Sr. CRA (Oncology)
- $125,000 - $140,000
- Rockville, MD
Remote Oncology Sr. CRA position!
A bit about us:
We are a small, clinical stage biotech focused on developing novel medicines for cancer. We are hiring 2 Sr. CRA's on a remote or hybrid basis, with strong experience in Oncology. Please apply if you fit the requirements below!
Why join us?
Financially stable, late phase biotech company
Strong pipeline
Opportunity for growth
Flexible Schedule
Strong pipeline
Opportunity for growth
Flexible Schedule
Job Details
Job Details:
We are seeking 2 Clinical Research Associate's (CRA) to join our biotech startup. These are full-time positions that offers the opportunity to work on groundbreaking clinical research projects. The successful candidates will have the chance to collaborate with a team of highly skilled professionals and contribute to the development of innovative medical treatments and therapies.
Responsibilities:
The Clinical Research Associate's will be responsible for a broad range of tasks, including but not limited to:
1. Assisting with the oversight of the design, implementation, and management of clinical trials from inception to completion.
2. Ensuring the clinical sites are compliant with the study protocol, FDA regulations, and other applicable regulatory requirements.
3. Conducting site visits to assess the progress of the trials, verify data accuracy, and resolve any issues that may arise.
4. Collaborating with investigators and other clinical staff to ensure the safety and rights of the participants are protected.
5. Preparing and reviewing study-related documents such as protocols, informed consent forms, and case report forms.
6. Coordinating with the data management team to ensure the data collected is accurate and reliable.
7. Participating in the preparation and presentation of clinical trial results to internal teams, regulatory agencies, and other stakeholders.
Qualifications:
To be considered for this exciting opportunity, candidates must possess the following qualifications:
1. A bachelor's degree in a life science, nursing, or a related field. An advanced degree is preferred.
2. A minimum of 2 years of Oncology experience as a Clinical Research Associate or a similar role in the scientific industry.
3. Proven experience in managing/co-managing clinical trials, including experience with different phases of clinical research.
4. A thorough understanding of FDA regulations and guidelines related to clinical research.
5. Strong organizational skills with the ability to manage multiple tasks and meet deadlines.
6. Excellent communication and interpersonal skills, with the ability to interact effectively with a diverse team of professionals.
7. Proficient in using clinical trial management systems and other related software.
8. Experience with solid tumors is a must.
This position offers a unique opportunity to contribute to the advancement of medical science and improve patient outcomes. If you are a motivated professional with a passion for clinical research, we encourage you to apply!
We are seeking 2 Clinical Research Associate's (CRA) to join our biotech startup. These are full-time positions that offers the opportunity to work on groundbreaking clinical research projects. The successful candidates will have the chance to collaborate with a team of highly skilled professionals and contribute to the development of innovative medical treatments and therapies.
Responsibilities:
The Clinical Research Associate's will be responsible for a broad range of tasks, including but not limited to:
1. Assisting with the oversight of the design, implementation, and management of clinical trials from inception to completion.
2. Ensuring the clinical sites are compliant with the study protocol, FDA regulations, and other applicable regulatory requirements.
3. Conducting site visits to assess the progress of the trials, verify data accuracy, and resolve any issues that may arise.
4. Collaborating with investigators and other clinical staff to ensure the safety and rights of the participants are protected.
5. Preparing and reviewing study-related documents such as protocols, informed consent forms, and case report forms.
6. Coordinating with the data management team to ensure the data collected is accurate and reliable.
7. Participating in the preparation and presentation of clinical trial results to internal teams, regulatory agencies, and other stakeholders.
Qualifications:
To be considered for this exciting opportunity, candidates must possess the following qualifications:
1. A bachelor's degree in a life science, nursing, or a related field. An advanced degree is preferred.
2. A minimum of 2 years of Oncology experience as a Clinical Research Associate or a similar role in the scientific industry.
3. Proven experience in managing/co-managing clinical trials, including experience with different phases of clinical research.
4. A thorough understanding of FDA regulations and guidelines related to clinical research.
5. Strong organizational skills with the ability to manage multiple tasks and meet deadlines.
6. Excellent communication and interpersonal skills, with the ability to interact effectively with a diverse team of professionals.
7. Proficient in using clinical trial management systems and other related software.
8. Experience with solid tumors is a must.
This position offers a unique opportunity to contribute to the advancement of medical science and improve patient outcomes. If you are a motivated professional with a passion for clinical research, we encourage you to apply!
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Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.
Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: jobot.com/privacy-policy