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Director Biotech Clinical Research Jobs (NOW HIRING)

NY · On-site

$90 - $100/hr

Senior Clinical Research Coordinator (CRC) Full time | Smarter HR Solutions LLC | United States Posted On 07/27/2026 Job Information Pharma/Biotech/Clinical Research Work Experience 4-5 years $90,000 ...

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

As of Aug 21, 2026, the average hourly pay for director biotech clinical research in the United States is $54.33, according to ZipRecruiter salary data. Most workers in this role earn between $32.45 and $71.63 per hour, depending on experience, location, and employer.

What does a director of biotech clinical research do?

A Director of Biotech Clinical Research oversees the planning, execution, and management of clinical trials for new biotech products and therapies. They ensure studies comply with regulatory requirements and are conducted ethically and efficiently. This role involves managing cross-functional teams, developing clinical strategies, analyzing data, and collaborating with internal and external stakeholders. Their leadership is crucial in advancing innovative treatments from the laboratory to the market.

What are some common challenges faced by a director of biotech clinical research when overseeing multiple clinical trial phases?

Directors of Biotech Clinical Research often encounter challenges in balancing timelines, budgets, and regulatory compliance across several concurrent trials. Coordinating cross-functional teams—including data management, regulatory affairs, and clinical operations—requires strong leadership and communication skills. Additionally, adapting to unexpected scientific or operational hurdles, such as protocol amendments or patient recruitment delays, is a frequent part of the role. Directors must also ensure adherence to Good Clinical Practice (GCP) standards while fostering innovation and maintaining high-quality results.

What are the key skills and qualifications needed to thrive as a director of biotech clinical research, and why are they important?

To thrive as a Director of Biotech Clinical Research, you need a strong background in clinical research, regulatory affairs, and a relevant advanced degree (PhD, MD, or PharmD are common). Familiarity with clinical trial management systems (CTMS), FDA regulations, GCP guidelines, and often certifications like ACRP or SOCRA are highly valued. Exceptional leadership, strategic planning, and cross-functional communication skills set top performers apart in this role. These skills are critical for ensuring compliance, advancing research goals, and leading successful clinical programs in a complex regulatory environment.

What is the difference between Director Biotech Clinical Research vs Clinical Project Manager?

AspectDirector Biotech Clinical ResearchClinical Project Manager
CredentialsAdvanced degrees (PhD, MD, or MS), industry experienceBachelor's or Master's degree, relevant certifications
Work EnvironmentStrategic leadership, overseeing multiple projectsManaging individual clinical trials, coordinating teams
Employer & Industry UsageBiotech companies, pharmaceutical firmsContract research organizations, biotech, pharma
Search & Comparison IntentHigh-level leadership roles, strategic oversightOperational roles, trial management

The main difference is that the Director Biotech Clinical Research focuses on strategic leadership and overseeing multiple clinical research projects, often requiring advanced degrees and extensive experience. In contrast, a Clinical Project Manager handles the day-to-day management of specific clinical trials, coordinating teams and ensuring trial milestones are met. Both roles are essential in the biotech industry but differ in scope and responsibilities.

More about Director Biotech Clinical Research jobs

What cities are hiring for Director Biotech Clinical Research jobs?

Cities with the most Director 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 Director Biotech Clinical Research jobs?

States with the most job openings for Director Biotech Clinical Research jobs include:

Infographic showing various Director Biotech Clinical Research job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 91% In-person, and 9% Remote job distribution, with an average salary of $113,010 per year, or $54.3 per hour.

Senior Clinical Research Coordinator (CRC)

Smarter HR Solutions LLC

NY • On-site

$90 - $100/hr

Other

Medical, Dental, Vision

Posted 3 days ago

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Job description

Senior Clinical Research Coordinator (CRC)

Full time | Smarter HR Solutions LLC | United States

Posted On 07/27/2026

Job Information

Pharma/Biotech/Clinical Research

Work Experience 4-5 years

$90,000-$100,000 per year

City Orange

State/Province California

92868

Job Description

***Please note: This position is onsite and not remote. Candidates must be based in the Orange, CA area, as relocation assistance is not provided. Only individuals authorized to work in the U.S. will be considered.***

Job Title: Senior Clinical Research Coordinator (Liver Trials)

Job Type: Full-Time | On-Site

Job Location: Orange, CA

Job Salary: $90,000-$100,000 per year (based on experience)

Industry: Clinical Research | Hepatology | Phase I-IV Trials

About Us

Join a fast-paced, compliance-driven research clinic specializing in liver disease trials—from NASH and cirrhosis to hepatocellular carcinoma. The clinic partners with leading sponsors and CROs to deliver high-quality, audit-ready data and compassionate patient care.

Position Overview

This is an on-site position in Orange, CA, and applicants must reside within a commutable distance of 50 miles or less or be able to independently relocate. THIS IS NOT A REMOTE POSITION.

We’re seeking a Senior Clinical Research Coordinator (CRC) with hands‑on experience in liver-focused clinical trials. You’ll lead study execution, regulatory coordination, and patient engagement across multiple protocols.

MUST HAVE - Experience in CRC in Liver/GI/Obesity studies

MUST HAVE - Regulatory experience

MUST HAVE - Fluency in Spanish

Key Responsibilities
  • Coordinate Phase I-IV liver trials, including screening, enrollment, and follow-up
  • Manage regulatory submissions (IRB, CPHS), source documentation, and AE reporting
  • Oversee biospecimen handling and lab coordination
  • Maintain CTMS and EDC systems (REDCap, Medidata, etc.)
  • Mentor junior CRCs and support cross-functional study teams
Requirements Qualifications
  • 3-5+ years of CRC experience in liver/hepatology trials
  • Strong knowledge of FDA, ICH-GCP, and HIPAA regulations
  • Proficiency in CTMS, EDC platforms, and protocol adherence
  • Excellent communication and documentation skills
  • Familiarity with California specific regulations
Certifications
  • CPHS Compliance Training (Required)
  • CCRC (Certified Clinical Research Coordinator) (Preferred)
  • Competitive salary + performance bonuses
  • Health, dental, and vision coverage
  • Paid training and certification support
  • Career growth in a high-impact research setting
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