Clinical Research Associate

We are a San Diego based biotechnology company focused in the oncology space. We are looking for a junior CRA to join the team. Please contact me for more details!

Opportunity for growth
100% benefits paid for
Quarterly team meetings
Robust portfolio of assets targeting cancer

We are seeking a highly motivated and experienced Clinical Research Associate to join our team. The successful candidate will have a minimum of 2 years of experience as a CRA or in an academic research setting. The role will focus on oncology and solid tumors, with an emphasis on clinical trials and regulatory guidelines. The position is full-time and offers competitive compensation and benefits packages. This role requires direct experience as an Oncology CRA in the pharmaceutical, biotech, or CRO space!!

Responsibilities:

• Conduct clinical monitoring activities at investigational sites to ensure compliance with study protocols, regulatory guidelines, and SOPs.
• Perform site qualification, initiation, and close-out visits, including site selection, site initiation, and site closure.
• Collaborate with cross-functional teams to ensure the successful execution of clinical trials, including data management, biostatistics, and medical writing.
• Maintain accurate and up-to-date study documentation, including monitoring reports, site visit reports, and study-related correspondence.
• Ensure timely and accurate data collection and entry into the electronic data capture system.
• Identify and escalate study issues to the appropriate stakeholders, including the clinical project manager, medical monitor, and regulatory affairs.
• Ensure the safety and welfare of study participants by monitoring adverse events and serious adverse events.

Qualifications:

• Bachelor's degree in life sciences or related field.
• Minimum of 2 years of experience as a CRA in the biotechnology or pharmaceutical industry or academic space
• Experience in oncology and solid tumors is required.
• Knowledge of clinical trial design, conduct, and analysis.
• Familiarity with regulatory guidelines and SOPs.
• Excellent communication and interpersonal skills.
• Ability to work independently and collaboratively in a team environment.
• Strong organizational and time-management skills.
• Ability to travel up to 50% of the time.

Join our team and make a difference in the lives of patients with cancer. We are committed to developing innovative therapies that improve patient outcomes and advance the field of oncology. If you are passionate about clinical research and have the necessary experience, we encourage you to apply.