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Biotech Cro Jobs (NOW HIRING)

Legend Biotech USA, Inc.

Advanced degree preferred.7+ years of pharmaceutical, biotech, CRO, or related clinical research experience; 10+ years preferred.Experience working with data sources to inform trial forecast ...

Legend Biotech USA, Inc.

$127K - $167K/yr

Advanced degree preferred.7+ years of pharmaceutical, biotech, CRO, or related clinical research experience.Strong experience in vendor oversight, outsourcing, site contracts, investigator payments ...

Legend Biotech USA, Inc.

Advanced degree preferred.7+ years of pharmaceutical, biotech, CRO, or related clinical research experience.Experience in clinical operations with exposure to sample management, lab operations, or ...

Gator Bio

VP of Global Sales

Palo Alto, CA · On-site

Gator Bio's customers include pharma, biopharma, biotech, CRO's, CDMO's, and academic research labs. We sell to North America, APAC, and Europe. We are looking for an experienced executive, well ...

Gator Bio

VP of Global Sales

Palo Alto, CA · On-site

$250K - $280K/yr

Gator Bio's customers include pharma, biopharma, biotech, CRO's, CDMO's, and academic research labs. We sell to North America, APAC, and Europe. We are looking for an experienced executive, well ...

Gator Bio

VP of Global Sales

Palo Alto, CA

Gator Bio's customers include pharma, biopharma, biotech, CRO's, CDMO's, and academic research labs. We sell to North America, APAC, and Europe. We are looking for an experienced executive, well ...

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$25

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How much do biotech cro jobs pay per hour?

As of Jul 21, 2026, the average hourly pay for biotech cro in the United States is $54.35, according to ZipRecruiter salary data. Most workers in this role earn between $39.90 and $64.18 per hour, depending on experience, location, and employer.

What is the highest paying job in biotech?

In biotech, senior executive roles such as Chief Scientific Officer (CSO) or Vice President of Research typically have the highest salaries, often exceeding $200,000 annually. These positions require extensive experience, advanced degrees, and leadership skills, and they oversee research strategies and company direction.

Is it better to work for a CRO or pharmaceutical company?

A Biotech CRO (Contract Research Organization) offers opportunities to work on diverse clinical trials and gain experience in research services, often with flexible project-based roles. Pharmaceutical companies typically provide more stable employment, larger teams, and focus on drug development and manufacturing. The choice depends on career goals, preferred work environment, and desired skill development.

Is IQVIA biotech a CRO?

IQVIA is a global provider of advanced analytics, technology solutions, and contract research services, making it a Contract Research Organization (CRO). As a biotech-focused CRO, IQVIA supports clinical trials, data management, and regulatory consulting for biotech companies. Job roles within IQVIA often require knowledge of clinical research processes and regulatory standards.

What does a CRO do in biotech?

A CRO, or Contract Research Organization, in biotech provides outsourced research services to support drug development, including clinical trial management, regulatory compliance, and data analysis. They help biotech companies conduct studies efficiently and meet regulatory standards using specialized expertise and tools.
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Biotech Cro jobs near you
Infographic showing various Biotech Cro job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 90% Full Time, 1% Part Time, 1% Temporary, and 6% Contract. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $113,048 per year, or $54.4 per hour.

Manager, Site Contracts & Payments Management

Legend Biotech US

Somerset, NJ • Hybrid

$94K - $125K/yr

Other

Re-posted 14 days ago

Job description

Legend Biotech is seeking a Manager, Site Contracts & Payments Management as part of the Clinical Operations team based in Somerset, NJ.

Role Overview

The Site Contracts & Payments Manager is responsible for site contracting and investigator payment process oversight and management, and vendor due diligence across Legend pipeline studies. The role serves as a central point of accountability for improving operational effectiveness, financial discipline, and sponsor-CRO-site workflow alignment for site contracting and payment processes.

Key Responsibilities

  • Partner with CROs to develop and oversee process workflows, and create visibility into site contract and investigator payment workflow efficiency across studies.
  • Partner with CROs, AP, Procurement, Finance, Legal, and study teams to align process workflows, identify gaps, and improve efficiency in contracting and payment execution.
  • Monitor key milestones, bottlenecks, and escalations affecting site startup experience for contracting, payment timeliness, and financial predictability.
  • Support reconciliation, issue resolution, and continuous improvement related to site contracting and investigator payment operations.
  • Coordinate vendor due diligence and risk assessment activities with Procurement, Finance, QA, and other stakeholders.
  • Performs other duties as required.

Requirements

  • Minimum degree requirements of a bachelor's degree (BA, BS) in scientific, health care, business, or related discipline. Advanced degree preferred.
  • 7+ years of pharmaceutical, biotech, CRO, or related clinical research experience.
  • Strong experience in vendor oversight, outsourcing, site contracts, investigator payments, or related operational functions required.
  • Experience working cross-functionally with AP, Procurement, Finance, and Legal required.
  • Experience working in SAP/4 Hanna preferred.
  • Experience establishing KPIs and oversight models preferred.
  • Oncology, cell therapy, or early-phase clinical operations experience preferred.
  • Ability to travel as necessary (up to 10%).
  • Effective oral, written, and interpersonal communication skills.
  • Strong process management, organizational, and problem-solving skills.
  • Ability to identify operational risk and drive practical mitigation strategies.
  • Strong project management skills and the ability to manage multiple priorities.
  • Computer literacy required (MS Word, MS Excel, MS PowerPoint, MS Project).
  • Working knowledge of GCP, FDA, and ICH Guidelines.

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