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Clinical Drug Screening Associate Jobs (NOW HIRING)

Frontage Laboratories

Clinical Research Nurse

Secaucus, NJ · On-site

$45 - $55/hr

Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK ... Assists in the screening of research subjects to evaluate their eligibility for a clinical study.

Beacon Hill

Clinical Trial Associate

Cambridge, MA · Hybrid

$36.50 - $50/hr

Clinical Trial Associate Contract Term: 6 months to start; could extend Hybrid - 3 days onsite ... clinical drug development Experience with regulatory affairs, including IND/CTA submissions ...

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Clinical Drug Screening Associate information

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$12

$31

$55

How much do clinical drug screening associate jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for clinical drug screening associate in the United States is $31.54, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $41.59 per hour, depending on experience, location, and employer.

What are some common challenges faced by Clinical Drug Screening Associates, and how can they be managed effectively?

Clinical Drug Screening Associates often encounter challenges such as maintaining strict adherence to chain-of-custody protocols and managing high sample volumes while ensuring accuracy. Effective time management, meticulous attention to detail, and clear communication with both laboratory staff and healthcare providers are essential to overcoming these challenges. Continuous training on compliance and regularly reviewing standard operating procedures can also help associates maintain high-quality results and minimize errors in a fast-paced environment.

What does a Clinical Drug Screening Associate do?

A Clinical Drug Screening Associate is responsible for collecting, processing, and analyzing biological samples—such as urine, blood, or saliva—for the presence of drugs or other substances. They ensure that testing procedures follow strict protocols to maintain accuracy and confidentiality. Additionally, they document results, communicate findings to relevant healthcare professionals, and may assist with quality control and regulatory compliance. This role is essential in healthcare, employment, and legal settings where drug testing is required.

What are the key skills and qualifications needed to thrive as a Clinical Drug Screening Associate, and why are they important?

To thrive as a Clinical Drug Screening Associate, you need a solid understanding of laboratory procedures, attention to detail, and knowledge of clinical testing protocols, usually supported by a degree in a life science or related field. Familiarity with laboratory information management systems (LIMS), specimen handling tools, and relevant certifications like CLIA or ASCP are typically required. Strong organization, communication, and problem-solving skills help you manage samples efficiently and ensure accurate reporting. These competencies are vital for maintaining the integrity of drug screening processes and ensuring reliable results for patient care and regulatory compliance.

What is the difference between Clinical Drug Screening Associate vs Laboratory Technician?

AspectClinical Drug Screening AssociateLaboratory Technician
CertificationsOften requires certification in drug testing or related fieldsMay require general laboratory certifications or degrees
Work EnvironmentHealthcare or clinical settings, focusing on drug screening processesLaboratories across various industries, including healthcare, research, and manufacturing
Job ResponsibilitiesCollecting samples, conducting drug tests, recording resultsPreparing samples, operating lab equipment, data entry

The Clinical Drug Screening Associate and Laboratory Technician roles share similarities in laboratory work and certifications. However, the associate focuses specifically on drug screening in clinical settings, while the technician may work across broader laboratory functions. Both roles are essential in healthcare and research industries, often requiring related certifications and work environments.

More about Clinical Drug Screening Associate jobs
What cities are hiring for Clinical Drug Screening Associate jobs? Cities with the most Clinical Drug Screening Associate job openings:
What states have the most Clinical Drug Screening Associate jobs? States with the most job openings for Clinical Drug Screening Associate jobs include:
What job categories do people searching Clinical Drug Screening Associate jobs look for? The top searched job categories for Clinical Drug Screening Associate jobs are:
Clinical Drug Screening Associate jobs near you
Infographic showing various Clinical Drug Screening Associate job openings in the United States as of June 2026, with employment types broken down into 6% As Needed, 49% Full Time, 29% Part Time, 1% Temporary, and 15% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $65,604 per year, or $31.5 per hour.

Clinical Research Assistant

Prolerity Clinical Research

Houma, LA • On-site

Full-time

Posted 22 days ago

Job description

Description:

The Clinical Research Assistant (CRA) assists in the daily activities of clinical research studies and clinic operations. This role involves working closely with clinical teams, investigators, and study participants to ensure that all required procedures and visits occur according to protocol-specific guidelines.


Key Responsibilities:

  • Study Familiarization: Thoroughly understand assigned studies by reading protocols, attending start-up meetings, and coordinating with the Principal Investigator and study team.
  • Protocol Adherence: Ensure strict adherence to study protocols and obtain exemptions when applicable.
  • Specimen Collection & Processing: Collect, process, and ship laboratory samples in accordance with study requirements.
  • Patient Screening & Qualification: Collect initial psychiatric and medical information through patient interviews and access appropriate sources to qualify and accurately place patients in enrolling clinical trials.
  • Study Coordination Support: Assist Clinical Research Coordinators in trial-related organization and documentation, including filing and maintaining regulatory records.
  • Communication & Reporting: Communicate protocol issues to the study team, Site Administrator, Principal Investigator (PI), or Sub-Investigator as needed.
  • Clinical Tasks: Perform clinical tasks such as vital signs measurement, height and weight recording, ECG administration, phlebotomy, and specimen packaging.
  • Documentation & Compliance: Maintain timely source documentation and ensure compliance with sponsor-required information.
  • Patient Education: Educate patients and their families about study participation and clinical drug trials in general.
  • Community Engagement: Assist in community outreach events and provide appropriate community resource referrals to patients, caretakers, and family members when applicable.
  • Additional Duties: Perform ad-hoc tasks and assist in other study-related activities as needed.

Additional Responsibilities:

This job description outlines the primary responsibilities of the Clinical Research Assistant; however, additional duties may be assigned as needed to support the research program or the operational needs of the organization. These additional responsibilities are not limited to the above and may evolve over time based on study requirements or business needs.

Requirements:

Knowledge, Skills, and Abilities:

  • Communication: Ability to communicate effectively (both written and oral) with patients, study teams, and external stakeholders.
  • Interpersonal Skills: Excellent interpersonal and customer service skills to engage with study participants and colleagues.
  • Organizational Skills: Strong ability to prioritize tasks, manage multiple responsibilities, and maintain documentation.
  • Technical Proficiency: Proficiency in Microsoft Office software required; knowledge of Electronic Medical Records (EMR) systems preferred.
  • Attention to Detail: High level of accuracy in maintaining documentation and following protocol guidelines.
  • Team Collaboration: Ability to work independently and collaboratively within a multidisciplinary team.
  • Confidentiality: Ability to handle sensitive participant data while adhering to ethical and regulatory guidelines.

Required Experience and Qualifications:

  • Education: Bachelor’s degree preferred.
  • Experience: Previous experience in a healthcare or clinical research setting is a plus.
  • Clinical Trials Knowledge: Previous exposure to clinical trials is preferred but not required.

This role is ideal for someone detail-oriented, organized, and eager to support clinical research in advancing medical knowledge and patient care.