Investigational Pharmacist Job at C-Clinical at Los Angeles, Los Angeles, CA

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  • C-Clinical at Los Angeles
  • Los Angeles, CA

Job Description

Job Description

Job Description

Investigational Pharmacist Opportunity

Be part of a forward-thinking research organization that’s shaping the future of medicine. As an Investigational Pharmacist, you’ll be at the center of groundbreaking clinical trials, ensuring every study runs with precision, compliance, and the highest level of patient safety.

In this full-time role, you’ll work alongside investigators, clinicians, and study coordinators to oversee investigational drug preparation, labeling, dispensing, and accountability. Your attention to detail and commitment to excellence will help advance innovative therapies and contribute to improved outcomes for patients everywhere.

What You’ll Do:

  • Manage investigational products in accordance with study protocols and regulations
  • Ensure accurate preparation, labeling, and documentation for all study medications
  • Collaborate closely with physicians and research teams to maintain protocol integrity
  • Monitor inventory, temperature logs, and chain-of-custody requirements
  • Promote patient safety through best practices in storage, dispensing, and compliance

What We’re Looking For:

  • Licensed pharmacist with strong clinical and regulatory knowledge
  • Experience in investigational or clinical research pharmacy preferred
  • Exceptional organizational and problem-solving abilities
  • Comfortable communicating and collaborating across multidisciplinary teams
  • Driven by precision, ethics, and a passion for advancing patient care
Compensation:

$195,000 yearly

Responsibilities:
  • Medication Oversight: Ensure proper dosing and administration of oncology treatments, manage side effects, and supervise chemotherapy medication preparation in acute care settings.
  • Clinical Research Collaboration: Provide pharmacological support for oncology trials, ensuring compliance with regulatory standards.
  • Adverse Event Monitoring: Track and report adverse events, drug reactions, and interactions related to investigational products.
  • Regulatory Adherence: Assist with protocol development and ensure compliance with investigational drug management regulations.
  • Cross-Functional Collaboration: Work closely with oncologists, nurses, and research staff to ensure patient care and successful trial outcomes.
  • Patient Education: Educate patients on medication regimens, risks, benefits, and side effect management.
  • Data Management & Analysis: Support data collection, analysis, and report preparation for clinical studies and regulatory submissions.
  • Ongoing Education: Stay updated on oncology treatments and clinical trial advancements through professional development.
Qualifications:
  • Education: Doctor of Pharmacy (PharmD) from an accredited pharmacy school.
  • Licensing: Active pharmacist license in California.
  • Experience: Minimum of 2 years 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.
  • ASHP-accredited PGY-1 and PGY-2 residency in oncology or pain management is a plus.
  • Clinical Research Certification (ACRP or SOCRA) is beneficial.
  • Knowledge & Skills: Strong understanding of oncology pharmacotherapy, including chemotherapy, biologics, targeted therapies, and immunotherapy.
  • Excellent communication, organizational, and collaboration skills.
  • Familiarity with clinical trial protocols, regulatory guidelines, and ethical standards is preferred.
  • Proficiency in EHR/EMR and clinical trial management software is advantageous.
  • Personal Attributes: Exceptional attention to detail and the ability to handle multiple projects.
  • Strong independent work ethic while collaborating effectively with research teams.
  • Commitment to patient safety and continuous healthcare improvement.
  • Working Conditions: Full-time, Monday to Friday, 9:00 AM to 5:00 PM, occasional travel (less than 10%), and potential overtime based on study needs.
  • Work in clinical research settings with direct patient interaction, either in hospitals or outpatient clinics.
  • Must reside in Southern California.

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.

Job Tags

Full time, Monday to Friday,

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