CRA 1, IQVIA Biotech
$71K - $119K/yr
The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...
CRA 1, IQVIA Biotech
$71K - $119K/yr
The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...
Construction Manager
Richmond, VA · On-site
Extensive experience managing cleanroom or controlled‑environment projects in semiconductor, biotech, pharma, aerospace, or advanced manufacturing * Strong understanding of cleanroom ...
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Construction Manager
Richmond, VA · On-site
Extensive experience managing cleanroom or controlled‑environment projects in semiconductor, biotech, pharma, aerospace, or advanced manufacturing * Strong understanding of cleanroom ...
... management, preferably in a pharmaceutical, cosmetics, biotech, or food manufacturing environment. * Experience managing capital projects and working in a cGMP-regulated facility preferred. Skills ...
... management, preferably in a pharmaceutical, cosmetics, biotech, or food manufacturing environment. * Experience managing capital projects and working in a cGMP-regulated facility preferred. Skills ...
Dynalectric Company
$100K - $125K/yr
... biotech, healthcare, commercial, transportation, and technology companies, as well as many ... Execute and manage all terms of project contracts. * Partner with Foreman, Project Engineers ...
Dynalectric Company
$100K - $125K/yr
... biotech, healthcare, commercial, transportation, and technology companies, as well as many ... Execute and manage all terms of project contracts. * Partner with Foreman, Project Engineers ...
Project Officer
Abingdon, VA · Hybrid
... and biotechnology companies Key responsibilities will include :- * Reviewing new contracts for ... Manage project completion and keep project information up to date * Deal with customer queries ...
Project Officer
Abingdon, VA · Hybrid
... and biotechnology companies Key responsibilities will include :- * Reviewing new contracts for ... Manage project completion and keep project information up to date * Deal with customer queries ...
Project Officer
Abingdon, VA · Hybrid
... and biotechnology companies Key responsibilities will include :- * Reviewing new contracts for ... Manage project completion and keep project information up to date * Deal with customer queries ...
Project Officer
Abingdon, VA · Hybrid
... and biotechnology companies Key responsibilities will include :- * Reviewing new contracts for ... Manage project completion and keep project information up to date * Deal with customer queries ...
... special projects, course needs, etc.), manage the onsite facilities and associated equipment ... Minimum three years of experience in the biotech industry. Preferred Qualifications: Demonstrated ...
... special projects, course needs, etc.), manage the onsite facilities and associated equipment ... Minimum three years of experience in the biotech industry. Preferred Qualifications: Demonstrated ...
Excellent project management skills. * Hands-on approach, with a 'can do' attitude. * Ability to ... Bachelor's Degree in Chemistry, Biochemistry, or Biotechnology related scientific discipline with ...
Excellent project management skills. * Hands-on approach, with a 'can do' attitude. * Ability to ... Bachelor's Degree in Chemistry, Biochemistry, or Biotechnology related scientific discipline with ...
Sr. Validation Manager
Petersburg, VA · On-site
Experience * 8+ years of experience in pharmaceutical/biotech manufacturing. * 5+ years in CQV ... Project Management * Risk-Based Thinking * Cross-Functional Collaboration * Problem Solving ...
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Sr. Validation Manager
Petersburg, VA · On-site
Experience * 8+ years of experience in pharmaceutical/biotech manufacturing. * 5+ years in CQV ... Project Management * Risk-Based Thinking * Cross-Functional Collaboration * Problem Solving ...
Sr. Validation Manager
Petersburg, VA · On-site
Experience * 8+ years of experience in pharmaceutical/biotech manufacturing. * 5+ years in CQV ... Project Management * Risk-Based Thinking * Cross-Functional Collaboration * Problem Solving ...
Sr. Validation Manager
Petersburg, VA · On-site
Experience * 8+ years of experience in pharmaceutical/biotech manufacturing. * 5+ years in CQV ... Project Management * Risk-Based Thinking * Cross-Functional Collaboration * Problem Solving ...
Experience * 8+ years of experience in pharmaceutical/biotech manufacturing. * 5+ years in CQV ... Project Management * Risk-Based Thinking * Cross-Functional Collaboration * Problem Solving ...
Experience * 8+ years of experience in pharmaceutical/biotech manufacturing. * 5+ years in CQV ... Project Management * Risk-Based Thinking * Cross-Functional Collaboration * Problem Solving ...
Experience * 8+ years of experience in pharmaceutical/biotech manufacturing. * 5+ years in CQV ... Project Management * Risk-Based Thinking * Cross-Functional Collaboration * Problem Solving ...
Experience * 8+ years of experience in pharmaceutical/biotech manufacturing. * 5+ years in CQV ... Project Management * Risk-Based Thinking * Cross-Functional Collaboration * Problem Solving ...
Finance Manager
Charlottesville, VA · Hybrid
Evestia Clinical is a biotech-focused global CRO delivering authentic expertise and personalized ... Coordinate with Project Management and Business Development teams to track project profitability ...
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Finance Manager
Charlottesville, VA · Hybrid
Evestia Clinical is a biotech-focused global CRO delivering authentic expertise and personalized ... Coordinate with Project Management and Business Development teams to track project profitability ...
Senior Program Manager, Product Development
$110K - $150K/yr
Extensive knowledge of formal project management methodologies and proven experience applying them within the Biotechnology, Clinical Laboratory, or Medical Device industries. * Regulatory ...
Senior Program Manager, Product Development
$110K - $150K/yr
Extensive knowledge of formal project management methodologies and proven experience applying them within the Biotechnology, Clinical Laboratory, or Medical Device industries. * Regulatory ...
Guidehouse's Life Sciences practice is an engine of innovation, helping pharmaceutical, biotech ... Managing Consultants are responsible for managing projects from cultivation to completion. In this ...
Guidehouse's Life Sciences practice is an engine of innovation, helping pharmaceutical, biotech ... Managing Consultants are responsible for managing projects from cultivation to completion. In this ...
... biotech and pharmaceutical companies. Manage the entire sales pipeline, including in territory ... to Project Management post-award. Manage selected accounts to encourage repeat business and ...
... biotech and pharmaceutical companies. Manage the entire sales pipeline, including in territory ... to Project Management post-award. Manage selected accounts to encourage repeat business and ...
... biotech and pharmaceutical companies. Manage the entire sales pipeline, including in territory ... to Project Management post-award. Manage selected accounts to encourage repeat business and ...
... biotech and pharmaceutical companies. Manage the entire sales pipeline, including in territory ... to Project Management post-award. Manage selected accounts to encourage repeat business and ...
... biotech and pharmaceutical companies. Manage the entire sales pipeline, including in territory ... to Project Management post-award. Manage selected accounts to encourage repeat business and ...
... biotech and pharmaceutical companies. Manage the entire sales pipeline, including in territory ... to Project Management post-award. Manage selected accounts to encourage repeat business and ...
Bachelor's Degree or above in Microbiology or Biotechnology related scientific discipline ... Excellent project management skills. * Hands-on approach, with a 'can do' attitude. * Ability to ...
Bachelor's Degree or above in Microbiology or Biotechnology related scientific discipline ... Excellent project management skills. * Hands-on approach, with a 'can do' attitude. * Ability to ...
Senior Financial Manager
Arlington, VA · On-site
$105K - $165K/yr
... biotechnology, and space control market spaces. Qualified candidates will be part of an exceptional ... Perform as project liaison and provide statistical analysis experience. * Manage stakeholder ...
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Senior Financial Manager
Arlington, VA · On-site
$105K - $165K/yr
... biotechnology, and space control market spaces. Qualified candidates will be part of an exceptional ... Perform as project liaison and provide statistical analysis experience. * Manage stakeholder ...
Project Manager Biotech information
See Virginia salary details
$21.69 - $26.61
4% of jobs
$26.61 - $31.52
8% of jobs
$31.52 - $36.44
3% of jobs
$38.59 is the 25th percentile. Wages below this are outliers.
$36.44 - $41.36
21% of jobs
The median wage is $44.43 / hr.
$41.36 - $46.28
21% of jobs
$49.61 is the 75th percentile. Wages above this are outliers.
$46.28 - $51.20
25% of jobs
$51.20 - $56.11
13% of jobs
$56.11 - $61.03
2% of jobs
$61.03 - $65.95
1% of jobs
$65.95 - $70.87
1% of jobs
$70.87 - $75.79
0% of jobs
$21
$45
$75
How much do project manager biotech jobs pay per hour?
As of Jun 9, 2026, the average hourly pay for project manager biotech in Virginia is $45.85, according to ZipRecruiter salary data. Most workers in this role earn between $39.81 and $50.29 per hour, depending on experience, location, and employer.
What is the difference between Project Manager Biotech vs Clinical Project Manager?
| Aspect | Project Manager Biotech | Clinical Project Manager |
|---|---|---|
| Credentials | Bachelor's or Master's in Life Sciences, Project Management Certification | Bachelor's or Master's in Life Sciences, Clinical Research Certification |
| Work Environment | Biotech companies, R&D labs, manufacturing | Clinical trial sites, hospitals, pharmaceutical companies |
| Industry Usage | Biotech product development, research projects | Clinical trial management, regulatory compliance |
| Common Search/Comparison | Yes | Yes |
The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.
How does a Project Manager in biotech typically collaborate with cross-functional teams to drive project success?
A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.
What does a Project Manager in Biotech do?
A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.
What are the key skills and qualifications needed to thrive as a Project Manager in Biotech, and why are they important?
To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.
What are popular job titles related to Project Manager Biotech jobs in Virginia? For Project Manager Biotech jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Project Manager Biotech jobs in Virginia look for? The top searched job categories for Project Manager Biotech jobs in Virginia are:
What cities in Virginia are hiring for Project Manager Biotech jobs? Cities in Virginia with the most Project Manager Biotech job openings:
IQVIA rating
8.1
Based on 51 frontline employees who took The Breakroom Quiz
53rd of 203 rated it services
Job description
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
- Bachelor's degree required; a scientific or healthcare discipline is preferred.
- 6 months -2 years of relevant experience, with equivalent combinations of education, training, or completion of a CRA training program considered.
- Basic knowledge of clinical research regulations (GCP/ICH).
- 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 - $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.
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