Clinical Research Coordinator

Clinical Research Coordinator

Dell Medical School is seeking a Clinical Research Coordinator. This is a grant-funded position that has an end date of 12/31/27, renewable based upon availability of funding, work performance, and progress toward research goals. Flexible work hours (including weekend and/or after hours) to meet deadlines.

The Clinical Research Coordinator manages day-to-day study operations under the direction of a Principal Investigator (PI), ensuring protocol fidelity, participant safety, data integrity, and regulatory compliance across start-up, conduct, and close-out activities. Typical partnerships include investigators, research nurses, pharmacists, laboratory teams, radiology, billing/compliance, and sponsor/CRO monitors; the role commonly reports to a PI, Research Manager, or equivalent. This role will serve in the Department of Psychiatry and Behavioral Sciences aiding in bipolar disorder research. Employee must be willing to work on weekends/after normal business hours to meet deadlines, when needed.

Responsibilities include coordinating study start-up and feasibility, recruiting, screening, and consenting participants, planning and conducting study visits, ensuring participant safety and reporting, managing regulatory and ethics documentation, overseeing data quality and monitoring, coordinating site operations and stakeholder communication, and conducting study close-out.

Knowledge, skills, and abilities include managing and measuring work, functional/technical skills in clinical research operations, interpersonal savvy, decision quality, planning and priority setting, ethics and compliance, and learning agility.

Education and experience requirements include a Bachelor's Degree in health, psychology, neuroscience, life science, or a related field with at least 3 years of experience in clinical research coordination or closely related human-subjects research experience. Relevant education and experience may be substituted as appropriate. Preferred qualifications include a Master's Degree in nursing, allied health, psychology, neuroscience, public health, biology, pharmacology, or a related field with at least 1 year of experience in coordinating interventional trials.

Salary range is $53,464+ depending on qualifications. Working environment includes standard office equipment, repetitive use of a keyboard, and may work around biohazards.

Required materials include a resume/CV, 3 work references with their contact information; at least one reference should be from a supervisor, and a letter of interest.

Tagged as: Life Sciences