Medical Assistant - Research Assistant

Myrtle Beach, SC – Full-Time | Mondays through Thursdays 7:00am-4:00pm | Fridays 7:30-11:30am

About the role

This is an exciting opportunity for recent graduates or experienced Medical Assistants to work directly with patients, support clinical trials, and build real-world skills alongside experienced research professionals. As a Clinical Research Assistant/Medical Assistant, you’ll play a key role in supporting study visits, interacting with patients, and ensuring research is conducted safely and accurately. Whether you're planning a future as a Clinical Research Coordinator, healthcare provider, or pursuing advanced education, this role provides a strong foundation and meaningful exposure to a fast-paced, patient-centered environment.

Responsibilities

• Study Preparation
  • Prepare and maintain study documents, including source charts, study binders, regulatory binders, and laboratory kits.
  • Schedule and confirm subject appointments, including ancillary visits such as diagnostic imaging and vendor-related services.
  • Understand study protocols, inclusion/exclusion criteria, and regulatory requirements, ensuring compliance with FDA, Sponsor, and Good Clinical Practice (GCP) guidelines.
  • Assist in participant recruitment by prescreening electronic medical records, following up on referrals, and coordinating outreach efforts.
• Participant Care and Interaction
  • Provide subject care, including explaining study procedures, answering questions, and monitoring diary compliance.
  • Conduct study procedures, such as collecting vital signs, performing ECGs, and completing study questionnaires.
  • Perform follow-up and reminder calls to ensure subject adherence to visits and study protocols.
  • Assist with participant stipend tracking and processing.
• Laboratory and Specimen Handling
  • Perform blood draws (phlebotomy) and process biological samples, including shipping per study requirements.
  • Maintain laboratory equipment, supplies, and temperature control systems, ensuring compliance with study protocols.
  • Generate and file weekly temperature reports for laboratory systems.
• Data Entry and Management
  • Enter and verify study data in Electronic Data Capture (EDC), Clinical Trial Management System (CTMS), and other databases.
  • Address system-generated queries and perform quality control checks to ensure data accuracy and completeness.
  • Assist with case report forms (CRFs) and source document completion, including query resolution under study coordinator guidance.
• Administrative and General Support
  • Maintain and organize participant charts, Investigator Site Files, and other regulatory documents.
  • Support clinical research coordinators (CRCs) by filing, scanning, and faxing required documents.
  • Clean, stock, and maintain exam rooms and department supplies to ensure readiness for participant visits.
  • Participate in investigator meetings, study teleconferences, and trainings.
  • Assist with onsite or remote clinical research monitor visits.

Requirements

• Bachelor's degree OR 2 years of college in a health-related program OR completion of a medical assistant, phlebotomist, or other healthcare-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP required.
• Certification as a Medical Assistant required.
• Experience with medical terminology and laboratory procedures helpful.
• Strong attention to detail, with the ability to collect, compile, and analyze patient data accurately.
• Excellent interpersonal, communication (verbal and written), and customer service skills.
• Ability to learn new computer or website applications (e.g., Electronic Medical Records, Clinical Trial Management Systems).
• Proven ability to prioritize tasks, meet deadlines, and adapt to a fast-paced work environment.
• Problem-solving skills with a proactive and solution-oriented approach.
• Strong organizational skills with the ability to prioritize tasks and meet strict deadlines.
• Phlebotomy training and experience heavily preferred; willingness to become fully trained required.

Skills

• Strong attention to detail and ability to follow step-by-step procedures.
• Ability to work efficiently in a fast-paced environment with changing priorities.
• Strong communication skills and a professional, patient-focused demeanor.
• Comfortable interacting with a diverse patient population.
• Proactive, dependable, and eager to learn new skills.
• Ability to balance multiple tasks and priorities throughout the day.

Benefits

• Gain hands-on experience working directly with patients in a clinical setting.
• Learn the fundamentals of clinical research and how trials are conducted.
• Build transferable skills for careers in healthcare, research, or biotechnology.
• Work alongside experienced professionals who provide training and mentorship.
• Create a strong foundation for advancement into roles like Clinical Research Coordinator or beyond.
• Make a meaningful impact by helping bring new treatments and therapies to patients.

Schedule

• Full-Time | Mondays through Thursdays 7:00am-4:00pm
• Fridays 7:30-11:30am