Oncology CRA-Sponsor side!

Jobot; Rockville (MD); Hybrid; USD 125,000 - 140,000; Full time

Benefits offered by this job

Flexible Schedule

Remote/Hybrid Work Option

Job summary

Jobot is seeking a Clinical Research Associate (CRA) with strong Oncology experience for a remote or hybrid role. This full-time position offers $125,000–$140,000 per year and the chance to contribute to cutting-edge cancer research within a stable biotech environment.

The ideal candidate holds a life science degree, 3–5 years of Oncology CRA experience, and deep knowledge of FDA regulations. You will oversee trials, ensure site compliance, and collaborate across teams to protect participant

Qualifications

• Bachelor's degree in life science or related field; advanced degree preferred.
• 3–5 years Oncology experience as CRA in biotech/pharma.
• Experience managing/co-managing clinical trials across phases.
• Strong knowledge of FDA regulations and guidelines for clinical research.
• Excellent communication, organization, and problem-solving skills.
• Experience with solid tumors is required.

Responsibilities

• Oversee design, implementation, and management of clinical trials from inception to completion.
• Ensure sites comply with protocol, FDA regulations, 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 informed consent forms.
• Coordinate with data management to ensure accurate, reliable data.
• Assist in presenting trial results to internal teams and regulators.

Skills

Oncology experience

Clinical trial management

FDA regulations knowledge

Communication skills

Organizational skills

Education

Bachelor's degree in life sciences

Advanced degree preferred

Tools

CTMS

Data management software

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.

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