Jobs in the United States

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Added 4 mins ago
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Supply Chain Product Lifecycle Project Manager, Therapeutic Dermatology
Galderma Laboratories, LP
United States
- $115,000 to $145,000 USD / year
The Associate Director, Omnichannel & Marketing Capabilities, is a senior product and capability leader who serves as the primary bridge between US commercial business needs and technology…
Added 4 mins ago
SO
Quality Assurance Specialist - State Program Administrator Senior
State of Minnesota
St. Paul, MN
- $28.75 to $42.16 USD / hour
…ensuring the accuracy, consistency, and compliance of all claim development activities and determinations. This role is responsible for evaluating claim files, identifying errors or…
Added 4 mins ago
Team Leader Solutions and Data Management
Compeer Financial
Mankato, MN
Our job titles may span more than one career level (associate, senior, principal, etc.). The actual title and base pay offered is dependent upon many factors, such as: training,…
Added 4 mins ago
Senior Treasury Analyst
Blue Cross and Blue Shield of Minnesota
Eagan, MN
The Senior Treasury Analyst will support all aspects of enterprise Treasury activities. This includes but is not limited to strategic treasury recommendations, assessment of capital…
Added 5 mins ago
MC
Development Associate (Hybrid)
Mayo Clinic
Rochester, MN
- $26.63 to $35.98 USD / hour
The Development Associate supports Campaign Administration and Executive & Leadership Engagement through data management, reporting, stakeholder support, process improvement, and…
Added 5 mins ago
Associate Software Engineer
Highmark Health
Saint Paul, MN
…in every aspect as a part of the software application build process from idea generation, business analysis, technical design and software development using the latest technologies and…
Added 5 mins ago
Senior Workday Configurator, Talent
Humana
Saint Paul, MN
The Senior Configuration Professional is a Workday Talent and Performance functional expert who partners with HR, Talent, Performance, Technology, and other business stakeholders to design,…
Added 5 mins ago
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Oracle Fusion Manufacturing Senior Manager - Pharmaceutical
Accenture
Minneapolis, MN
- $122,700 to $302,400 USD / year
As a Senior Manager, you will drive client engagement delivery, mentor consulting teams, support business development activities, and serve as a trusted advisor to executive stakeholders.
Added 5 mins ago
Director Merch Buying - Sport Lifestyle
Target
Minneapolis, MN
…and/or category mangers and vendors will help guide product development as you source appropriately for your category. You will lead Associate Buyers and Senior Merchandise Specialists; and…
Added 5 mins ago
Enterprise Account Project Coordinator III (Remote, USA)
Medtronic
Minneapolis, MN
…meetings, and special projects. The role provides exposure to senior leaders, strategic account planning processes, and cross-functional collaboration across the organization. Less than 10%…
Added 5 mins ago
RU
Name: North American Pursuit Specialist (Government Focus)
RSM US LLP
Minneapolis, MN
- $11.41 USD / hour
This individual supports pursuit material development and quality control activities for assigned complex pursuits, helping ensure materials are accurate, compliant, brand-aligned, and…
Added 5 mins ago
Director Merch Buying, Sports
Target
Minneapolis, MN
…and/or category mangers and vendors will help guide product development as you source appropriately for your category. You will lead Associate Buyers and Senior Merchandise Specialists; and…
Added 8 mins ago
Applications Development Sr Programmer Analyst - AVP
Citibank, N.A.
United States
This role is for a hands-on Applications Development professional responsible for designing, building, and maintaining production-grade Java-based systems within a complex technology…
Added 9 mins ago
Senior Associate, Horizontal HR Business Partner
Capital One
McLean, VA
Complete reporting as a part of key Talent Management/Performance Management/All Associate Survey processes and other key process initiatives
Added 10 mins ago
Solutions Architect AGS-Tech, Early Career - 2027 (US)
Amazon Web Services, Inc. - A97
Austin, TX · Seattle, WA · Arlington, VA
…the afternoon, you might attend a technical session led by a senior SA on emerging technology, then spend time working toward your next AWS certification. Later, you'll collaborate with…
Added 14 mins ago
Business Immigration Associate Attorney - Mandarin Speaking
Fragomen
United States
About the Role: A career as a Business Immigration Associate at Fragomen gives you the opportunity to work with a smart, motivated, and diverse peer group. Our exclusive focus on…
Added 15 mins ago
Applications Development Sr Programmer Analyst - AVP
Citi
TAMPA, FL · Tampa, FL · Tampa
This role is for a hands-on Applications Development professional responsible for designing, building, and maintaining production-grade Java-based systems within a complex technology…
Added 17 mins ago
Associate Director, Price to Win Analyst (Remote)
RTX
Remote, United States
…businesses, world-class operations and investments in research and development, we offer capabilities and opportunity no one else can. Together, we push the boundaries of known science and…
Added 17 mins ago
Associate Strategic Client Executive, Rx Solutions
Marsh McLennan
Raleigh, NC · Golden Valley, MN · Atlanta, GA · Richmond, VA · Greenville, SC · Saddle Brook, NJ · Charlotte, NC · Greensboro, NC · McLean, VA · Dallas, TX
As our Associate Strategic Client Manager on the Rx Solutions team, you’ll serve as the primary contact for field offices, providing support in post-sale implementation and ongoing pharmacy…
Added 21 mins ago
Sr. Talent Acquisition Partner- Manufacturing
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The Senior Talent Acquisition Partner - Manufacturing will play an integral part in providing OneMars full life-cycle, cross segment recruitment expertise on all aspects of the hiring…
Added 26 mins ago
Senior Operations Manager (Operations Manager I)
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Stockbridge, GA
Our Organization has a business casual environment and focuses on teamwork, associate development, training, and continuous improvement.
Added 27 mins ago
Associate Director for Course Support Services
University of North Carolina at Charlotte
NC
The Associate Director for Course Support Services provides strategic leadership, administrative oversight, and vision for all course-based learning assistance programs within the…
Added 27 mins ago
Associate Director, Supply Chain Management
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Rahway, NJ
As the Associate Director, Supply Chain Management, you will lead global design, development, and rollout of demand and supply planning, production planning, and detailed scheduling…
Added 31 mins ago
Investment Banking - Consumer Associate
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New York, NY
We are seeking an Associate to join our Consumer team. The Associate will work directly with senior bankers and play an active role in executing M&A and capital-raising transactions and…
Added 31 mins ago
Recruiter
Veeva
Remote, United States
As a University Recruiter at Veeva, you will be a critical growth driver for our Consultant Development Program (CDP) in North America.

PPD Development, LP

Sr. Clinical Research Associate - Early Phase Studies

Las Vegas, NV, United States

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Job details

Posting language: English
Posted: Nov 6, 2026

Original job description

Work Schedule Standard (Mon-Fri) Environmental Conditions Office

Job Description

Join Us as a Clinical Research Associate – Make an Impact at the Forefront of Innovation

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global Early Development team, you'll have the opportunity to support complex, early-phase clinical trials that advance innovative therapies through critical stages of drug development.

As a Clinical Research Associate (CRA) supporting Early Development studies, you will independently perform and coordinate clinical monitoring and site management activities, with a focus on Phase I and clinical pharmacology studies. You'll conduct remote and on-site visits to assess protocol compliance, participant safety, data integrity, and regulatory adherence.

This position will primarily support an investigational site in Las Vegas, Nevada, and candidates must be based in the Las Vegas area.

While the primary focus will be the Las Vegas site, travel to additional investigational sites in other locations may be required based on business and study needs.

This role requires strong clinical knowledge, independent monitoring expertise, and an understanding of the unique complexities of early-phase research, including intensive safety assessments, dose escalation, pharmacokinetic/pharmacodynamic (PK/PD) sampling, and time-sensitive study procedures.

Acting as a site processes specialist, you will ensure that clinical trials are conducted in accordance with approved protocols, ICH-GCP guidelines, applicable regulations, and standard operating procedures (SOPs), while safeguarding participant rights, safety, and well-being. You will also ensure audit readiness and develop collaborative relationships with investigational sites, sponsors, and cross-functional study teams.

What You'll Do

Independently monitor investigational sites using a risk-based monitoring approach, applying critical thinking, root cause analysis, and problem-solving skills to identify compliance gaps, mitigate risks, and implement corrective and preventive actions.
Conduct site qualification visits, site initiation visits (SIVs), interim monitoring visits (IMVs), and close-out visits (COVs) in accordance with approved monitoring plans, study protocols, and applicable regulatory requirements.
Support Phase I and Early Development studies, including complex clinical pharmacology protocols such as First-in-Human (FIH), Single Ascending Dose (SAD), Multiple Ascending Dose (MAD), and PK/PD studies.
Monitor early-phase study activities with particular attention to participant safety, dose escalation procedures, protocol-defined stopping criteria, dosing requirements, time-sensitive sample collection, and intensive clinical data review.
Perform source data review (SDR), source data verification (SDV), and case report form (CRF) review, as applicable, to ensure data accuracy, completeness, and protocol compliance. Review relevant clinical documentation, including medical histories, laboratory results, concomitant medications, adverse events, and eligibility assessments.
Assess investigational product accountability through physical inventory and records review, ensuring compliance with protocol-specific dosing and administration requirements.
Identify, document, and escalate safety concerns, protocol deviations, data discrepancies, and other study risks in a timely manner. Partner with investigational sites and project teams to ensure appropriate resolution and follow-up.
Document monitoring observations through timely, accurate reports and follow-up letters in accordance with approved business writing standards.
Maintain regular communication with investigational sites between monitoring visits to confirm protocol adherence, resolution of outstanding issues, and timely data entry.
Participate in investigator meetings and collaborate with sponsors and internal teams to support site identification, qualification, initiation, ongoing monitoring, and study close-out activities.
Ensure essential documents are complete, accurate, and maintained in accordance with ICH-GCP, applicable regulations, and project requirements. Conduct on-site file reviews as required.
Maintain accurate and timely study tracking, monitoring documentation, and updates within clinical trial management systems (CTMS) and other applicable platforms.
Facilitate effective communication among investigational sites, sponsors, and cross-functional study teams, particularly regarding time-sensitive clinical activities and emerging study risks.
Support audit and inspection readiness and respond to applicable sponsor, company, and regulatory requirements.
Maintain administrative responsibilities, including expense reports, timesheets, and other required documentation.
Contribute to project initiatives, process improvements, and knowledge sharing across the clinical operations team. May provide guidance or mentoring to less experienced CRAs as appropriate.

Education and Experience Requirements

Bachelor's degree in life sciences, nursing, pharmacy, or a related medical/scientific discipline, or an equivalent combination of education, training, and relevant experience.
3-5+ years of independent clinical monitoring experience as a CRA, including demonstrated experience conducting site qualification, initiation, interim monitoring, and close-out visits.
Previous Phase I / Early Development clinical monitoring experience is strongly preferred, particularly experience supporting complex early-phase or clinical pharmacology studies. Approximately 3+ years of Phase I monitoring experience is ideal; however, candidates with less Phase I experience and substantial hands-on exposure to complex early-phase protocols will also be considered.
Direct monitoring experience with multiple early-phase study designs is highly preferred, particularly First-in-Human (FIH), Single Ascending Dose (SAD), and Multiple Ascending Dose (MAD) studies. Experience with PK/PD, Drug-Drug Interaction (DDI), Food Effect, or Bioavailability/Bioequivalence (BA/BE) studies is also valuable.
Strong medical and scientific knowledge, with demonstrated ability to independently review and interpret clinical source documentation, including medical histories, laboratory results, concomitant medications, adverse events, and eligibility criteria.
Must be based in the Las Vegas, NV area to support the primary investigational site, with flexibility to travel to additional locations as needed.
Valid driver's license where applicable.

An equivalency consisting of a combination of appropriate education, training, and directly related experience may be considered sufficient to meet applicable educational requirements.

Preferred Qualifications

The following experience is highly desirable and may differentiate candidates:

Experience monitoring additional clinical pharmacology studies, including QT/QTc, ADME/mass balance, renal impairment, hepatic impairment, MASH, or other specialty-population studies.
Experience supporting studies involving complex routes of administration, including intravenous (IV), subcutaneous (SC), or other injectable therapies.
Previous monitoring experience within dedicated Phase I units or clinical pharmacology units.
Experience serving as a Lead CRA, mentoring junior CRAs, or assuming additional senior-level monitoring responsibilities.
Experience working independently within lean or cross-functional project structures, including studies without a designated Clinical Trial Manager (CTM).

Knowledge, Skills and Abilities

Strong clinical and medical terminology knowledge, including the ability to review complex clinical data and identify potential safety, eligibility, and protocol compliance concerns.
Thorough understanding of ICH-GCP, applicable regulations, SOPs, and clinical monitoring requirements.
Strong understanding of early-phase clinical trial conduct, including dose escalation, intensive safety monitoring, stopping criteria, dosing procedures, PK/PD sampling requirements, and high-volume source data review.
Demonstrated ability to independently manage monitoring activities, prioritize competing study requirements, and exercise sound clinical judgment.
Well-developed critical thinking, risk assessment, root cause analysis, and problem-solving skills, with the ability to identify and escalate issues appropriately.
Strong understanding of risk-based monitoring concepts and processes.
Excellent written and verbal communication skills, with the ability to collaborate effectively with investigational sites, medical personnel, sponsors, and cross-functional project teams.
Strong interpersonal and relationship management skills, with a customer-focused approach.
Excellent organizational skills, attention to detail, and ability to manage multiple priorities in fast-paced, time-sensitive clinical research environments.
Ability to work independently with minimal oversight while contributing effectively to collaborative study teams.
Flexibility and adaptability to changing study priorities, operational needs, and complex clinical scenarios.
Proficiency in Microsoft Office and the ability to learn and effectively utilize clinical trial management systems and other relevant software.
Strong English language and grammar skills.

Working Conditions and Environment

Location Requirement: Candidates must be based in the Las Vegas, NV area, as this position will primarily support an investigational site in that location.
Travel: Regular travel to the primary Las Vegas investigational site is required, with potential travel to additional sites in other locations based on study assignments and business needs. Overnight travel may be required.
Work is performed in an office, laboratory, clinical, and/or home office environment with exposure to electrical office equipment.
Potential exposure to biological fluids and infectious organisms in clinical environments.
Personal protective equipment, including protective eyewear, garments, and gloves, may be required.
Rare exposure to fluctuating and/or extreme temperatures.

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More about this job

Skills

Clinical research
Clinical trials
Pharmacology
Regulatory compliance
Research
Google Cloud
Critical thinking
Root cause analysis
Problem solving
Documentation
Communication skills
Data entry
Inspection
Coaching
PD
Valid driver's licence
Work independently
Medical terminology
Monitor activities
Hazard assessment
Organizational skills
Attention to detail
Adaptability
Microsoft Office
Office equipment
Personal protective equipment

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