Research Pharmacy Manager

Job Description

Job Description

Make a meaningful impact in oncology research and patient care.

We are seeking a dedicated Research Pharmacy Manager to oversee pharmaceutical operations that support cancer clinical trials. This leadership opportunity is ideal for a pharmacist who wants to combine clinical expertise with research management to advance life-changing therapies.

In this role, you will manage investigational drug protocols, maintain rigorous compliance with regulatory requirements, and guide teams in the safe and effective use of trial medications. Working closely with physicians, researchers, and care providers, you’ll help transform innovative science into better outcomes for patients.

If you are ready to elevate your pharmacy career and contribute to groundbreaking research in oncology, we would like to connect.

Compensation : $199,000 DOE

Responsibilities :

• Medication Oversight : Evaluate oncology and chemotherapy treatments for clinical trial participants, ensuring accurate dosing, administration, and managing potential side effects. Supervise the preparation and distribution of chemotherapy medications within acute care environments.
• Clinical Research Collaboration : Provide expert pharmacological advice and support for oncology-focused clinical trials, ensuring compliance with Good Clinical Practice (GCP) and all applicable regulatory standards. Prior experience in clinical research is a plus, but not essential.
• Adverse Event Monitoring : Track, document, and report any adverse events (AEs), severe adverse events (SAEs), adverse drug reactions (ADRs), medication errors, and drug interactions associated with investigational products in clinical trials.
• Regulatory Adherence : Assist in the development, review, and compliance with study protocols, ensuring adherence to regulations, particularly in relation to investigational drug management and regulatory inspections.
• Cross-functional collaboration : Partner with oncologists, research coordinators, nurses, and other healthcare professionals to ensure excellent patient care and clinical trial outcomes, while also attending related clinical meetings.
• Patient Education : Provide patients with clear information regarding their medication schedules, potential risks, benefits, and strategies for managing any side effects within the context of clinical trials.
• Data Management & Analysis : Contribute to the process of collecting, analyzing, and preparing data for clinical study reports, scientific publications, and regulatory submissions.
• Ongoing Education : Continuously update your knowledge of oncology treatments, clinical trial methodologies, and pharmaceutical research advancements through professional development opportunities, training, and conferences.

Qualifications :

Education : Doctor of Pharmacy (PharmD) degree from an accredited school of pharmacy.

Licensing : Valid and active pharmacist license in California.

Experience :

Certifications & Residency (Preferred but not required) :

Knowledge & Skills :

Personal Attributes :

Working Conditions :

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

About Company

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.

C-Clinical was not an act of compulsion, but the care one would have for family.

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.