Oncology CRA-Sponsor side!

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

Benefits offered by this job

Flexible Schedule

Job summary

Jobot is hiring a Clinical Research Associate (Oncology) for a remote or hybrid role. The candidate will join a biotech startup to support cancer trials and regulatory compliance across multiple sites. A bachelor’s in a life science is required, with 3–5 years of Oncology CRA experience preferred.

This full-time role offers collaboration with a skilled team and opportunities to contribute to cutting-edge cancer therapies and meaningful clinical research outcomes.

Qualifications

• Bachelor's degree in life science, nursing, or related field; advanced degree preferred.
• 3–5 years Oncology experience as a CRA in biotech/pharma.
• Experience managing clinical trials and familiarity with FDA regulations.

Responsibilities

• Oversee design, implementation, and management of clinical trials from inception to completion.
• Ensure sites comply with study protocol and regulatory requirements.
• Conduct site visits to verify progress, data quality, and issue resolution.
• Collaborate with investigators to protect participant safety and rights.
• Prepare study documents and coordinate with data management for accuracy.
• Present trial results to internal teams and stakeholders.

Skills

Oncology experience

Clinical trial management

Regulatory compliance

Data management

Education

Bachelor's degree in life sciences

Advanced degree preferred

Tools

CTMS

Job description

Remote Oncology CRA position

Jobot Job is hosted by: Julian Okoro

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

A bit about us

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. Please apply if you fit the requirements below!

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

• 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.

Qualifications

• A bachelor's degree in a life science, nursing, or a related field. An advanced degree is preferred.
• A minimum of 3-5 years of Oncology experience as a Clinical Research Associate in the biotech/pharma space.
• Proven experience in managing/co-managing clinical trials, including experience with different phases of clinical research.
• A 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.

If you are a motivated professional with a passion for clinical research, we encourage you to apply!

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