Oncology CRA-Sponsor side!

Jobot; Washington (District of Columbia); Remote; USD 125,000 - 140,000; Full time

Job summary

Jobot is seeking 1 Clinical Research Associate to join a small, clinical-stage biotech focused on cancer. This is a full-time position with remote or hybrid work and a salary of $125,000 to $140,000 per year.

The successful candidate will have 3–5 years of Oncology CRA experience, knowledge of FDA regulations, and hands-on trial management using CTMS. You will oversee site visits, ensure protocol compliance, and collaborate across investigators to advance innovative cancer therapies.

Qualifications

• Bachelor's degree in life science or related field required
• 3–5 years Oncology CRA experience in biotech/pharma
• Experience managing/co-managing clinical trials across phases
• Strong knowledge of FDA regulations and guidelines
• Excellent organizational and communication skills
• Proficient in using CTMS and related software
• Experience with solid tumors is a must

Responsibilities

• Oversee design, implementation, and management of clinical trials from inception to completion
• Ensure sites comply with protocol, FDA regs, and regulatory requirements
• Conduct site visits to monitor progress, verify data, and resolve issues
• Collaborate with investigators and staff to protect participant safety and rights
• Prepare and review study documents such as protocols and CRFs
• Coordinate with data management to ensure data accuracy
• Prepare and present trial results to internal teams and regulators

Skills

Oncology CRA experience

Clinical trial management

FDA regulatory knowledge

Site oversight

strong communication

Education

Bachelor's degree in life science or related field

Tools

CTMS

Job description

Remote Oncology CRA position!

Job details

Salary: $125,000 - $140,000 per year

We are a small, clinical stage biotech focused on developing novel medicines for cancer. We are hiring 1 CRA on a remote or hybrid basis, with strong experience in Oncology.

Why join us?

• Financially stable, late phase biotech company
• Strong pipeline
• Opportunity for growth
• Flexible Schedule

Job Details

We are seeking 1 Clinical Research Associate's (CRA) to join our biotech startup. This is a full-time position that offer the opportunity to work on groundbreaking clinical research projects. The successful candidate 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

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

1. A bachelor's degree in a life science, nursing, or a related field. An advanced degree is preferred.
2. A minimum of 3-5 years of Oncology experience as a Clinical Research Associate in the biotech/pharma space.
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!

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. It is Jobot’s policy to comply with all applicable federal, state and local laws respecting consideration of unemployment status in making hiring decisions.

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.