RESPONSIBILITIES

• Adhere to Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements.
• Perform IV infusions of both blinded and unblinded investigational products in accordance with study protocols.
• Obtain blood specimens and other biological samples from study participants using proper clinical procedures.
• Ensure accurate, complete, and timely source documentation in compliance with GCP and sponsor guidelines.
• Monitor study participants for adverse events and report findings in accordance with study protocols and regulatory requirements.
• Maintain the confidentiality, security, and integrity of study data and participant information.
• Collaborate effectively with investigators, study coordinators, and other clinical staff to ensure protocol adherence.
• Participate in required training sessions and maintain current knowledge of clinical trial procedures, safety standards, and best practices.
• Represent the company in a professional and courteous manner in all interactions (verbal, written, and appearance) with staff, clients, and vendors.
• Perform additional duties as assigned by management.

QUALIFICATIONS

Education

• Registered Nurse (RN) with a current, active license.
• Nursing license must be in good standing.
• 1 year of Oncology experience.
• Proficient in Infusions.
• Good Clinical Practice (GCP) certification preferred.

Experience

• Minimum of 1–2 years of clinical research experience preferred.
• Proficiency in IV infusion and phlebotomy required.

Knowledge and Skills

• Strong knowledge of clinical research methods preferred.
• Exceptional attention to detail with a high level of accuracy in documentation.
• Demonstrated ability to collaborate effectively and align with operational teams.
• Excellent verbal and written communication skills.
• Strong computer proficiency, including Office 365 products.
• Experience reviewing and adhering to Standard Operating Procedures (SOPs) preferred.
• Strong problem-solving skills, including risk assessment and impact analysis.
• Demonstrated experience with process improvement initiatives.
• Flexible and adaptable, with the ability to multitask and prioritize competing demands.
• Ability to think independently and influence decisions when appropriate.

The company offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others!

^*We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO), and the California Fair Chance Act (CFCA).

^*As a job position within our Clinical Sciences division, a successful completion of a background check may be required as a condition of employment. This requirement is directly related to essential job functions including but not limited to: high-risk working environments (laboratories, clinical settings), handling hazards chemicals or lab specimens, conducting direct patient care, accessing medical and confidential records, access to prescription medication or other drugs, and job duties that can cause serious injury or death as a result of error. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.