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Clinical Research Pre Screening Jobs in Nebraska

Celerion

Principal Investigator

Lincoln, NE

Celerion is committed to swift, exceptional clinical research through translational medicine. Every ... Pre-Study: Review protocol and Investigator Brochure for subject safety, scientific, and ...

Celerion

Principal Investigator

Lincoln, NE · On-site

Celerion is committed to swift, exceptional clinical research through translational medicine. Every ... Pre-Study: · Review protocol and Investigator Brochure for subject safety, scientific, and ...

Celerion

Principal Investigator

Lincoln, NE · On-site

Celerion is committed to swift, exceptional clinical research through translational medicine. Every ... Pre-Study: • Review protocol and Investigator Brochure for subject safety, scientific, and ...

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Clinical Research Pre Screening information

What is a clinical research pre screening specialist?

A Clinical Research Pre Screening specialist is responsible for evaluating potential participants to determine if they meet the basic eligibility criteria for clinical trials. They typically review medical histories, conduct initial assessments, and communicate with patients about the study requirements. This role is crucial in ensuring that only suitable candidates proceed to the next stages of the clinical trial process, which helps maintain the integrity and safety of the research. Pre screening specialists often work closely with clinical research coordinators and investigators.

What are the key skills and qualifications needed to thrive as a clinical research pre screening specialist?

To thrive as a Clinical Research Pre-Screening Specialist, you need a background in life sciences or healthcare, knowledge of research protocols, and attention to regulatory guidelines. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is often required. Strong interpersonal skills, attention to detail, and effective communication help in accurately evaluating candidates and collaborating with research teams. These skills ensure the accurate identification of eligible participants, compliance with study requirements, and smooth progression of clinical trials.

What are some common challenges faced by clinical research pre screening professionals, and how can they be addressed?

Clinical Research Pre-Screening professionals often face challenges such as accurately identifying eligible participants from large pools of applicants and ensuring strict adherence to study protocols and regulatory requirements. Managing sensitive patient data and maintaining clear communication with both clinical teams and potential participants can also be demanding. To address these challenges, it's important to stay organized, use standardized screening tools, and participate in regular training on compliance and privacy practices. Collaborating closely with research coordinators and maintaining up-to-date knowledge of study criteria can greatly improve efficiency and accuracy in pre-screening processes.

What is the difference between Clinical Research Pre Screening vs Clinical Research Coordinator?

AspectClinical Research Pre ScreeningClinical Research Coordinator
Primary RoleInitial participant eligibility assessment and screeningOversees entire study process, including recruitment, data collection, and follow-up
Required CredentialsHigh school diploma or equivalent; some roles may require clinical or research certificationsBachelor's degree in health or related field; often requires clinical research certification
Work EnvironmentScreening sites, clinics, or research facilitiesResearch sites, hospitals, clinics, or research institutions
Employer & Industry UsageUsed mainly during the participant recruitment phaseInvolved throughout the clinical trial lifecycle

While Clinical Research Pre Screening focuses on assessing participant eligibility at the start of a study, Clinical Research Coordinators manage the overall conduct of the trial, including recruitment, data collection, and compliance. Both roles are essential but differ in scope and responsibilities within the clinical research process.

What are popular job titles related to Clinical Research Pre Screening jobs in Nebraska?

For Clinical Research Pre Screening jobs in Nebraska, the most frequently searched job titles are:

What job categories do people searching Clinical Research Pre Screening jobs in Nebraska look for?

The top searched job categories for Clinical Research Pre Screening jobs in Nebraska are:

Clinical Research Pre Screening jobs near you

Clinical Research Assistant

Nebraska Cancer Specialists

Grand Island, NE

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 19 hours ago

Job description

Description

Nebraska Cancer Specialists is the regional leader in cancer diagnosis, treatment and research. With over 70 active clinical research studies, Nebraska Cancer Specialists is growing! We are seeking a Clinical Research Assistant in Grand Island to join our cutting edge, expanding, dedicated, inspiring and caring research team.


This position is responsible for assisting the research team in the implementation and conduct of clinical trials by performing tasks delegated by research team members.

What's in It for You? We know you work hard, and we believe in rewarding that! Here's what you'll love about NCS:

Monday-Friday schedule - No nights, weekends, or holidays!

Generous PTO - Plus holidays and your birthday off!

Affordable health, dental, and vision insurance

Employer-paid benefits - Short & long-term disability, life insurance, and EAP services

401(k), HSA, and FSA options - Plan for your future with confidence!

CEU/Conference allowance - Keep growing in your field!

Education Assistance - For Loans and Tuition

Extra perks - Because you deserve it


Position Summary

  • With supervision, ensures that clinical trials are conducted according to protocol.
  • Performs proper and accurate sample management, including collection, identification, transport, and/or processing of   biological (blood, urine, etc.) subject samples.
  • Manages study laboratory and shipping supplies.
  • Monitors and Records the temperatures of research dedicated refrigerators, freezers, and additional equipment.
  • Prepares and packages study specimens for shipment and manages package pickup.
  • Creates and maintains accurate records of all protocol activities and events, as delegated and trained.
  • Manages survival visit data entry, registry trials and imaging for patients on trial.
  • Requests tumor samples and schedules tumor biopsies.
  • Pre Screen patients for trial entry.
  • Participates in quality assurance of clinical research projects.

Requirements

  • Associate degree in a clinical or scientific related discipline required, bachelors or RN degree preferred.
  • Minimum of two years experience, clinical or scientific related discipline is required.  Oncology experience preferred.

Our team embodies our core values: Purpose, Innovation, Relationship and Excellence. NCS is an equal opportunity employer and participates in E-Verify.

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