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Clinical Research Pre Screening Jobs in Nebraska

Celerion

Clinical Research Coordinator

Lincoln, NE · On-site

$50 - $70/hr

... pre-study, in-process and post study review, problem solving as needed during study conduct ... Clinical Research experience useful, but not required. Celerion Values: Integrity Trust Teamwork ...

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

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 Coordinator

Grandisland

Grand Island, NE • On-site

$52 - $75/hr

Other

This job post has expired 2 days ago. Applications are no longer accepted.

Job description

Velocity Clinical Research is seeking a highly organized, patient-focused Clinical Research Coordinator (CRC) to manage and conduct clinical trials in accordance with study protocols, Good Clinical Practice (GCP), ICH guidelines, and company Standard Operating Procedures (SOPs). The CRC serves as the primary liaison between study participants, investigators, sponsors, CROs, and site staff while ensuring subject safety, protocol compliance, and data integrity throughout the research process.

Key Responsibilities
  • Coordinate all assigned clinical trials from study start-up through closeout.
  • Recruit, pre-screen, and schedule study participants.
  • Conduct informed consent discussions and study visits.
  • Perform protocol-required procedures within scope of training, including vital signs, ECGs, specimen collection, processing, and investigational product administration when applicable.
  • Maintain accurate source documentation and enter study data into sponsor electronic data capture systems.
  • Resolve data queries and ensure timely, high-quality data submission.
  • Monitor and report adverse events, serious adverse events, and protocol deviations according to protocol and regulatory requirements.
  • Collect, maintain, and submit regulatory documentation to sponsors and IRBs.
  • Coordinate study vendors and ensure protocol requirements are met.
  • Train and support delegated study staff as appropriate.
  • Maintain patient confidentiality and protect sponsor and company confidential information.
  • Collaborate effectively with investigators, patients, sponsors, CROs, and internal team members.
Qualifications
  • Strong understanding of medical terminology.
  • Excellent organizational, communication, and multitasking abilities.
  • Ability to work independently and in a fast-paced environment.
  • Proficiency with Microsoft Office applications and electronic data systems.
  • Detail-oriented with strong problem-solving skills.
  • Commitment to patient safety and research quality.

The ideal candidate is compassionate, detail-oriented, adaptable, and passionate about advancing medicine through clinical research. They enjoy working directly with patients while managing multiple studies and timelines with accuracy and professionalism.

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