Clinical Research & Data Coordinator Full Time NEW

Morehouse School of Medicine is seeking a highly motivated, detail-oriented Clinical Research & Data Coordinator to support the Precision Medicine Implementation studies, like the Tulisokibart for Moderate to Severe Ulcerative Colitis Study. This pivotal role is responsible for facilitating the timely and accurate matching of participants to appropriate clinical trials, with an emphasis on leveraging electronic health records (EHRs) for participant identification and data management. The coordinator will oversee key aspects of clinical trial operations and assist with ensuring seamless and secure access to and utilization of clinical data. This includes managing study participant data, preparing for rapid clinical trial study activations, ensuring data integrity, and serving as a liaison between physicians, research teams, and other stakeholders. This position plays a vital role in advancing clinical research and improving patient access to clinical trials. REPORTS TO: Principal Investigator, Tulisokibart for Moderate to Severe Ulcerative Colitis Study KNOWLEDGE , SKILLS , & ABILITIES : Strong understanding of clinical research processes and human subjects research and protections. Understanding of clinical data, including data structures, standards, and ontologies29292929. Familiarity with oncology trials and precision medicine concepts, particularly related to genomic testing and clinical trial matching. Working knowledge of electronic health records (EHRs), clinical trial management systems ( CTMS ), and data entry protocols. Awareness of ethical considerations related to the informed consent process and data privacy33. Also, familiarity with regulatory and ethical aspects of clinical research, including Good Clinical Practice ( GCP ) guidelines, Institutional Review Board ( IRB ) procedures, and Health Insurance Portability and Accountability Act ( HIPAA ) regulations. Ability to build and maintain positive working relationships across interdisciplinary teams. Ability to adapt quickly to changes in program needs, study protocols, and technology platforms. Ability to manage multiple tasks and projects simultaneously, set priorities, and meet deadlines. Ability to maintain confidentiality and protect sensitive patient and research data, upholding ethical standards and complying with all regulations applicable to clinical research. CORE COMPETENCIES : Clinical Research Coordination: Understands clinical trial protocols, workflows, and regulatory compliance and coordinates multiple study components with precision and timeliness. Attention to Detail: Demonstrates accuracy in data entry, documentation, and review; identifies and resolves discrepancies in patient records and study data. Communication: Communicates clearly and effectively with internal and external stakeholders, including physicians, patients, and research staff, adapting messaging based on the audience and context (e.g., written, verbal, or electronic). Collaboration & Teamwork: Builds productive relationships across departments and with partner organizations and demonstrates a cooperative approach and willingness to support team goals. Patient-Centered Focus: Prioritizes patient safety, privacy, and access to appropriate clinical trials and demonstrates cultural sensitivity and empathy in patient interactions. Problem-Solving & Critical Thinking: Identifies operational challenges and proposes practical, evidence-based solutions; anticipates potential issues and takes proactive steps to minimize disruptions. Time Management & Adaptability: Manages shifting priorities in a dynamic research environment and remains flexible and calm under pressure, especially during rapid study activations. Ethical Conduct & Integrity: Upholds institutional and regulatory standards related to clinical research and handles confidential data responsibly, and adheres to ethical principles. Technology Proficiency: Navigates clinical databases, electronic health records (EHRs), and research software efficiently and learns new digital tools and platforms as needed for trial coordination. Project Management: Demonstrates experience in coordinating and managing projects, ensuring objectives are met within set timeframes. Able to identify and allocate resources effectively and can anticipate and mitigate potential risks or delays. SUPERVISORY RESPONSIBILITIES : This position will not have any supervisory responsibilities.

Minimum Qualifications

Education High School Diploma or GED and three years of clinical research experience. OR Two years of college in a scientific, health-related, or business administration program and one year of clinical research experience. OR Licensed as a practical nurse ( LPN ) and with one year of clinical research experience. OR Bachelor’s degree, Master’s degree, MD or PhD in a scientific, health-related or business administration program. Experience Minimum 2-3 years of experience working with clinical data, particularly in a research or healthcare setting. MS Office Suite. Ability to prioritize tasks and work independently, as well as part of a multi-disciplinary team.

Preferred Qualifications

Familiarity with EHR data standards, data integration, and the ethical/legal considerations surrounding data usage. Excellent analytical, problem-solving, and organizational skills. Superior communication skills, both written and verbal. MS Office Suite.

Description of Job Duty

POSITION ACCOUNTABILITIES AND ESSENTIAL FUNCTIONS : Study Participant Management: Oversee the electronic health records (EHRs) to identify & match study participants and screen and enroll study participants for available clinical trials. Clinical Data Management : Manage clinical trial data sets, ensuring accuracy, consistency, and security. Ensure that all clinical trial data are accurately entered into electronic data capture ( EDC ) systems and in a timely manner, adhering to established protocols and guidelines. Study Coordination : Collaborate with researchers and physicians to implement health informatics solutions that support the enrollment of clinical trial participants. Study Compliance and Data Integrity : Maintain data standards, ontologies, and metadata frameworks in alignment with best practices and regulatory requirements. Ensure adherence to clinical trial regulatory requirements ( IRB , HIPAA , GCP , etc.). Data Analysis : Assist with data visualization and communication of clinical and real-world data to various stakeholders. Collaboration : Contribute to the drafting of manuscripts, reports, and grants, as well as present findings at scientific meetings and conferences.