CRA (Oncology) Sponsor side!

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

About the role

This is a full-time position that offers the opportunity to work on groundbreaking clinical research projects. The successful candidate will collaborate with a team of highly skilled professionals and contribute to the development of innovative medical treatments and therapies.

Responsibilities

• Assist with the oversight of the design, implementation, and management of clinical trials from inception to completion.
• Ensure clinical sites are compliant with the study protocol, FDA regulations, and other applicable regulatory requirements.
• Conduct site visits to assess the progress of the trials, verify data accuracy, and resolve any issues that may arise.
• Collaborate with investigators and other clinical staff to ensure the safety and rights of participants are protected.
• Prepare and review study-related documents such as protocols, informed consent forms, and case report forms.
• Coordinate with the data management team to ensure the data collected is accurate and reliable.
• Participate 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 or 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.
• Proficiency in using clinical trial management systems and other related software.
• Experience with solid tumors is required.

Pay

$125,000 - $140,000 per year

Benefits

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