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Clinical Research - Medical Assistant

Layton, UT · On-site

$25 - $34/hr

... and biotechnology sponsors is seeking an experienced Clinical Research Coordinator (CRC I) to support clinical trials at our Layton, Utah location. Our research sites conduct Phase II-IV clinical ...

M3USA

Clinical Research Coordinator

Irvine, CA

$30 - $40/hr

Company Description M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology ...

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Biotech Clinical Research information

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$49K

$107.3K

$189K

How much do biotech clinical research jobs pay per year?

As of Jun 14, 2026, the average yearly pay for biotech clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is a Biotech Clinical Research job?

A Biotech Clinical Research job involves conducting and managing clinical trials to evaluate the safety and efficacy of new drugs, medical devices, or treatments developed by biotechnology companies. Professionals in this field ensure compliance with regulatory guidelines, collect and analyze clinical data, and collaborate with cross-functional teams such as scientists, medical professionals, and regulatory authorities. Their work helps bring innovative therapies to market, improving patient care and advancing medical science.

What are the key skills and qualifications needed to thrive in the Biotech Clinical Research position, and why are they important?

To thrive in Biotech Clinical Research, you need a solid background in life sciences, clinical trial methodologies, and regulatory compliance, usually supported by a relevant degree such as biology, biochemistry, or pharmacology. Experience with data management systems, statistical analysis software, and certifications like GCP (Good Clinical Practice) are highly valued. Exceptional attention to detail, effective communication, and strong problem-solving abilities are important soft skills for success in this role. These skills ensure clinical trials are conducted accurately, ethically, and efficiently, supporting the advancement of safe and effective biotech products.

What are some common challenges faced by professionals in biotech clinical research?

Professionals in biotech clinical research often encounter challenges such as managing complex regulatory requirements, adapting to frequent protocol amendments, and coordinating among diverse teams across multiple sites. Ensuring high data quality and maintaining strict timelines can also be demanding, especially as studies progress and new discoveries emerge. However, the dynamic nature of the work offers continuous learning opportunities and the reward of contributing to groundbreaking scientific advancements. Team members typically collaborate closely with clinical monitors, project managers, and regulatory affairs specialists to ensure every aspect of the research process runs smoothly.

More about Biotech Clinical Research jobs
What cities are hiring for Biotech Clinical Research jobs? Cities with the most Biotech Clinical Research job openings:
What are the most commonly searched types of Biotech Clinical Research jobs? The most popular types of Biotech Clinical Research jobs are:
What states have the most Biotech Clinical Research jobs? States with the most job openings for Biotech Clinical Research jobs include:
What job categories do people searching Biotech Clinical Research jobs look for? The top searched job categories for Biotech Clinical Research jobs are:
Biotech Clinical Research jobs near you
Infographic showing various Biotech Clinical Research job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 5% As Needed, 59% Full Time, 23% Part Time, and 12% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.
Clinical Research Associate, IQVIA Biotech

Clinical Research Associate, IQVIA Biotech

IQVIA

Fort Worth, TX

$71K - $169K/yr

Full-time

Posted 28 days ago

IQVIA rating

8.2

Company rating: 8.2 out of 10

Based on 52 frontline employees who took The Breakroom Quiz

46th of 204 rated it services

Job description

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also consider CRA 1 candidates with a minimum of 6 months on-site monitoring experience. 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
We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data.

Key Responsibilities

  • Conduct all types of site visits-selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.

  • Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.

  • Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues.

  • Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.

  • Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries.

  • Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards.

  • Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence.

  • Work closely with cross-functional project teams to support study execution and ensure alignment with project goals.

  • Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking.

Qualifications

  • Bachelor's degree in life sciences or health-related field (or equivalent experience).

  • Requires at least 1 year of on-site monitoring experience.

  • Strong understanding of GCP, ICH guidelines, and regulatory requirements.

  • Ability to travel as required by the project.

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 - $169,300.00. 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.

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About IQVIA

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.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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