What are the responsibilities and job description for the Clinical Research Coordinator position at Epic Medical Research?
Company Description Epic Medical Research partners with sponsors to accelerate the development and delivery of new therapies through rigorous science and data-driven solutions. The organization operates clinical trial sites in Alabama, Arizona, Louisiana, New Jersey, and Oklahoma, providing access to diverse participant populations. A skilled team uses advanced research methodologies and analytics to examine social, cultural, and biological factors that influence health outcomes. This approach supports the generation of robust, high-quality data for effective treatment development and healthcare innovation. Epic Medical Research is committed to improving health and well-being in diverse communities while helping sponsors bring better treatments to market.
Role Description The Clinical Research Coordinator is a full-time, on-site role based in Monroe, LA. This position is responsible for coordinating day-to-day Oncology clinical trial activities, including participant screening, enrollment, and follow-up in accordance with study protocols and regulatory requirements. The role includes obtaining and documenting informed consent, scheduling and conducting study visits, collecting and entering data, and maintaining accurate study records. The Clinical Research Coordinator will collaborate with investigators, sponsors, and site staff to ensure protocol adherence, participant safety, and timely completion of study milestones. Additional responsibilities may include managing regulatory documents, preparing for monitoring visits, and supporting quality assurance processes.
Qualifications
- Candidates should possess skills in clinical trial conduct, including Protocol understanding and Clinical Trials coordination.
- Candidates should possess skills related to participant enrollment and ethics, including Informed Consent and Research involving human participants.
- Candidates should possess Clinical Research Experience, with familiarity in regulatory compliance and good clinical practice (GCP)
- Strong organizational and time-management skills, with attention to detail and accuracy in documentation.
- Effective written and verbal communication skills, with the ability to interact professionally with participants, investigators, and sponsors.
- Proficiency in basic computer applications and electronic data capture systems; experience with EMR or CTMS is an advantage.
- Ability to work on-site in Monroe, LA, manage multiple studies concurrently, and uphold participant safety and confidentiality.