Jobs in the United States

25+ jobs

Save this search

Added just now
Assistant Store Manager (Bilingual)
Community Choice Financial Family of Brands
Las Vegas, NV
…your career by providing an ongoing comprehensive training and development program that will allow you to truly…
Added 1 min ago
TF
Current Department Employees: Staff Nurse - Med/Surg
Tahoe Forest Health System
Truckee, CA
- $70.71 USD / hour
Performs the nursing process through assessment, planning, implementation and evaluation of safe therapeutic care to patients in hospital by performing the following duties.
Added 1 min ago
CH
Registered Nurse or Licensed Practical Nurse- Inpatient
COMPREHENSIVE HEALTHCARE
Selah, WA
- $31.4 to $62.69 USD / hour
Utilizes group process to develop insight, practice skills, and motivate client for change.
Added 1 min ago
Assistant Director, Pre-College and Non-Degree, Slate
George Washington University
DC
…of the student lifecycle, from the admissions and enrollment process through graduation and beyond, by supporting a connected, comprehensive, and student-centered approach to the student…
Added 1 min ago
CO
Program Coordinator
County of San Luis Obispo
San Luis Obispo, CA
- $35.32 to $47.33 USD / hour
A: Possession of an associate’s degree from an accredited college or university. In addition, one year of experience assisting in financial, budgetary, coordination, communication, service…
Added 2 mins ago
A
Animal Care Technician
Actalent
New City, NY
- $20 to $21 USD / hour
Interest in ongoing professional development in animal care and research support, with potential growth into roles such as Research Associate.
Added 2 mins ago
BIM Technician
Actalent
Milwaukee, WI
We are seeking a detail-oriented BIM Technician to support the development, coordination, and maintenance of Building Information Models (BIM) for mechanical, electrical, and plumbing (MEP)…
Added 2 mins ago
Cad Designer
Actalent
Allenton, WI
Participate in new product development and new product introduction (NRE) projects, contributing to design for manufacturability (DFM) implementation.
Added 2 mins ago
UG
Principal Cybersecurity Analyst (Attack Surface Mgt.) On Site MN
UnitedHealth Group
Columbia, MD
- $112,700 to $193,200 USD / year
…We are committed to leveraging every tool, partnership and process needed to enhance our security posture. It is our duty to protect the information of those we serve while Caring.…
Added 2 mins ago
Mechanical Drafter
Actalent
Saint Paul, MN
…manufacturing environment. This role supports both new product development and modifications to existing products, ensuring designs are accurate, manufacturable, and aligned with…
Added 2 mins ago
Controller Associate
IP Global
Springfield, OR · CA
The Controller Associate provides accounting, financial analysis, operational support, and leadership development support within International Paper’s manufacturing finance organization.…
Added 2 mins ago
SO
Special Agent I Cheyenne ICAC 2026-02695
State of Wyoming
WY · Cheyenne, WY
- $45.48 to $50.53 USD / hour
Locate and interview suspects, victims, and other witnesses in the gathering and development of intelligence.
Added 2 mins ago
SO
Special Agent I Rock Springs ICAC 2026-02694
State of Wyoming
WY · Rock Springs, WY
- $45.48 to $50.53 USD / hour
Locate and interview suspects, victims, and other witnesses in the gathering and development of intelligence.
Added 2 mins ago
RN Lead Preceptor - Emergency Care Center - FT Nights
Grady Memorial Hospital Corporation
Atlanta, GA
…pools in their units. The Lead Preceptor will assess new hire development of a defined set of competencies and the achievement of a prescribed set of skills to aid in the new hire…
Added 2 mins ago
CH
Store Associate
CVS Health
Greensboro, NC
- $15 to $18 USD / hour
The Retail Store Associate position provides an opportunity, in a leading retail setting, to excel in a growing, high impact, customer focused role, working both independently and as a…
Added 2 mins ago
CH
Store Associate Seasonal
CVS Health
Marion, NC
- $15 to $18 USD / hour
The Seasonal Retail Store Associate position is a limited-time employment opportunity to support increased summer business and tourism now through Labor Day. Seasonal Store Associates play…
Added 2 mins ago
CH
Store Associate
CVS Health
Zanesville, OH
- $15 USD / hour
The Retail Store Associate position provides an opportunity, in a leading retail setting, to excel in a growing, high impact, customer focused role, working both independently and as a…
Added 2 mins ago
CH
Store Associate
CVS Health
Madisonville, KY
- $15 to $18 USD / hour
The Retail Store Associate position provides an opportunity, in a leading retail setting, to excel in a growing, high impact, customer focused role, working both independently and as a…
Added 2 mins ago
RI
Supply Chain Ops Specialist
Ryder Integrated Logistics, Inc. (Employer-Payroll)
United States
- $50,000 to $59,000 USD / year
Support and aid in the development of system and process training for employees in the work group(s). Perform operational administrative functions to support location activities and / or…
Added 2 mins ago
Senior Ops Manager II
Ryder Truck Rental, Inc. (Employer-Payroll)
United States
…Maintenance Operations policies and procedures. This may also be a development position for Maintenance Manager or Manager of Quality Assurance…
Added 2 mins ago
Operations Supervisor - 2nd Shift 1pm - 9pm
Ryder Truck Rental, Inc. (Employer-Payroll)
United States
…Maintenance Operations policies and procedures. This may also be a development position to prepare incumbents for the Operations Manager…
Added 3 mins ago
Manager, Hedge Fund Accounting
SS&C Technologies, Inc.
United States
…developing your leadership and client management skills. As an Associate Manager, you'll play a key role in delivering exceptional client service, mentoring team members, and driving…
Added 3 mins ago
Senior Associate, Workflow & Automation
WPP Media
NY
The Solutions Group at WPP Media is seeking a Senior Associate, Workflow & Automation to connect technology platforms, operational workflows, and agency teams.
Added 4 mins ago
IT Cloud Engineer, Engineering Platform Automation
Mayo US
Rochester, MN
The engineer will lead the development and continuous evolution of cloud governance automation, engineering request management, ServiceNow Employee Center Pro, EmployeeWorks, knowledge…
Added 5 mins ago
Retail Sales and Store Support
Albertsons Companies
TEMPE, AZ · Tempe, AZ
Leaders invested in your training, career growth & development.

PPD Development, LP

Sr. Clinical Research Associate - Early Phase Studies

Remote, United States

Apply About employer

Applications open in a new tab.

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 Austin, Texas, and candidates must be based in the Austin 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 Austin, TX 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.

Apply About employer

Report this job