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Contract Biotech Clinical Research Jobs (NOW HIRING)

IQVIA

Clinical Research Associate, IQVIA Biotech

Houston, TX · On-site

$71K - $169K/yr

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also ... Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play ...

IQVIA

Clinical Research Associate, IQVIA Biotech

Ithaca, NY · On-site

$71K - $169K/yr

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also ... Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play ...

IQVIA

Clinical Research Associate, IQVIA Biotech

Austin, TX · On-site

$71K - $169K/yr

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also ... Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play ...

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Showing results 41-60

All JobsContract Biotech Clinical Research Jobs

Contract Biotech Clinical Research information

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How much do contract biotech clinical research jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for contract biotech clinical research in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

What is the difference between Contract Biotech Clinical Research vs Clinical Research Associate?

AspectContract Biotech Clinical ResearchClinical Research Associate
CredentialsTypically requires a degree in life sciences, certifications like CCR or RAC beneficialRequires a degree in life sciences; certifications like CCR often preferred
Work EnvironmentContract-based, project-specific, often in biotech or pharmaceutical companiesUsually employed by CROs or sponsors, monitoring clinical trials at sites
Employer & IndustryBiotech firms, pharmaceutical companies, contract research organizationsPharmaceutical companies, CROs, biotech firms

Contract Biotech Clinical Research professionals focus on specific projects within biotech or pharma companies, often working on trial design and management. Clinical Research Associates primarily monitor clinical trials at sites, ensuring compliance and data integrity. While both roles require similar credentials and work in related environments, their responsibilities and employment types differ.

What cities are hiring for Contract Biotech Clinical Research jobs? Cities with the most Contract 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 Contract Biotech Clinical Research jobs? States with the most job openings for Contract Biotech Clinical Research jobs include:
Contract Biotech Clinical Research jobs near you

Senior Clinical Research Coordinator

Laborie Medical Technologies Corp

Minnetonka, MN • On-site

$70K - $90K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 24 days ago

Job description

We believe that great healthcare is an essential safeguard of human dignity.
At Laborie, we know the work we do matters - it's what fuels our motivation and contributes to our success. If you're ready to make a positive impact in the lives of patients across the globe, we'd like to meet you.
We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We're not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.
Who We're Looking For:
As a key member of the Clinical team, the Senior Clinical Research Coordinator services as an experienced clinical operations professional responsible for independently managing complex clinical research activities across multiple studies. The Senior CRC provides operational leadership for trial master file (TMF) management, payments, and contract administration while driving process improvements, ensuring inspection readiness, and mentoring less experienced team members. The Senior CRC acts as a key liaison among Clinical, Legal, Finance, Quality, and external stakeholders.
About the Role:
  • Develop and monitor study operational metrics, key performance identifiers, and compliance risks as assigned; collaborate with study teams to mitigate risks.
  • Participate in departmental initiatives to improve operational efficiency and quality.
  • Lead end-to-end TMF strategy and execution for assigned studies.
  • Oversee department payment processes for assigned studies.
  • Monitor payment compliance, forecasting, tracking, and reconciliation activities.
  • Lead and manage administration and timelines, proactively identify and mitigate delays, and ensure timely execution of clinical, vendor/CRO service, consultant, and related agreements.
  • Coordinate and support study- and department-related meetings, including developing agendas, preparing materials, and documenting and distributing meeting minutes.

Minimum Qualifications:
  • Bachelor's degree in Life Sciences, Health Sciences, Business Administration, or a related field, or equivalent combination of education and experience.
  • 4-6 years of clinical research, clinical operations, TMF management, contract administration, or related experience; medical device, pharmaceutical, or biotechnology industry experience preferred.
  • Experience independently managing clinical study documentation and operational processes.
  • Demonstrated ability to lead complex operational activities with minimal supervision.
  • Strong knowledge of ICH-GCP, TMF requirements, and clinical research regulations.
  • Proficiency with eTMF systems, contract tracking tools, and Microsoft Office applications.
  • Advanced understanding of clinical trial documentation, contracts, and payment processes.
  • Excellent organizational, communication, and stakeholder management skills with strong analytical and problem-solving skills.
  • Ability to identify risks, influence outcomes, and drive process improvements.

Why Laborie:
Our Mission every day is to operate as a world-class specialist medical company making and advancing technologies that preserve and restore human dignity. We do that today by helping people with pelvic and gastrointestinal conditions live normal lives, and by helping mothers and babies have safe deliveries.
  • Paid time off and paid volunteer time
  • Medical, Dental, Vision and Flexible Spending Account
  • Health Savings Account with Company Funded Contributions
  • 401k Retirement Plan with Company Match
  • Parental Leave and Adoption Services
  • Health and Wellness Programs and Events
  • Awarded 2025 Cigna Healthy Workforce Designation Gold Level

Laborie provides equal employment opportunities and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation, or any characteristic protected under applicable law. Laborie is committed to providing access and reasonable accommodation in our services, activities, education, and employment for individuals with disabilities.

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