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Title
Text copied to clipboard!Clinical Research Oncologist
Description
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We are looking for a Clinical Research Oncologist to join our dynamic team in the fight against cancer. This role involves conducting and overseeing clinical trials to discover more effective treatments and therapies for cancer patients. The ideal candidate will have a strong background in oncology and clinical research, with a passion for advancing medical knowledge and improving patient outcomes. You will work closely with a team of researchers, doctors, and healthcare professionals to design, implement, and analyze clinical studies. Your work will contribute to the development of new cancer treatments, making a significant impact on the lives of patients around the world. This position requires a deep understanding of oncology, excellent analytical skills, and the ability to work collaboratively in a fast-paced, multidisciplinary environment. You will be responsible for ensuring that all research activities comply with regulatory standards and ethical guidelines. If you are committed to advancing the field of oncology through research and have a track record of success in clinical trials, we encourage you to apply.
Responsibilities
Text copied to clipboard!- Design and implement clinical trials to test new cancer treatments.
- Monitor patient health and response to treatments throughout the trial.
- Analyze data from clinical trials to determine effectiveness and safety of treatments.
- Collaborate with multidisciplinary teams to ensure trials are conducted efficiently.
- Prepare and submit research findings to medical journals and conferences.
- Stay up-to-date with advancements in oncology and clinical research methodologies.
- Ensure all research activities comply with regulatory standards and ethical guidelines.
- Develop protocols and case report forms for clinical trials.
- Provide mentorship and guidance to junior researchers and staff.
- Communicate with stakeholders, including patients, healthcare professionals, and pharmaceutical companies.
- Review and interpret medical literature to inform trial designs.
- Manage the budget and resources for clinical research projects.
- Obtain informed consent from trial participants.
- Report adverse events and manage patient safety issues.
- Coordinate with regulatory bodies for trial approvals and compliance.
- Lead patient recruitment efforts for clinical trials.
- Evaluate and select appropriate biomarkers for trials.
- Assist in grant writing and funding applications for research projects.
Requirements
Text copied to clipboard!- MD or DO degree with specialization in oncology.
- Board certification in oncology.
- Experience in conducting clinical research and trials.
- Strong understanding of GCP, ICH guidelines, and regulatory requirements.
- Excellent analytical and problem-solving skills.
- Ability to work collaboratively in a multidisciplinary team.
- Strong communication and interpersonal skills.
- Proficiency in statistical software and data analysis.
- Commitment to ethical research practices.
- Ability to manage multiple projects and meet deadlines.
- Experience in writing research proposals and publications.
- Familiarity with electronic data capture systems.
- Leadership skills and experience in mentoring junior staff.
- Willingness to stay up-to-date with the latest research and treatment advancements.
- Flexibility to adapt to changing research priorities.
- Experience in patient recruitment and consent processes.
- Knowledge of biomarker selection and evaluation.
- Ability to secure funding for research projects.
Potential interview questions
Text copied to clipboard!- Can you describe your experience with clinical trial design and implementation?
- How do you stay informed about the latest advancements in oncology research?
- What strategies do you use to ensure compliance with regulatory standards in your research?
- Can you provide an example of a challenging clinical trial you managed and how you overcame the challenges?
- How do you approach patient recruitment and informed consent processes?
- What is your experience with data analysis and statistical software in clinical research?
- How do you handle adverse events during a clinical trial?
- Can you discuss a research project you led that had a significant impact on patient care?
- How do you manage the budget and resources for a research project?
- What is your approach to mentoring junior researchers and staff?