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Clinical Drug Screening Associate Jobs in Raleigh, NC

AstraZeneca

Global Study Associate Director

Durham, NC · On-site

Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead ... and clinical/drug development * Demonstrated solid project management skills and knowledge of ...

Astrazeneca

Global Study Associate Director

Durham, NC · On-site

Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead ... and clinical/drug development * Demonstrated solid project management skills and knowledge of ...

AstraZeneca

Global Study Associate Director

Durham, NC · On-site

Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead ... and clinical/drug development * Demonstrated solid project management skills and knowledge of ...

AstraZeneca

Global Study Associate Director

Durham, NC · On-site

Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead ... and clinical/drug development * Demonstrated solid project management skills and knowledge of ...

Automatic Leasing Service

Warehouse Associate

Raleigh, NC · On-site

$20 - $23/hr

Dental insurance Automatic Leasing is hiring a full-time Warehouse Associate to support our ... Must pass a background check and drug screening Benefits: * Full-time position * 401(k) with profit ...

Automatic Leasing Service

Warehouse Associate

Raleigh, NC · On-site

$20 - $23/hr

Dental insurance Automatic Leasing is hiring a full-time Warehouse Associate to support our ... Must pass a background check and drug screening Benefits: * Full-time position * 401(k) with profit ...

Southeastern Tile Connection

Warehouse Associate

Durham, NC · On-site

$14.50 - $17.25/hr

Warehouse Associate Join a Growing Team at Southeastern Tile Connection! Are you dependable ... Ability to pass a pre-employment drug screening and participate in company-required screenings Why ...

Automatic Leasing Service

Warehouse Associate

Raleigh, NC · On-site

$20 - $23/hr

Dental insurance Automatic Leasing is hiring a full-time Warehouse Associate to support our ... Must pass a background check and drug screening Benefits: * Full-time position * 401(k) with profit ...

Mark Jacobson Toyota

Service Porter

Durham, NC · On-site

$14.50 - $17.50/hr

Willing to submit to a pre-employment background check & drug screen Associate Benefits: Full time associates are eligible for medical, dental, vision, and life insurance along with a lease ...

Mark Jacobson Toyota

Service Porter

Durham, NC · On-site

$14.50 - $17.50/hr

Willing to submit to a pre-employment background check & drug screen Associate Benefits: Full time associates are eligible for medical, dental, vision, and life insurance along with a lease ...

Best Tile

Warehouse Associate

Raleigh, NC · On-site

$20 - $22/hr

Best Tile is looking to add an experienced and well-rounded warehouse associate to join our ... drug screening, a physical capacity screening, and background check. These programs balance our ...

Best Tile

Warehouse Associate

Raleigh, NC · On-site

$20 - $22/hr

Best Tile is looking to add an experienced and well-rounded warehouse associate to join our ... drug screening, a physical capacity screening, and background check. These programs balance our ...

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All JobsClinical Drug Screening Associate JobsClinical Drug Screening Associate Jobs in Raleigh, NC

Clinical Drug Screening Associate information

See Raleigh, NC salary details

$12

$30

$53

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

As of Sep 6, 2026, the average hourly pay for clinical drug screening associate in Raleigh, NC is $30.66, according to ZipRecruiter salary data. Most workers in this role earn between $20.58 and $40.43 per hour, depending on experience, location, and employer.

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 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 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.

What are popular job titles related to Clinical Drug Screening Associate jobs in Raleigh, NC?

For Clinical Drug Screening Associate jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Clinical Drug Screening Associate jobs in Raleigh, NC look for?

The top searched job categories for Clinical Drug Screening Associate jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Clinical Drug Screening Associate jobs?

Cities near Raleigh, NC with the most Clinical Drug Screening Associate job openings:

Clinical Drug Screening Associate jobs near you

Senior Clinical Project Manager

Azurity Pharmaceuticals - US

Raleigh, NC • Hybrid

Full-time

Re-posted 3 days ago

Job description

About the Role

The Senior Clinical Project Manager, Clinical Development is responsible for leading the planning, execution, oversight, and delivery of domestic and/or global postmarketing required clinical trials. The Sr. CPM serves as the operational leader for assigned studies, partnering cross-functionally with Medical/Drug Safety, Regulatory, Data Management, Quality, and external vendors to ensure clinical trials are delivered on time, within budget, and in compliance with applicable regulations and quality standards.

 Key Responsibilities

  • Lead the operational execution of assigned domestic or global, multi-center late phase clinical trial(s) including oversight of selected vendor(s)/CRO to ensure accountability, quality, and on time delivery of key project deliverables.
  • Develop and manage study timelines, contract/budget negotiations, and risk mitigation plans to ensure delivery on timeline and financial goals are met.
  • Initiate and manage request for proposal activities for assigned clinical studies or clinical development vendors, including CROs, specialty lab vendors, bioanalytical vendors, etc.
  • Lead study execution team comprised of cross-functional representatives from Regulatory, Drug Safety, Medical, Drug Supply, Data Management, Biostatistics, and Quality to oversee CRO vendors and ensure study excellence.
  • Manage clinical development vendors according to vendor oversight plans.
  • Oversee all study-level data monitoring activities, reviews monitoring visit reports, and conducts Sponsor oversight monitoring visits as required.
  • Responsible for monthly Protocol Deviation (PD) review, including oversight of CRA documentation and collaboration with Medical Monitor for medical review.
  • Prepares and/or reviews study-related study plans/documents; reviews site study documents.
  • Assist in strategic trial design and protocol writing.
  • Strategic country/site selection with program input and ensuring consistency across all clinical projects for therapeutic area.
  • Ensures all clinical trials are executed in compliance with ICH/GCP guidelines/regulations and applicable SOPs: participates in the planning of quality assurance activities and coordinates resolution of audit findings; ensures audit-ready condition of clinical trial documentation including central clinical files, Trial Master File (TMF), and clinical trial registry submissions.
  • Ensure inspection readiness and compliance with ICH-GCP, FDA, EMA, and applicable regulatory requirements.

Required Skills and Experience

  • Bachelor's degree in Life Sciences or a related scientific discipline (advanced degree preferred).
  • 8+ years of Clinical Trial / Project Management experience within CRO, biotechnology or pharmaceutical organizations.
  • Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level.
  • Proven leadership of global clinical studies and cross-functional project teams.
  • Strong experience managing CROs, vendors, and external partners.
  • Extensive knowledge of ICH-GCP, FDA, EMA, and global clinical trial regulations.
  • Excellent communication, leadership, and project management skills.

 Preferred Qualifications

  • 5+ years' experience of clinical trial management for late phase studies
  • Experience with IMP/clinical drug supply logistics, planning, and labeling activities in late phase studies
  • Effective communicator who can manage multiple priorities while building strong internal relationships across multiple departments

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