Clinical Research Pharmacist
We Fight Cancer: Care That Never Quits ®
Cancer Treatment Centers of America® (CTCA®) delivers an extraordinary patient experience we call Patient Empowered Care®. We deliver state-of-the-art, high quality care through an integrative model where a team of experts puts patients at the center of their own care. Every day, you will help patients win the fight against cancer. Every day is challenging and rewarding beyond your imagination.
A Culture of Teamwork, Empowerment & Development
CTCA provides Stakeholders with exceptional support and easy access to a wide range of tools and resources they need to bring the best of themselves, every day. Our benefits, wellness, and compensation programs lead the market. We also provide extensive training and career development opportunities that encourage professional and personal growth—it is a point of pride. We empower our Stakeholders to deliver the highest standard of care, which we call the Mother Standard®.
Prepares, compounds, manufactures, and dispenses investigational drugs and materials issued by the Investigational Drug Service for ongoing research studies. Manages required record-keeping, shipping, ordering, and inventory activities. Ensures the accuracy and integrity of products prior to their delivery to trial subjects. Ensures compliance with all applicable SERMC policies, governmental, and sponsor regulations, laws and policies related to the conduct of trials involving investigational or marketed drugs. Maintains records to meet sponsor requirements, FDA regulations and legal requirements for pharmacy operations. Creates SOPs and SWIs for the handling of investigational drugs. Creates order sets for each research study in SCM. Reviews all protocols and ensures that all ancillary staff is trained as it relates to the use of the investigational products or study treatments. Reads, interprets and processes orders for investigational drugs. Clarifies orders with prescribers as needed. Accurately dispenses medications and prepares sterile products, following proper aseptic and cytotoxic technique. Serves as a resource to the SERMC research community and healthcare professionals and to investigators in the development of investigator-initiated studies. Oversees the work performed by pharmacy technicians preparing investigational products to ensure that performance standards are maintained and that work is accurate and in accordance with state, federal and organizational regulations. Performs related responsibilities as required.
Key Position Qualifications
Graduate of an ACPE-accredited School of Pharmacy (RPh or Pharm D)
License in good standing as issued by the Georgia State Board of Pharmacy
Minimum of 5 years institutional pharmacy experience with oncology related experience
Minimum of 1 year experience working with investigational drug studies
The Best Place to Work
We call ourselves Stakeholders because we all have a stake in the care and success of every patient. Today, CTCA Stakeholders deliver healing and hope to patients fighting complex and advanced cancer in Atlanta, GA, Chicago, IL, Philadelphia, PA, Phoenix, AZ and Tulsa, OK. Each of our hospitals, and corporate entities, earned a Best Place to Work distinction and receives numerous accreditations that celebrate our culture of clinical quality, innovation, high performance and wellness.
Beyond The Resume, What We Look For
We select people with talent—people who value working with others and thrive in an environment of continuous improvement. We are creative and resourceful problem solvers. We are inventors and innovators. As a CTCA Stakeholder, you make the difference in the life of a patient. Do you see yourself working with a passionate team in a dynamic, high growth environment? If so, we hope you begin the application process, today.