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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 oncology research team. This role involves designing, conducting, and overseeing clinical trials focused on cancer treatments and therapies. The ideal candidate will have a strong background in oncology, clinical research methodologies, and patient care. You will collaborate with multidisciplinary teams including physicians, research coordinators, data managers, and pharmaceutical sponsors to ensure the successful execution of clinical trials.
As a Clinical Research Oncologist, you will be responsible for identifying eligible patients, obtaining informed consent, administering investigational treatments, and monitoring patient outcomes. You will also be expected to analyze data, contribute to scientific publications, and present findings at medical conferences. Your work will directly contribute to the advancement of cancer treatment and patient care.
This position requires a deep understanding of regulatory requirements, Good Clinical Practice (GCP), and ethical considerations in human subject research. You must be comfortable working in a fast-paced environment and managing multiple clinical trials simultaneously. Strong communication skills, attention to detail, and a commitment to patient safety are essential.
We offer a collaborative work environment, opportunities for professional development, and the chance to make a meaningful impact in the field of oncology. If you are passionate about cancer research and improving patient outcomes, we encourage you to apply.
Responsibilities
Text copied to clipboard!- Design and implement oncology clinical trials
- Recruit and screen eligible patients for studies
- Obtain informed consent and ensure ethical compliance
- Administer investigational treatments and monitor patient responses
- Collaborate with multidisciplinary research teams
- Maintain accurate and timely documentation of trial activities
- Analyze clinical data and contribute to publications
- Ensure compliance with regulatory and institutional guidelines
- Present research findings at conferences and meetings
- Participate in protocol development and review processes
Requirements
Text copied to clipboard!- Medical degree (MD or DO) with specialization in oncology
- Board certification in oncology preferred
- Experience in clinical research and trial management
- Knowledge of GCP and regulatory requirements
- Strong analytical and problem-solving skills
- Excellent communication and interpersonal abilities
- Ability to manage multiple projects simultaneously
- Commitment to ethical research practices
- Proficiency in data analysis and medical software
- Willingness to travel for conferences and site visits
Potential interview questions
Text copied to clipboard!- Do you have board certification in oncology?
- How many years of clinical research experience do you have?
- Have you led or participated in oncology clinical trials?
- Are you familiar with GCP and FDA regulations?
- Can you describe your experience with patient recruitment?
- What data analysis tools have you used in research?
- How do you ensure ethical compliance in clinical trials?
- Are you comfortable presenting research findings publicly?
- Do you have experience working with multidisciplinary teams?
- Are you willing to travel for research-related activities?
