Additional Info

1. Performs research procedures associated with clinical research including assessment and evaluation of patient needs. Coordinates patient participation in investigational protocols under the principal investigator’s direction. Facilitates the process of informed consent and enrollment of the patient to the study. (E)
2. Educates participants about the study including the daily requirements and informs of possible effects and outcomes. (E)
3. Plans and coordinates the patient evaluation and visits for protocols. Coordinates study patient’s visits, laboratory and clinic appointments to ensure that procedures are performed according to protocol. (E)
4. Serves as primary contact for assigned research trials. Provides direct care under the principal investigator’s direction for participants in compliance with investigational protocols. (E)
5. Evaluates progress of each research trial and reports weekly to the Principal Investigator. (E)

1. Maintains regulatory documents and case report forms accurately in compliance with FDA guidelines. (E)
2. Interacts with research pharmacists to maintain adequate supplies and records of investigational drugs. (E)
3. Coordinates the collection, processing and distribution of laboratory samples to labs as designated. (E)
4. Assists principal investigator with IRB applications, requests for change in protocols, annual reviews and adverse event reporting. (E)
5. Assures accurate research billing as required by UNMC/ NMC policies, using either hospital information or UNMC billing programs, and auditing those charges as they are logged. (E)
6. Assists with site qualification visits, site initiation visits and setting up monitor visits. (E)

1. Maintains complete and confidential patient files on each participant. (E)
2. Completes surveys, database information and/or case report forms in a timely manner with high degree of accuracy. (E)

1. Assists in establishing and implementing patient education programs for dermatologic-related medical conditions (E)
2. Assists in establishing and implementing medication education for patients. (E)
3. Educate patients of possible side effects, in accordance with specific study protocols. (E)
4. Instructs patients in basic prevention programs. (E)

Other Duties As Assigned

• Effective communication and interpersonal skills.
• Ability to work effectively with other team members
• Solid organizational skills.
• Attention to detail and accuracy
• Knowledge of current nursing procedure, techniques, and practices
• Able to do physical assessment as appropriate.
• Computer literacy and proficience.
• Utilization of knowledge and skills related to meeting age-specific needs of patient population served within the scope of the job description. Age specific populations served include Adult (18-65) and Geriatric (65 and older).

• Determines patient eligibility and ensures protocol compliance for clinical and translational research studies.

• Uses clinical judgment to monitor participant safety and respond to adverse events or protocol deviations.

• Coordinates study logistics, including scheduling, data collection, and documentation accuracy.

• Serves as liaison between investigators, sponsors, regulatory offices, and clinical staff.

• Troubleshoots operational issues to maintain study timelines and integrity.

• Educates participants about study procedures and ensures informed consent is properly obtained.

• Balances research requirements with patient care priorities in an academic dermatology setting.

• Serves as a key link between clinical care, research, and regulatory compliance, ensuring that departmental research aligns with institutional and federal standards.

• Directly influences the department’s ability to participate in and expand clinical trials, enhancing the institution’s research reputation and patient care offerings.

• Supports faculty and investigators by facilitating efficient study operations, improving research productivity, and enabling access to innovative dermatologic treatments.

• Impacts patient outcomes and safety by ensuring ethical conduct, accurate data collection, and adherence to research protocols.

• Contributes to the broader campus community by promoting collaboration across departments, mentoring students or trainees involved in research, and advancing UNMC’s academic mission through high-quality clinical research.

Determined within a relatively short period of time

Responsible for assisting in working with PI and Administrator on initial budgets with the CRC.

This person’s decision making and problem solving skills can directly affect the health and well-being of study patients. In addition, the protocols performed and the data collected will have a significant impact on the validity of the study results.

Department Administrator will supervise this person. PIs will also help supervise them on clinical trials.

No

N/A

Office,Clinical

Adult (18-65 years),Geriatric (65 and older)

N/A

N/A

N/A

Protective eye wear Full extent of exposures TBD by academic and research activities.

N/A