CRA 1, IQVIA Biotech
$71.90K - $119.90K/yr
IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...
$71.90K - $119.90K/yr
IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...
$71.90K - $119.90K/yr
IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...
$71.90K - $119.90K/yr
IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...
$71.90K - $119.90K/yr
IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...
Must be willing to accept significant learning challenges inherent in a first-in-class biotechnology startup * Excellent organizational and time management skills and the ability to prioritize work ...
Must be willing to accept significant learning challenges inherent in a first-in-class biotechnology startup * Excellent organizational and time management skills and the ability to prioritize work ...
Must be willing to accept significant learning challenges inherent in a first-in-class biotechnology startup * Excellent organizational and time management skills and the ability to prioritize work ...
Quick apply
... startup teams Core Requirements: 15+ years in E&I construction leadership Strong QA / quality oversight experience Turnover / commissioning readiness experience Pharma / biotech / food / medical ...
... startup teams Core Requirements: 15+ years in E&I construction leadership Strong QA / quality oversight experience Turnover / commissioning readiness experience Pharma / biotech / food / medical ...
Manage work orders and documentation in CMMS * Assist with equipment startup, commissioning ... Pharma, biotech, or medical device background preferred
Quick apply
Manage work orders and documentation in CMMS * Assist with equipment startup, commissioning ... Pharma, biotech, or medical device background preferred
Be Seen First
Support startup, operational readiness, and technology transfer activities. * Present project ... Minimum 8-12 years of experience in pharmaceutical, biotech, or life sciences industries. * Minimum ...
New
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Be Seen First
Support startup, operational readiness, and technology transfer activities. * Present project ... Minimum 8-12 years of experience in pharmaceutical, biotech, or life sciences industries. * Minimum ...
New
... with equipment installation, startup, commissioning, and validation activities * Support ... Prior experience in pharmaceutical, biotechnology, or medical device industries preferred
Quick apply
... with equipment installation, startup, commissioning, and validation activities * Support ... Prior experience in pharmaceutical, biotechnology, or medical device industries preferred
$79.80K - $105.60K/yr
What You Will Do * Provide on-site startup, commissioning, and troubleshooting support for ... Life sciences, pharmaceutical, biotech, or other GMP-regulated industries * Exposure to Industry 4 ...
$79.80K - $105.60K/yr
What You Will Do * Provide on-site startup, commissioning, and troubleshooting support for ... Life sciences, pharmaceutical, biotech, or other GMP-regulated industries * Exposure to Industry 4 ...
Lebanon, IN · On-site
Design and develop BMS and automation solutions for GMP/GxP-regulated pharmaceutical, biotech, and ... Lead commissioning, startup, and qualification activities for BMS and automation systems. * Execute ...
Lebanon, IN · On-site
Design and develop BMS and automation solutions for GMP/GxP-regulated pharmaceutical, biotech, and ... Lead commissioning, startup, and qualification activities for BMS and automation systems. * Execute ...
This is a unique opportunity to be a part of the team for the startup of a greenfield manufacturing ... Knowledge of cell culture, purification and the support systems used in the manufacture of biotech ...
This is a unique opportunity to be a part of the team for the startup of a greenfield manufacturing ... Knowledge of cell culture, purification and the support systems used in the manufacture of biotech ...
This is a unique opportunity to be a part of the team for the startup of a greenfield manufacturing ... Knowledge of cell culture, purification and the support systems used in the manufacture of biotech ...
This is a unique opportunity to be a part of the team for the startup of a greenfield manufacturing ... Knowledge of cell culture, purification and the support systems used in the manufacture of biotech ...
This is a unique opportunity to be a part of the startup team for a greenfield manufacturing site ... Master's degree with 5+ years of relevant experience in a pharmaceutical or biotechnology ...
This is a unique opportunity to be a part of the startup team for a greenfield manufacturing site ... Master's degree with 5+ years of relevant experience in a pharmaceutical or biotechnology ...
This is a unique opportunity to be a part of the startup team for a greenfield manufacturing site ... Master's degree with 5+ years of relevant experience in a pharmaceutical or biotechnology ...
This is a unique opportunity to be a part of the startup team for a greenfield manufacturing site ... Master's degree with 5+ years of relevant experience in a pharmaceutical or biotechnology ...
Indianapolis, IN · On-site
$79.80K - $105.60K/yr
Provide on-site startup and commissioning support for industrial automation systems * Troubleshoot ... Life sciences, pharmaceutical, biotech, or other regulated manufacturing * Industry 4.0 or Unified ...
Indianapolis, IN · On-site
$79.80K - $105.60K/yr
Provide on-site startup and commissioning support for industrial automation systems * Troubleshoot ... Life sciences, pharmaceutical, biotech, or other regulated manufacturing * Industry 4.0 or Unified ...
Indianapolis, IN · On-site
$79.80K - $105.60K/yr
Provide on-site startup and commissioning support for industrial automation systems * Troubleshoot ... Life sciences, pharmaceutical, biotech, or other regulated manufacturing * Industry 4.0 or Unified ...
Quick apply
Indianapolis, IN · On-site
$79.80K - $105.60K/yr
Provide on-site startup and commissioning support for industrial automation systems * Troubleshoot ... Life sciences, pharmaceutical, biotech, or other regulated manufacturing * Industry 4.0 or Unified ...
$50 - $70/hr
Background in GMP / regulated environments (pharma, biotech, food, etc.) * Someone who understands ... a startup manufacturing environment. About us...Sterling Engineering, in business for 57 years ...
Quick apply
$50 - $70/hr
Background in GMP / regulated environments (pharma, biotech, food, etc.) * Someone who understands ... a startup manufacturing environment. About us...Sterling Engineering, in business for 57 years ...
Indianapolis, IN · Remote
$180K - $230K/yr
Experience building teams in startup or pre-launch biotech environments 【For NYC】Compensation Description (annually): Please note that the base salary range is a guideline, and individual total ...
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Indianapolis, IN · Remote
$180K - $230K/yr
Experience building teams in startup or pre-launch biotech environments 【For NYC】Compensation Description (annually): Please note that the base salary range is a guideline, and individual total ...
Noblesville, IN · On-site
$40 - $45/hr
... installation, startup, and commissioning activities • Participate in SAT, IQ/OQ, and PQ ... biotech, or regulated manufacturing environments Experience with equipment commissioning or ...
Quick apply
Noblesville, IN · On-site
$40 - $45/hr
... installation, startup, and commissioning activities • Participate in SAT, IQ/OQ, and PQ ... biotech, or regulated manufacturing environments Experience with equipment commissioning or ...
In the project delivery phase and startup phase of the project (startup expected 2025 to 2027 ... Experience running projects in pharmaceutical/biotechnology industry, preferably in an API pilot ...
In the project delivery phase and startup phase of the project (startup expected 2025 to 2027 ... Experience running projects in pharmaceutical/biotechnology industry, preferably in an API pilot ...
$22K - $38.9K
9% of jobs
$49.3K is the 25th percentile. Wages below this are outliers.
$38.9K - $55.8K
25% of jobs
$55.8K - $72.7K
14% of jobs
The median wage is $73.9K / yr.
$72.7K - $89.5K
21% of jobs
$99.4K is the 75th percentile. Wages above this are outliers.
$89.5K - $106.4K
9% of jobs
$106.4K - $123.3K
5% of jobs
$123.3K - $140.1K
3% of jobs
$140.1K - $157K
3% of jobs
$157K - $173.9K
2% of jobs
$173.9K - $190.8K
3% of jobs
$190.8K - $207.6K
4% of jobs
$22K
$89.1K
$207.6K
8.1
Based on 51 frontline employees who took The Breakroom Quiz
54th of 203 rated it services
IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have experience monitoring in oncology solid tumor.
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.
Job Overview
The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities. In this position, you will ensure that assigned study sites conduct trials in compliance with the protocol, applicable regulations, Good Clinical Practice (GCP), and ICH guidelines. This role is essential in protecting patient safety, ensuring highquality clinical data, and maintaining study integrity.
Key Responsibilities
As a CRA I, you will conduct various types of monitoring visits-including site selection, initiation, routine monitoring, and closeout visits-to evaluate the quality and integrity of site practices. You will verify that study activities are performed according to regulatory requirements and sponsor expectations, escalating quality concerns as necessary. During these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the Trial Master File (TMF) and the Investigator Site File (ISF).
A central part of this role involves building and maintaining strong communication with investigative sites. You will provide protocol training, set expectations, address sitelevel challenges, and support recruitment planning to help sites meet enrollment targets. You will also collaborate closely with internal project teams to ensure cohesive study execution and may contribute to site-level financial processes or startup activities based on study needs.
Accurate and timely documentation is critical. The CRA I prepare detailed monitoring visit reports, followup letters, and all required study documentation to ensure audit readiness and transparent oversight. The ability to manage multiple tasks, prioritize effectively, and work independently while maintaining productive team relationships is essential for success.
Qualifications
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $71,900.00 - $119,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.Sourced by ZipRecruiter
At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.
Health care and social assistance
10,000+ Employees
Durham, NC, US