Oncology Clinical Research Associate; CRA
Listed on 2026-01-14
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Healthcare
Clinical Research
Oncology Clinical Research Associate (CRA)
Base pay range: $/yr - $/yr
We are a small, clinical stage biotech focused on developing novel medicines for cancer. We are hiring 2 CRA's on a remote or hybrid basis, with strong experience in Oncology. Please apply if you fit the requirements below.
Benefits- Financially stable, late phase biotech company
- Strong pipeline
- Opportunity for growth
- Flexible Schedule
- Assisting with the oversight of the design, implementation, and management of clinical trials from inception to completion.
- Ensuring the clinical sites are compliant with the study protocol, FDA regulations, and other applicable regulatory requirements.
- Conducting site visits to assess the progress of the trials, verify data accuracy, and resolve any issues that may arise.
- Collaborating with investigators and other clinical staff to ensure the safety and rights of the participants are protected.
- Preparing and reviewing study-related documents such as protocols, informed consent forms, and case report forms.
- Coordinating with the data management team to ensure the data collected is accurate and reliable.
- Participating in the preparation and presentation of clinical trial results to internal teams, regulatory agencies, and other stakeholders.
- A bachelor's degree in a life science, nursing, or a related field. An advanced degree is preferred.
- Minimum of 2 years of Oncology experience as a Clinical Research Associate or a similar role in the scientific industry.
- Proven experience in managing/co-managing clinical trials, including experience with different phases of clinical research.
- Thorough understanding of FDA regulations and guidelines related to clinical research.
- Strong organizational skills with the ability to manage multiple tasks and meet deadlines.
- Excellent communication and interpersonal skills, with the ability to interact effectively with a diverse team of professionals.
- Proficient in using clinical trial management systems and other related software.
- Experience with solid tumors is a must.
Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories.
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We encourage you to apply and contribute to the advancement of medical science and improve patient outcomes.
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