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Clinical Research Pre Screening Jobs (NOW HIRING)

Actalent

Clinical Research Coordinator

Philadelphia, PA · Hybrid

$28 - $31.25/hr

Clinical Research Coordinator This role supports cutting-edge oncology clinical trials by ... Recruit, pre-screen, and enroll patients into oncology clinical trials in accordance with study ...

Actalent

Clinical Research Coordinator

Norfolk, NE

$25 - $33/hr

Job Title: Part-Time Clinical Research Coordinator Hours: 20 per week (flexible Monday-Friday ... Conduct pre-screening of potential participants, verifying eligibility based on medical history ...

Actalent

Clinical Research Nurse

Mobile, AL

$25 - $35/hr

Conduct pre-screening of patients and chart reviews. Essential Skills * Minimum of 2 years of experience as a Clinical Research Nurse. * Oncology clinical trial experience. * Proficiency in ...

New

Actalent

Clinical Research Nurse

Norfolk, NE

$25 - $33/hr

Clinical Research Nurse Hours: 20 per week (flexible Monday-Friday) Duration: Contract through ... Conduct pre-screening of potential participants, verifying eligibility based on medical history ...

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Clinical Research Pre Screening information

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How much do clinical research pre screening jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for clinical research pre screening in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

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, and why are they important?

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 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 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.
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Clinical Research Pre Screening jobs near you
Infographic showing various Clinical Research Pre Screening job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 73% Full Time, 17% Part Time, and 9% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $47,241 per year, or $22.7 per hour.
Clinical Research Investigator (MD/DO)

Clinical Research Investigator (MD/DO)

DM Clinical Research

Charlotte, NC

$45K - $45K/yr

Full-time

Posted 14 days ago

Job description

Clinical Research Investigator (MD/DO)
DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 in the country, is looking for an Investigator for our site in Charlotte, NC. This individual will conduct all clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes.
Responsibilities
  • Ensures the medical well-being and safety of the participants through the safe performance and execution of the studies.
  • Assists in maintaining clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site.
  • Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants.
  • Interprets protocols and IB and participates in initiatives to strategize for patient recruitment.
  • Carries out clinical evaluation and assessment of participants to ensure eligibility to enroll in studies.
  • Ensures and protects the welfare and safety of participants through ethical conduct.
  • Fulfills and complies with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations.
  • Exercises meticulous attention to detail in documentation and patient care.
Requirements
  • Medical license (MD, DO) - Charlotte, NC
  • 2 years experience as a Clinical Research Investigator (Principal Investigator or Sub-Investigator)
  • Bilingual Spanish a plus
Flexible hours - schedule can be tailored as required.

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