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Laboratory Coordinator / Phlebotomist

Headlands Research
CompanyHeadlands Research
CategoryHealthcare
LocationMyrtle Beach
RemoteOn-site (inferred)
EmploymentNot stated
LevelNot stated
SalaryNot stated by the employer
Posted10 Jul 2026
Last verified5 Aug 2026
SourceEmployer ATS (greenhouse)
Applications are handled by the employer, not by us.Apply on the employer's site →
Description
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.     📍  Myrtle Beach, SC 🏥  Trial Management Associates 🕒  Full-Time | Monday through Friday   Looking for more than just high-volume blood draws? If you’re a phlebotomist or lab technician who takes pride in precision, patient care, and doing things the  right  way—not just the fast way—clinical research may be the next step in your career. At  Trial Management Associates , our lab professionals work in a  structured, calm, and purpose-driven environment , supporting clinical trials that help advance new treatments for psychiatric, dementia, and memory-related conditions.   Why Lab Professionals Choose Clinical Research Predictable weekday schedule  (no nights, no weekends, no emergency draws) More time and control  during patient visits and specimen handling Specialized lab work  beyond routine phlebotomy (processing, PK handling, shipping) Smaller, collaborative teams  where your role is respected Meaningful purpose —your work directly supports future medical treatments This role is ideal for lab professionals who value  accuracy, organization, and consistency , and who want to grow their skills beyond traditional lab or hospital settings.   The Role The Phlebotomist/Lab Tech is a key member of the clinical research team, supporting studies through  specimen collection, processing, documentation, and shipment  in compliance with Good Clinical Practice (GCP), study protocols, and safety regulations. You’ll work in a controlled clinical research environment with  scheduled visits, detailed protocols, and strong operational support , allowing you to focus on quality and precision.   Who Thrives in This Role Lab professionals who value  precision over speed Phlebotomists looking for  predictability and balance Candidates curious about clinical research and career growth Team players who take pride in quality, compliance, and patient experience   Responsibilities: Perform phlebotomy, urine collection, and sample processing (centrifuging, aliquoting, labeling). Prepare lab kits for each subject based on study protocols. Ship biological specimens following IATA guidelines and protocol requirements. Maintain specimen logs, shipping records, temperature logs, and other documentation. Conduct point-of-care tests (e.g., urine drug screens, pregnancy tests). Assist with patient procedures including vital signs, ECGs, and physical/neurological exam setups. Clean and sanitize lab equipment and work areas daily. Perform and document equipment calibration and ensure safety compliance (OSHA, HIPAA). Accurately record lab results and maintain electronic and paper logs in systems such as CRIO or eCRFs. Respond to and resolve electronic data queries. Verify accuracy and completeness of data entries and study documentation. Participate in quality control and assurance initiatives to ensure regulatory compliance. Monitor and maintain inventory of lab kits and supplies. Order dry ice and other lab necessities. Destroy expired kits and log per protocol. Support preparation of study-specific training materials and lab manuals. Collaborate with study coordinators and medical staff to meet visit protocol requirements. May assist with infusion monitoring under clinician supervision.   Requirements: Must be certified in phlebotomy Previous healthcare experience preferred; dire
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