7,749 Oncology Research jobs in the United States

• Contribute to the design and development of clinical trial protocols for oncology indications.
• Oversee and manage various aspects of clinical trial execution, ensuring adherence to protocols and regulatory guidelines (ICH GCP, FDA).
• Analyze and interpret clinical trial data, collaborating with statisticians and data management teams.
• Prepare clinical study reports, regulatory submissions (e.g., IND, NDA), and scientific publications.
• Provide scientific and clinical expertise to internal teams, including regulatory affairs, medical affairs, and R&D.
• Collaborate with external investigators, study sites, and key opinion leaders (KOLs) in oncology.
• Monitor trial progress, identify potential risks or issues, and implement mitigation strategies.
• Ensure the quality and integrity of clinical data collected throughout the study lifecycle.
• Stay abreast of the latest advancements in oncology research, therapeutic strategies, and clinical trial methodologies.
• Participate in the selection and evaluation of potential drug candidates for clinical development.

• Ph.D. or M.D. in a relevant life science field (e.g., Biology, Pharmacology, Medicine).
• Minimum of 5 years of experience in clinical research, with a significant focus on oncology drug development.
• Thorough understanding of clinical trial design, conduct, and data analysis.
• Knowledge of regulatory requirements for drug development (FDA, EMA).
• Experience with scientific writing, protocol development, and regulatory submissions.
• Strong analytical and critical thinking skills.
• Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse teams.
• Proficiency in Microsoft Office Suite and clinical data management systems.

• Develop and execute clinical trial protocols.
• Oversee clinical site selection and performance.
• Ensure compliance with GCP and regulatory guidelines.
• Analyze and interpret clinical trial data.
• Collaborate with cross-functional teams and external stakeholders.
• Manage pharmacovigilance activities.
• Prepare regulatory submissions and reports.
• Contribute to strategic planning for clinical development.

• Designing clinical trial protocols, including study objectives, endpoints, patient population, and statistical considerations.
• Overseeing the operational aspects of clinical trials, ensuring adherence to protocol, GCP, and regulatory requirements.
• Collaborating with investigators and site staff to facilitate trial recruitment and patient management.
• Analyzing clinical data, interpreting results, and contributing to scientific publications and presentations.
• Developing and maintaining relationships with key opinion leaders (KOLs) in the field of oncology.
• Preparing regulatory submissions and responding to inquiries from health authorities.
• Monitoring study progress, identifying potential risks, and implementing mitigation strategies.
• Contributing to the development of new drug candidates and therapeutic strategies.
• Staying abreast of the latest advancements in oncology and clinical research methodologies.
• Ensuring the quality and integrity of clinical trial data.

• Advanced degree (Ph.D. or M.D.) in a life science, medical, or related field.
• Minimum of 5 years of experience in clinical research, with a significant focus on oncology trials.
• In-depth knowledge of cancer biology, pharmacology, and treatment paradigms.
• Strong understanding of ICH-GCP guidelines and regulatory requirements for clinical trials.
• Excellent analytical, statistical, and problem-solving skills.
• Proficiency in clinical data management systems and statistical software.
• Exceptional written and verbal communication skills, with the ability to present complex data clearly.
• Demonstrated ability to manage multiple projects simultaneously and meet tight deadlines.
• Experience in protocol development and writing.
• Ability to work effectively in a collaborative, fast-paced environment.

• Contribute to the development and refinement of clinical trial protocols for oncology studies.
• Provide scientific and clinical input throughout the study lifecycle, from planning to analysis and reporting.
• Monitor study progress, ensuring data quality, protocol compliance, and patient safety.
• Analyze and interpret clinical trial data, contributing to study reports and scientific publications.
• Collaborate with cross-functional teams to ensure effective study execution.
• Liaise with investigators, site personnel, and key opinion leaders.
• Prepare clinical sections of regulatory submission documents (e.g., IND, NDA).
• Stay abreast of the latest scientific advancements and therapeutic strategies in oncology.
• Contribute to the overall clinical development strategy for pipeline assets.
• Ensure compliance with all applicable regulatory requirements and company policies.

• Ph.D. or M.D. in a relevant life science discipline (e.g., Biology, Pharmacology, Medicine).
• Minimum of 5 years of experience in clinical research, with a significant focus on oncology drug development.
• In-depth knowledge of clinical trial design, conduct, and data analysis.
• Familiarity with ICH-GCP guidelines and regulatory submission processes.
• Strong scientific writing and communication skills.
• Ability to work independently and collaboratively in a team environment.
• Excellent project management and organizational skills.
• Experience with statistical analysis is a plus.

Its More Than a Career, Its a Mission.

Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.

Our Mission

People who live with cancer those who work to prevent it, fight it, and survive it are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.

As an Enrollment Research Nurse your prim ary responsibility is to screen and enroll oncology research study subjects e nsuring protocol compliance. You will enroll patients onto clinical trials through recruitment, s creening, enrollment and follow- up of eligible subjects.

• You will be familiar with the protocols on which the patients are enrolled, screen and treat.

• You will review the study design and inclusion/exclusion criteria with physician and patient.

• You will complete and document screening/eligibility and consent accurately and have all parties fully execute the document including HIPAA Authorization.

• You will complete the inclusion/exclusion form and standard enrollment form accurately and assess the patient and document findings at each clinic visit while on protocol.

• You will document all specific tools required by the protocol ( i.e. oral medication forms, pill count diaries, quality of life questionnaires, neuro exams, vital signs sheets, times of PK draws, etc.).

• You will screen every new patient or patient returning to office with scan results and document appropriately on the patient tracking logs.

• You will complete the study medication order form and have the physician or nurse practitioner sign orders prior to treatment and ensure that all medications, including antiemetics , are approved by the registrar prior to initiating treatment or when changing medication regimens, such as crossover studies

• You will accurately calculate and the BSA, creatinine clearance, urine protein:creatinine ratio or any other conversions needed per protocol.

• You will obtain completed and signed waivers prior to submitting forms to enrollment coordinator for investigator-initiated protocols and re-consent patients in a timely manner and document process appropriately.

What you should have for this role:

• Associate of Nursing Degree; Bachelor of Nursing is preferred.

• Nursing license for the State of Tennessee

• Knowledge of medical and oncology research terminology and of federal regulations, good clinical practices (GCP).

• One year of clinical nursing experience

• One year of clinical research experience is preferred

• One year of experience treating oncology patients is preferred

About Sarah Cannon Research Institute

Sarah Cannon Research Institute (SCRI) is one of the worlds leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 750 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA today. SCRIs research network brings together more than 1,300 physicians who are actively enrolling patients into clinical trials at more than 250 locations in 24 states across the U.S. Please click here to learn more about our research offerings.

We care about the well-being of the patients and communities we serve, and that starts with caring for our people. Thats why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please click here .

As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.