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Program Biotech Jobs in Raleigh, NC (NOW HIRING)

Senior Electrical Engineer

Cary, NC · On-site

$99K - $129K/yr

Work directly with lead engineers to design electrical systems for Biotech and Pharmaceutical ... Project and Program Management, Procurement, Design, Construction Management, Health and Safety ...

Senior Electrical Engineer

Cary, NC · On-site

$99K - $129K/yr

Work directly with lead engineers to design electrical systems for Biotech and Pharmaceutical ... Project and Program Management, Procurement, Design, Construction Management, Health and Safety ...

... biotech, semiconductor, or high‑purity industries preferred. * Proficiency with orbital welding systems and basic welding program adjustments. * Strong understanding of ASME BPE standards, sanitary ...

Our lead programs, gene therapies for X-linked retinoschisis (XLRS) and GUCY2D - Leber congenital ... biotech environment while supporting Atsenas pipeline across the product lifecycle. Key ...

... biotech, medical device, or food manufacturing). * Strong knowledge of HVAC systems, controls, and preventive maintenance programs. * Ability to read technical manuals, blueprints, and schematics.

... for Biotech and Pharmaceutical and Semiconductor clients. The Senior Mechanical Designer is ... Project and Program Management, Procurement, Design, Construction Management, Health and Safety ...

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Showing results 1-20

Program Biotech information

See Raleigh, NC salary details

$24.3K

$50.9K

$88K

How much do program biotech jobs pay per year?

As of Jun 18, 2026, the average yearly pay for program biotech in Raleigh, NC is $50,898.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,900.00 and $57,800.00 per year, depending on experience, location, and employer.

What is a Program Biotech?

A Program Biotech is a professional who manages and coordinates biotechnology projects or programs within an organization. They oversee research and development activities, ensure compliance with regulations, manage budgets, and facilitate collaboration between scientists, engineers, and other stakeholders. Their role is crucial in bringing biotech innovations from concept to market by ensuring projects stay on schedule and meet organizational goals.

What is the difference between Program Biotech vs Laboratory Technician?

AspectProgram BiotechLaboratory Technician
Required CredentialsBiotech degree or certification, specialized trainingAssociate degree or certification in laboratory sciences
Work EnvironmentResearch labs, biotech companies, pharmaceutical firmsClinical, research, or industrial labs
Employer & Industry UsageBiotech firms, research institutions, pharma companiesHospitals, research labs, manufacturing plants
Common Search & ComparisonYesNo

Program Biotech professionals focus on research, development, and overseeing biotech projects, often requiring advanced degrees and specialized training. Laboratory Technicians perform routine lab tests and support research or manufacturing processes, typically with an associate degree. While both roles work in lab environments within the biotech and healthcare industries, Program Biotech roles are more research-oriented, whereas Laboratory Technicians handle day-to-day testing and sample analysis.

What are some common challenges faced by Program Biotech professionals when managing cross-functional teams?

Program Biotech professionals often coordinate projects that involve diverse teams, including research scientists, regulatory specialists, and business development staff. One key challenge is ensuring clear communication and alignment among team members with varying backgrounds and priorities. Additionally, balancing project timelines with regulatory requirements and scientific uncertainties can require strong problem-solving skills. Being proactive in facilitating collaboration and adapting to shifting project goals are essential for success in this role.

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

To excel as a Program Biotech professional, you need a solid background in life sciences, project management, and regulatory knowledge, often supported by an advanced degree in biotechnology or a related field. Familiarity with laboratory information management systems (LIMS), project management software, and compliance frameworks like GLP or GMP is common. Strong leadership, problem-solving abilities, and effective communication are crucial soft skills for coordinating multidisciplinary teams. These skills and qualifications are essential to drive innovation, ensure regulatory compliance, and achieve successful outcomes in complex biotech projects.
What job categories do people searching Program Biotech jobs in Raleigh, NC look for? The top searched job categories for Program Biotech jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Program Biotech jobs? Cities near Raleigh, NC with the most Program Biotech job openings:
Associate Clinical Project Manager, Immuno-Oncology, Cell and Gene Therapy, IQVIA Biotech

Associate Clinical Project Manager, Immuno-Oncology, Cell and Gene Therapy, IQVIA Biotech

IQVIA

Durham, NC • On-site

$68K - $171K/yr

Full-time

Posted 7 days ago


IQVIA rating

8.2

Company rating: 8.2 out of 10

Based on 52 frontline employees who took The Breakroom Quiz

45th of 204 rated it services


Job description

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.

As an Associate Project Manager (APM), you'll play a critical role in delivering clinical trials that bring innovative therapies to patients faster. You'll support project leadership, collaborate across teams, and help ensure studies are executed on time, on budget, and at the highest quality standards. This role offers strong growth potential, including opportunities to lead smaller studies.

Overview

  • Support delivery of clinical trials across Immuno-Oncology and Cell & Gene Therapy programs

  • Contribute to study plans and oversee assigned study components

  • Coordinate cross-functional teams to meet timelines and milestones

  • Monitor study progress, identify risks, and drive solutions

  • Ensure compliance with protocols, SOPs, and regulatory requirements (ICH-GCP)

  • Support project financials, forecasting, and scope management

  • Communicate updates to internal teams and clients

  • Lead sub-teams or vendors, as needed

Qualifications:

  • Bachelor's degree in life sciences or related field

  • ~2+ years of clinical research experience

  • Understanding of clinical trial processes and regulations (ICH-GCP)

  • Strong project coordination, organization, and problem-solving skills

  • Excellent communication and stakeholder management abilities

  • Ability to manage multiple priorities in a fast-paced environment

  • Proficiency with MS Office tools

Preferred Experience

  • Cell & Gene Therapy, including CAR-T and cellular therapies

  • Immunotherapy

  • Global project management

  • Study start-up & initiation and study close-out

  • First-in-human trials

  • Dose escalation and dose expansion studies

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 $68,400.00 - $171,000.00. 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

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


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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