Job Description

Job Description

Job Description

Oncology Research Pharmacist

An established research institution is seeking an experienced Oncology Research Pharmacist to support a growing portfolio of oncology clinical trials. This position offers the opportunity to apply advanced pharmacy knowledge within a mission-driven environment focused on improving cancer care through research and innovation.

In this role, you will work closely with physicians, investigators, and research personnel to ensure investigational medications are prepared, stored, and dispensed with full accuracy, safety, and compliance. Core responsibilities include reviewing and interpreting study protocols, managing drug accountability, maintaining complete documentation, and supporting regulatory requirements across each phase of assigned studies.

This is a meaningful opportunity to contribute to the development of emerging oncology treatments and support research efforts that have the potential to shape future patient outcomes. The ideal candidate brings strong attention to detail, a collaborative mindset, and a commitment to excellence in a research-driven setting.

Added Value

• Work directly with physicians, investigators, and multidisciplinary clinical teams
• Participate in advancing oncology research initiatives
• Support investigational drug development and study execution
• Ensure compliance with FDA, GCP, and institutional standards
• Join a respected research center focused on innovation and patient care

If you are a pharmacist who excels in research environments and is motivated to contribute to the future of oncology treatment, we would like to connect.

$200,000 DOE

• Medication Management : Assess chemotherapy and oncology medications for clinical trial patients, ensuring proper dosing, administration, and side effect management. Oversee compounding and dispensing of chemotherapy meds in acute care settings.
• Clinical Research Support : Provide pharmacological guidance for oncology clinical trials, ensuring compliance with GCP and regulatory guidelines. Clinical research experience is preferred but not required.
• Pharmacovigilance : Monitor and report adverse events (AEs), serious adverse events (SAEs), adverse drug reactions (ADRs), medication errors, and drug interactions for investigational products in clinical trials.
• Regulatory Compliance : Assist in protocol preparation, review, and adherence, including investigational drug management and regulatory inspections.
• Collaboration : Work with oncology investigators, research coordinators, nurses, and other professionals to ensure optimal patient care and study outcomes, attending relevant clinical meetings.
• Patient Education : Educate patients on medication regimens, risks, benefits, side effects, and management strategies within the context of clinical trials.
• Data Analysis & Reporting : Contribute to data collection, analysis, and preparation of clinical study reports, publications, and regulatory submissions.
• Professional Development : Stay up-to-date on oncology treatments, clinical trial methods, and pharmacological research through continuing education and relevant training.

Education:

• PharmD (Doctor of Pharmacy) from an accredited school of pharmacy.

Licensure:

• Active pharmacist license in California.

Experience:

• Minimum of 2 years of experience in oncology pharmacy practice.
• Experience with investigational drugs, chemotherapy regimens, and oncology clinical research preferred.

Certifications & Residency (preferred but not required):

• Board Certification in Oncology Pharmacy (BCOP) is highly desirable (to be considered for the high end of the salary).
• ASHP-accredited PGY-1 and PGY-2 residency in oncology or pain management is a plus.
• Clinical Research Certification (ACRP or SOCRA) is a plus.

Knowledge & Skills:

• Strong knowledge of oncology pharmacotherapy, including chemotherapy, biologics, targeted therapies, and immunotherapy.
• Strong communication, collaboration, organizational, and interpersonal skills.
• Familiarity with clinical trial protocols, regulatory requirements, and ethical guidelines is preferred.
• Proficiency with EHR/EMR systems and clinical trial management software is a plus.

Personal Attributes:

• Strong attention to detail with the ability to manage multiple projects simultaneously.
• Ability to work independently and collaboratively within a research team.
• Demonstrated commitment to patient safety and improving healthcare outcomes.

Working Conditions:

• Full-time, Monday to Friday, 9 am-5 pm with occasional travel (<10%) and overtime based on study needs.
• Work is conducted in a clinical research setting with direct patient interaction in a hospital or outpatient clinic.
• Must be currently located in Southern California.

Salary listed reflects the maximum amount, dependent on experience (DOE)

C-Clinical in Los Angeles drives clinical operations excellence across the pharmaceutical, biotechnology, and device sectors.

Our chief concept is in guiding relationships and directing the government. We go by "love" in the principle: love your neighbor as yourself, and charity.

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Bottom line - we created this company to do what we love to do: life-changing medical research, and to dedicate our time, talents, and resources to those who need them.

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