaborate closely with colleagues to support the execution of pharmacodynamic studies
+ Perform literature and database surveys to support new target ideation and validation
+ Operation and maintenance of laboratory equipment, accurate, timely record-keeping, and data analysis
+ Consistent delivery of high-quality, actionable data
+ Effective communication of plans, results, and analyses to cross-functional teams
**What we expect of you**
We are all different, yet we all use our unique contributions to serve patients. The committed and creative professional we seek is a team player with these qualifications.
**Basic Qualifications:**
Doctorate degree
**Or**
Master's degree and 2 years of Scientific experience
**Or**
Bachelor's degree and 4 years of Scientific experience
**Preferred Qualifications:**
+ Master's Degree in immunology or cell biology, or a related subject area, and 3+ years of scientific experience in an industry setting or recently graduated Ph.D
+ Extensive experience with a broad range of molecular and cell biology techniques, e.g. cell culture, flow cytometry, western blotting, genome editing.
+ Prior experience with assays used to evaluate T-cell engager and / or antibody-drug conjugates is preferred
+ Demonstrated track record of independent critical thinking and scientific achievement as exemplified by your publication record and / or significant contribution to a therapeutic program
+ Proactive, curious, and eager to learn and grow
**What you can expect of us**
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
+ A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
+ A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
+ Stock-based long-term incentives
+ Award-winning time-off plans
+ Flexible work models, including remote and hybrid work arrangements, where possible
**Apply now and make a lasting impact with the Amgen team.**
**careers.amgen.com**
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
**Application deadline**
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Our client, a leading pharmaceutical innovator, is seeking a highly skilled and motivated Clinical Research Scientist to join their oncology drug development team in Phoenix, Arizona . This role is essential for driving forward critical research initiatives aimed at developing groundbreaking treatments for cancer. The successful candidate will be instrumental in the design, execution, and interpretation of clinical trials, working closely with internal and external stakeholders. Responsibilities include developing clinical trial protocols, managing study sites, ensuring adherence to regulatory requirements (FDA, EMA, etc.), analyzing and reporting clinical data, and contributing to scientific publications and presentations. You will also be responsible for staying abreast of the latest scientific advancements in oncology, identifying potential new drug targets, and collaborating with preclinical research teams to ensure seamless transition of compounds into clinical development. The ideal candidate will hold a Ph.D. or M.D. in a relevant scientific field (e.g., oncology, pharmacology, molecular biology) with at least 5 years of experience in clinical trial design and management within the pharmaceutical or biotech industry. Demonstrated expertise in oncology research and a deep understanding of the drug development process are mandatory. Excellent analytical, problem-solving, and communication skills are required, along with the ability to lead cross-functional teams and manage multiple projects simultaneously. A strong publication record and experience with statistical analysis of clinical data are highly desirable. This is an exceptional opportunity to make a significant impact on patient lives by contributing to the development of life-saving therapies in a collaborative and scientifically rigorous environment.

Our client, a leading pharmaceutical company, is seeking a dedicated and highly qualified Clinical Research Scientist specializing in Oncology to join their innovative team in Las Vegas, Nevada, US . This critical role will focus on the design, execution, and analysis of clinical trials for novel cancer therapies. The ideal candidate will possess a strong scientific background in oncology and drug development, coupled with extensive experience in clinical trial management. You will be responsible for developing clinical protocols, identifying and assessing potential study sites, and overseeing the conduct of clinical trials to ensure patient safety and data integrity. Key responsibilities include collaborating with investigators, clinicians, and regulatory authorities, analyzing clinical data, and contributing to the interpretation of study results. You will also play a key role in preparing regulatory submissions and scientific publications. The ideal candidate will have a PhD or MD in a relevant scientific discipline, with a proven track record in oncology research. Strong understanding of Good Clinical Practice (GCP) guidelines, regulatory requirements, and biostatistics is essential. Excellent written and verbal communication skills, as well as strong leadership and team collaboration abilities, are required. We are looking for a highly motivated individual with a passion for advancing cancer treatment and a commitment to scientific excellence. This is a significant opportunity to contribute to groundbreaking research and make a tangible impact on patient lives within a dynamic pharmaceutical environment. Experience in early-phase oncology trials is a plus.

Our client has an exciting opportunity for a Clinical Research Scientist specializing in Oncology to be based in Baltimore, Maryland, US . This role is pivotal in designing, implementing, and managing clinical trials that advance our understanding and treatment of cancer. The successful candidate will be responsible for the scientific integrity of clinical studies, ensuring compliance with all regulatory requirements and ethical guidelines. You will contribute to the development of clinical trial protocols, oversee data collection and analysis, and interpret study results. This position requires a strong scientific background in oncology and a comprehensive understanding of clinical trial methodologies.

Key responsibilities include collaborating with investigators, site staff, and regulatory agencies to ensure smooth trial execution. You will also be involved in preparing scientific publications, presentations, and regulatory submissions. The role involves staying abreast of the latest scientific advancements and clinical research trends in oncology. A key aspect of this position is to identify opportunities for innovation and improvement in clinical trial design and execution. You will work closely with internal R&D teams, as well as external partners and key opinion leaders in the field. The ability to critically evaluate scientific literature and translate complex data into clear, concise reports is essential. We are seeking a highly analytical and detail-oriented scientist with excellent communication and leadership skills. This is a challenging yet rewarding role for someone passionate about making a difference in cancer patient care.

Qualifications: Ph.D. or M.D. in a relevant scientific field (e.g., Biology, Pharmacology, Medicine) with a specialization in Oncology. Minimum of 5 years of experience in clinical research, preferably within the pharmaceutical industry or academia. Strong understanding of drug development processes and regulatory requirements (e.g., FDA, EMA). Proven experience in designing and managing oncology clinical trials (Phase I-IV). Excellent scientific writing and presentation skills. Ability to work independently and collaboratively in a fast-paced environment. Strong project management skills and attention to detail. Must be eligible to work in the US. This is a critical role in advancing cancer therapies.

Our client is a pioneering pharmaceutical company seeking a dedicated Clinical Research Scientist specializing in Oncology to join their esteemed research division in **Kansas City, Missouri, US**. This critical role involves leading and contributing to the design, execution, and interpretation of clinical trials for novel cancer therapies. The Clinical Research Scientist will work at the forefront of oncological drug development, translating scientific hypotheses into actionable clinical research plans. Responsibilities include developing clinical protocols, identifying suitable trial sites and investigators, overseeing study conduct, and ensuring compliance with regulatory guidelines (e.g., FDA, EMA). You will analyze clinical data, collaborate with biostatisticians and data managers, and author clinical study reports and regulatory submissions. A deep understanding of cancer biology, drug development processes, and clinical trial methodologies is essential. The ability to interpret complex scientific and clinical data, identify potential risks, and propose solutions is paramount. We are seeking an individual with strong scientific acumen, excellent project management skills, and a passion for advancing cancer treatment. This hybrid role offers a balance of in-office collaboration and remote flexibility, allowing you to contribute effectively to our groundbreaking work.

Responsibilities:

• Design and develop clinical trial protocols for oncology therapeutics.
• Oversee the execution of clinical trials, ensuring adherence to protocols and regulatory standards.
• Identify and assess potential clinical trial sites and investigators.
• Collaborate with cross-functional teams including regulatory affairs, biostatistics, and data management.
• Analyze and interpret clinical trial data, contributing to study conclusions.
• Author clinical study reports, manuscripts, and regulatory submission documents.
• Stay abreast of scientific advancements and emerging trends in oncology drug development.
• Ensure compliance with Good Clinical Practice (GCP) and other relevant guidelines.
• Provide scientific expertise and support to internal and external stakeholders.
• Contribute to the strategic planning of the oncology pipeline.

Qualifications:

• M.D., Ph.D., or Pharm.D. with a strong background in oncology or a related life science field.
• Minimum of 5 years of experience in clinical research, preferably within the pharmaceutical industry.
• Proven experience in designing and managing oncology clinical trials.
• In-depth knowledge of cancer biology, therapeutic strategies, and drug development processes.
• Familiarity with regulatory requirements (FDA, EMA) for clinical trials.
• Excellent scientific and critical thinking skills.
• Strong project management and organizational abilities.
• Effective communication and interpersonal skills.

A globally recognized pharmaceutical company is seeking a highly motivated and experienced Clinical Research Scientist specializing in Oncology to be based in or near Durham, North Carolina, US . This critical role will contribute to the design, execution, and interpretation of clinical trials aimed at developing novel cancer therapies. You will be at the forefront of scientific innovation, working collaboratively with cross-functional teams including medical affairs, regulatory affairs, biostatistics, and clinical operations. Responsibilities include contributing to the development of clinical trial protocols, ensuring scientific rigor and adherence to regulatory guidelines; analyzing and interpreting complex clinical data; preparing scientific reports, manuscripts, and presentations for internal and external dissemination; staying abreast of the latest scientific advancements and competitive landscape in oncology; providing scientific input for regulatory submissions; and engaging with key opinion leaders in the field. The ideal candidate will hold a Ph.D. or M.D. with a strong background in oncology or a related biomedical science, coupled with at least 5 years of experience in clinical research within the pharmaceutical industry or an academic setting focused on drug development. A deep understanding of clinical trial design, statistical principles, and regulatory requirements (e.g., FDA, EMA) is essential. Exceptional written and oral communication skills, along with strong analytical and problem-solving abilities, are paramount. Experience with specific oncology therapeutic areas such as breast cancer, lung cancer, or hematologic malignancies is highly desirable. This is an exceptional opportunity to join a leading organization dedicated to improving patient outcomes through groundbreaking research and development. Be part of a dynamic team that values scientific excellence, collaboration, and innovation in the fight against cancer. This role offers a competitive salary and benefits package, along with opportunities for professional growth and development in a stimulating research environment. Extensive experience in planning and managing Phase II and Phase III oncology trials is expected.

Our client, a forward-thinking pharmaceutical company at the forefront of innovative therapies, is seeking a highly skilled Clinical Research Scientist specializing in Oncology. This critical role, based in Detroit, Michigan, US , will contribute significantly to the advancement of novel cancer treatments. You will be instrumental in the design, execution, and interpretation of clinical trials, from Phase I through late-stage development. Responsibilities include developing clinical trial protocols, identifying and evaluating investigational sites, and overseeing the ethical and scientific conduct of studies. You will analyze trial data, generate comprehensive reports, and present findings to internal teams, regulatory bodies, and scientific conferences. Close collaboration with cross-functional teams, including R&D, regulatory affairs, and medical affairs, is essential. The ideal candidate will possess a Ph.D. or M.D. with a specialization in oncology or a related biomedical science. Proven experience in clinical trial design and management within the pharmaceutical industry is required. You must have a strong understanding of regulatory guidelines (FDA, EMA) and Good Clinical Practice (GCP). Exceptional analytical, problem-solving, and scientific writing skills are paramount. This hybrid role requires a commitment to in-office collaboration for key meetings and lab work while offering remote flexibility for data analysis and report writing. If you are a driven scientist passionate about making a difference in the lives of cancer patients through cutting-edge research, we encourage you to apply.

Our client, a leading pharmaceutical company, is seeking a highly motivated and experienced Clinical Research Scientist specializing in Oncology. This is a fully remote position, offering the flexibility to work from home across the US. You will play a crucial role in the design, execution, and interpretation of clinical trials for novel cancer therapies. The ideal candidate will possess a strong scientific background, extensive knowledge of oncology drug development, and a proven track record in clinical research. Responsibilities include contributing to clinical trial protocols, developing statistical analysis plans, overseeing data collection and analysis, and preparing scientific reports and publications. You will collaborate closely with cross-functional teams, including R&D, regulatory affairs, and medical affairs, to ensure the successful advancement of clinical programs. A deep understanding of regulatory requirements (e.g., FDA, EMA) and good clinical practice (GCP) is essential. The successful candidate will have excellent analytical, problem-solving, and critical thinking skills, as well as strong written and verbal communication abilities. Experience with clinical trial design and management, statistical software, and data visualization tools is highly desirable. We are looking for a passionate and dedicated scientist who is committed to advancing cancer research and improving patient outcomes. This is an exceptional opportunity to make a significant contribution to life-saving therapies within a leading pharmaceutical organization, with the convenience of a remote work arrangement.