CRA 1, IQVIA Biotech
$71K - $145K/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 ...
$71K - $145K/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 ...
$71K - $145K/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 ...
$71K - $145K/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 ...
$71K - $145K/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 ...
Risk Assessments * Support startup and operational readiness activities for new production ... Experience supporting GMP-regulated pharmaceutical, biotech, medical device, or manufacturing ...
Risk Assessments * Support startup and operational readiness activities for new production ... Experience supporting GMP-regulated pharmaceutical, biotech, medical device, or manufacturing ...
Indianapolis, IN · On-site
... startup experience within pharmaceutical, biotech, or GMP-regulated manufacturing environments • Strong experience supporting large-scale capital projects and facility expansions • Extensive ...
Indianapolis, IN · On-site
... startup experience within pharmaceutical, biotech, or GMP-regulated manufacturing environments • Strong experience supporting large-scale capital projects and facility expansions • Extensive ...
... biotechnology, and life sciences environments. This role will be responsible for ensuring GMP ... Support FAT, SAT, startup, and operational readiness activities. * Manage deviations ...
... biotechnology, and life sciences environments. This role will be responsible for ensuring GMP ... Support FAT, SAT, startup, and operational readiness activities. * Manage deviations ...
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
... 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
Risk Assessments * Support startup and operational readiness activities for new production ... Experience supporting GMP-regulated pharmaceutical, biotech, medical device, or manufacturing ...
Quick apply
Risk Assessments * Support startup and operational readiness activities for new production ... Experience supporting GMP-regulated pharmaceutical, biotech, medical device, or manufacturing ...
Risk Assessments * Support startup and operational readiness activities for new production ... Experience supporting GMP-regulated pharmaceutical, biotech, medical device, or manufacturing ...
Risk Assessments * Support startup and operational readiness activities for new production ... Experience supporting GMP-regulated pharmaceutical, biotech, medical device, or manufacturing ...
... startup. Provide engineering support to strategic site projects, including design reviews ... Experience supporting manufacturing, chemical, pharmaceutical, biotechnology, food processing, or ...
... startup. Provide engineering support to strategic site projects, including design reviews ... Experience supporting manufacturing, chemical, pharmaceutical, biotechnology, food processing, or ...
Lebanon, IN · On-site
$100K - $130K/yr
... startup, loop checks, point-to-point checks, functional testing, and troubleshooting of BMS ... biotech, life sciences, or GMP-regulated manufacturing environments. • Ability to coordinate with ...
Lebanon, IN · On-site
$100K - $130K/yr
... startup, loop checks, point-to-point checks, functional testing, and troubleshooting of BMS ... biotech, life sciences, or GMP-regulated manufacturing environments. • Ability to coordinate with ...
Lafayette, IN · On-site
... and startup activities. • Manage project budgets, schedules, contractors, vendors, and ... biotechnology, food processing, or other regulated industrial operations is beneficial. • ...
Lafayette, IN · On-site
... and startup activities. • Manage project budgets, schedules, contractors, vendors, and ... biotechnology, food processing, or other regulated industrial operations is beneficial. • ...
Indianapolis, IN · On-site
$79K - $105K/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
$79K - $105K/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
$79K - $105K/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
$79K - $105K/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
$79K - $105K/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
$79K - $105K/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 ...
Support commissioning, qualification, startup, and operational readiness activities as needed ... pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
Support commissioning, qualification, startup, and operational readiness activities as needed ... pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
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 ...
Semiconductor, pharmaceutical, or biotech experience a plus. Project Manager with over 10 years of ... system startup as necessary. * Local Candidates Highly Preferred. A relocation package may be ...
Semiconductor, pharmaceutical, or biotech experience a plus. Project Manager with over 10 years of ... system startup as necessary. * Local Candidates Highly Preferred. A relocation package may be ...
Semiconductor, pharmaceutical, or biotech experience a plus. Project Manager with over 10 years of ... system startup as necessary. * Local Candidates Highly Preferred. A relocation package may be ...
Semiconductor, pharmaceutical, or biotech experience a plus. Project Manager with over 10 years of ... system startup as necessary. * Local Candidates Highly Preferred. A relocation package may be ...
Lebanon, IN · On-site
We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity ... Support commissioning, startup, and qualification activities from an HSE perspective. * Investigate ...
Lebanon, IN · On-site
We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity ... Support commissioning, startup, and qualification activities from an HSE perspective. * Investigate ...
A Biotech Startup job involves working in an early-stage company that develops innovative biological or medical technologies. Roles can vary widely, including research, product development, regulatory affairs, and business operations. Employees often wear multiple hats, contributing to both scientific advancements and business growth. The fast-paced environment requires adaptability, problem-solving skills, and a passion for innovation.
To thrive at a biotech startup, you need a strong background in life sciences or bioengineering, paired with an entrepreneurial mindset and practical research experience. Familiarity with laboratory equipment, data analysis software, and, in many cases, regulatory compliance certifications like GLP or GMP are vital. Exceptional adaptability, problem-solving abilities, and teamwork skills are also crucial in this fast-paced, multidisciplinary environment. These competencies help ensure innovation, rapid iteration, and successful navigation of the complex challenges faced by emerging biotech companies.
Working at a biotech startup often means taking on a wide variety of responsibilities, as teams are usually small and roles can be less narrowly defined than at established companies. You may regularly transition between lab research, project management, and business development tasks, which can be both challenging and rewarding. Limited resources, tight deadlines, and the pressure to rapidly produce results are common, but these challenges also provide opportunities for accelerated learning and career advancement. Many employees find the collaborative, innovative atmosphere and the ability to make a tangible impact particularly fulfilling in this setting.

8.1
Based on 53 frontline employees who took The Breakroom Quiz
56th of 210 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 - $145,300.00. 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