Clinical Informatics Coordinator jobs in Nebraska

Quality Clinical Research is a dynamic and innovative research organization dedicated to advancing medical science and improving patient care. We are committed to conducting cutting-edge clinical research across a wide range of therapeutic areas. Our team of dedicated professionals works collaboratively to bring novel treatments and therapies to the patients who need them most.

Job Description:

We are seeking a highly motivated and organized Clinical Research Coordinator to join our team. The successful candidate will play a crucial role in the execution and management of clinical research studies, ensuring adherence to protocol and regulatory guidelines. If you have a passion for making a difference in patient care and are committed to the highest standards of research integrity, we want to hear from you.

Key Responsibilities:

Coordinate all aspects of clinical research studies from initiation to close-out.

Work closely with the Principal Investigator and other team members to develop and implement research protocols.

Recruit, screen, and enroll eligible study participants, obtaining informed consent.

Collect, record, and manage study data with a strong attention to detail and data accuracy.

Ensure compliance with all regulatory requirements and ethical standards.

Collaborate with research sponsors, monitors, and study participants to provide ongoing support and communication.

Schedule and facilitate study-related visits, tests, and procedures.

Prepare and submit documentation to regulatory authorities and ethics committees.

Maintain study documentation and source records in accordance with Good Clinical Practice (GCP) standards.

Monitor and maintain inventory of study supplies and investigational products.

Assist with the preparation of reports and presentations for research findings.

Assist with the management of budgets and financial aspects of clinical trials.

Qualifications:

MA, LPN,RN

Previous experience as a Clinical Research Coordinator is preferred.

Knowledge of clinical research regulations and GCP guidelines.

Strong organizational and time management skills.

Excellent interpersonal and communication skills.

Proficiency in Microsoft Office suite and electronic data capture systems.

Ability to work both independently and as part of a team.

Detail-oriented and capable of multitasking.

Ability to travel for Clinic activities, attend investigator meetings, or vendor visits/audits, as required.

Familiar with the background of the study drug and requirements of the study

Have high ethical standards and professional honesty

Friendly and outgoing demeanor

Must demonstrate a passion for direct patient interaction

Demonstrate clinical competence, positive leadership, and ability to work collaboratively with a multi-disciplinary team

Prolonged periods of sitting at a desk and working on a computer

Must be able to lift 15 pounds at times

Picking, pinching, typing or otherwise working, primarily with fingers rather than with whole hand or arm as in handling

Talking: Expressing or exchanging ideas by means of the spoken word; those activities where detailed or important spoken instructions must be conveyed to other workers accurately, loudly, or quickly

Hearing: Perceiving the nature of sounds at normal speaking levels with or without correction, and having the ability to receive detailed information through oral communication, and making fine discrimination in sound

The worker is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal; extensive reading; visual inspection involving small defects, small parts, and/or operation of machines (including inspection); using measurement devices; and/or assembly or fabrication of parts at distances close to the eyes

Why Join Quality Clinical Research?

Be part of a dynamic team dedicated to advancing medical science.

Opportunity for professional growth and development.

Competitive salary and benefits package.

Contribute to cutting-edge research that can improve patient care.

If you are passionate about clinical research and want to make a meaningful impact, we encourage you to apply. To be considered for this role, please submit your resume, a cover letter, and any relevant certifications.

Currently, we are not providing a relocating stipend. Must be able to work in the Omaha area

Quality Clinical Research is an equal opportunity employer and welcomes candidates from diverse backgrounds.