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At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.   📍  Location: Myrtle Beach, SC  | 🏥 Site Name: Trial Management Associates  | 🕒 Full-Time  | 🧪 Clinical Research Are you an experienced medical assistant or pharmacy tech looking to gain a new set of skills? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials. We’re seeking a Pharmacy Coordinator for our clinical research site located in Myrtle Beach, SC. The Pharmacy Coordinator plays a key role in the successful execution of pharmaceutical clinical trials by ensuring the safe, accurate, and compliant handling of the investigational products (IP)/drug that is being studied. Working under the supervision of a licensed pharmacist or nurse (as applicable), this individual will be responsible for receiving, storing, preparing, dispensing, documenting, and managing investigational drugs in accordance with study protocols, GCP/ICH regulations, and institutional SOPs. This role may also support administrative and data entry activities related to the conduct of clinical research.   Type:   Regular Full-time Employee Schedule:  Mondays through Thursdays 7:00 AM to 4:30 PM and Fridays 7:30 AM to 11:30 AM Location:   Onsite in Myrtle Beach, SC (no capabilities for remote or hybrid work) Reports to:  Site Director Benefits:   Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.   💼 What We Offer Competitive pay + annual performance incentives Medical, dental, and vision insurance 401(k) plan with company match Paid time off (PTO) and company holidays A mission-driven culture focused on advancing medicine and improving patient outcomes   🚀  Why Join Us? You’ll be part of a growing, mission-driven organization that values its people. At our core, we’re committed to bringing innovative medical treatments to patients faster—while creating an environment where employees thrive. If you’re passionate about clinical research and ready to make a difference, we’d love to hear from you.   Core Responsibilities: Investigational Product (IP) Management Receive, store, prepare, and dispense investigational products according to protocol, pharmacy manual, and regulatory requirements. Use IWRS/IRT systems to log shipments, assign IP, and perform returns or destructions per study-specific guidance. Maintain accurate inventory logs, temperature records, and expiration tracking for all IP and supplies. Monitor and respond to temperature excursions, discrepancies, or deviations per SOP. Perform aseptic preparations where required, following sterile technique protocols. Manage IP accountability documentation, including blinded and unblinded logs and reconciliation. Ensure all investigational product storage complies with GCP and institutional policies (double-locked, secure, labeled, etc.). Documentation & Compliance Maintain audit-ready records of all pharmacy activities, including temperature logs, equipment calibrations, and IP logs. Create and manage pharmacy study binders with updated regulatory and protocol-specific content. Adhere to ALCOA-C principles (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, and Consistent) in documentation pr