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Biotech Case Manager Jobs in Raleigh, NC (NOW HIRING)

IQVIA

Sr. CRA 1, Oncology, IQVIA Biotech

Durham, NC · On-site

$87K - $169K/yr

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and ... enrollment, case report form (CRF) completion and submission, and data query generation and ...

Amgen, Inc.

Staff Relations Manager

Holly Springs, NC · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Track and update cases in the company's case management system. * Assist the Operations Staff ...

Amgen

Staff Relations Manager

Holly Springs, NC

Since 1980,we'vehelped pioneer the world of biotech in our fight against the world's toughest ... Track and update cases in the company's case management system * Assist theOperationsStaff ...

Syngenta Group

Business Operations Lead

Durham, NC · On-site

Financial modeling, data synthesis, business case development. Desired: * Background in biotech ... Change management certification (Prosci, ADKAR). Additional Information Salary for this position ...

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All JobsBiotech Case JobsBiotech Case Manager JobsBiotech Case Manager Jobs in Raleigh, NC

Biotech Case Manager information

See Raleigh, NC salary details

$14

$24

$41

How much do biotech case manager jobs pay per hour?

As of Jul 11, 2026, the average hourly pay for biotech case manager in Raleigh, NC is $24.07, according to ZipRecruiter salary data. Most workers in this role earn between $18.70 and $26.15 per hour, depending on experience, location, and employer.

What is the difference between Biotech Case Manager vs Clinical Research Coordinator?

AspectBiotech Case ManagerClinical Research Coordinator
Required CredentialsHealthcare background, certifications like CCM or case management credentialsResearch-related certifications, clinical trial training
Work EnvironmentBiotech companies, healthcare settings, patient-focusedResearch sites, hospitals, clinical trial environments
Employer & Industry UsageBiotech firms, pharmaceutical companies, healthcare providersAcademic institutions, hospitals, research organizations

Both roles involve patient or participant interaction and require healthcare or research certifications. While a Biotech Case Manager focuses on managing patient cases within biotech or healthcare settings, a Clinical Research Coordinator manages clinical trial processes. They share similar environments but differ in primary responsibilities and certifications.

What are the key skills and qualifications needed to thrive as a Biotech Case Manager, and why are they important?

To thrive as a Biotech Case Manager, you need a solid background in life sciences or healthcare, strong organizational skills, and experience in patient or client management, often supported by a relevant degree. Familiarity with CRM software, electronic health records, and industry-specific platforms is typical, and certifications in case management or healthcare compliance are valuable. Excellent communication, problem-solving abilities, and empathy are the soft skills that help you build relationships and navigate complex cases effectively. These skills and qualities are crucial for ensuring patients receive appropriate care, maintaining regulatory compliance, and optimizing case outcomes in the fast-paced biotech industry.

What is a Biotech Case Manager?

A Biotech Case Manager is a professional who coordinates care and services for patients or clients involved in biotechnology-related treatments, such as gene therapies, biologic drugs, or advanced diagnostics. They serve as a liaison between patients, healthcare providers, insurance companies, and biotech companies to ensure smooth access to complex therapies. Their responsibilities often include patient education, monitoring treatment progress, managing insurance authorizations, and supporting adherence to prescribed therapies. Biotech Case Managers play a critical role in helping patients navigate the unique challenges of advanced biotech treatments, ensuring quality care and positive health outcomes.

What are the main challenges a Biotech Case Manager faces when coordinating care between patients, healthcare providers, and biotech companies?

A Biotech Case Manager often encounters challenges in ensuring seamless communication among patients, healthcare teams, and biotech firms, especially when dealing with complex therapies or clinical trials. Navigating insurance approvals and staying updated on rapidly evolving treatment protocols can also be demanding. Success in this role requires strong organizational skills, adaptability, and the ability to advocate for patients while balancing the interests of multiple stakeholders. Collaboration and clear communication are essential to overcoming these hurdles and providing optimal support to patients.
What are popular job titles related to Biotech Case Manager jobs in Raleigh, NC? For Biotech Case Manager jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Biotech Case Manager jobs in Raleigh, NC look for? The top searched job categories for Biotech Case Manager jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Biotech Case Manager jobs? Cities near Raleigh, NC with the most Biotech Case Manager job openings:
Biotech Case Manager jobs near you
Infographic showing various Biotech Case Manager job openings in Raleigh, NC as of July 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 75% In-person, 8% Hybrid, and 17% Remote job distribution, with an average salary of $50,056 per year, or $24.1 per hour.
Clinical Research Associate, IQVIA Biotech

Clinical Research Associate, IQVIA Biotech

IQVIA, Inc.

Durham, NC • On-site

$71K - $169K/yr

Full-time

Re-posted 25 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

55th of 210 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 at https://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.

What IQVIA employees say

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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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