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Clinical Development Biotech Jobs (NOW HIRING)

Amgen, Inc.

Clinical Development Director - Oncology

$81K - $111K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Clinical Development Director - Oncology What you will do Let's do this. Let's change the world. In ...

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How much do clinical development biotech jobs pay per hour?

As of Jun 15, 2026, the average hourly pay for clinical development biotech 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 clinical development in biotech?

Clinical development in biotech refers to the process of testing new drugs or therapies in human participants to determine their safety and effectiveness. This phase follows preclinical research and involves multiple stages of clinical trials, from Phase I (safety) to Phase III (efficacy and monitoring of side effects). Clinical development professionals coordinate the design, implementation, and analysis of these studies, ensuring compliance with regulatory standards. Their work is crucial in bringing innovative treatments from the laboratory to patients. Success in this field requires knowledge of medical science, regulatory guidelines, and project management.

What are the typical challenges faced by professionals working in clinical development within the biotech industry?

Professionals in clinical development for biotech companies often encounter challenges related to navigating complex regulatory requirements, managing tight timelines, and ensuring robust data quality across clinical trials. Additionally, frequent cross-functional collaboration is needed, as teams work closely with regulatory affairs, medical affairs, and data management to drive studies forward. Adapting to evolving scientific advancements and shifting project priorities are also common, so flexibility and strong communication skills are essential for success in this fast-paced environment.

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

AspectClinical Development BiotechClinical Research Associate
Required CredentialsBachelor's or higher in life sciences, relevant certificationsBachelor's in life sciences, often with CRA certification
Work EnvironmentPharmaceutical/biotech companies, labs, clinical trial teamsMonitoring sites, clinical trial sites, sponsor offices
Employer & Industry UsageBiotech firms, pharmaceutical companies, CROsPharmaceutical companies, CROs, research organizations
Common Search & ComparisonYesYes

The Clinical Development Biotech role focuses on planning and managing clinical trials within biotech companies, often involving protocol development and regulatory submissions. In contrast, a Clinical Research Associate primarily monitors clinical trial sites to ensure compliance and data integrity. While both roles require similar educational backgrounds and certifications, their daily responsibilities and work environments differ, with the former being more involved in trial design and the latter in trial oversight.

What are the key skills and qualifications needed to thrive as a Clinical Development professional in biotech, and why are they important?

To thrive in Clinical Development within biotech, you need a strong background in life sciences, clinical trials management, and regulatory compliance, often supported by an advanced degree (e.g., PhD, PharmD, or MD). Proficiency with clinical trial management systems (CTMS), data analysis tools, and familiarity with ICH-GCP guidelines and FDA regulations are typically required. Strong project management, communication, and problem-solving skills help navigate complex studies and multidisciplinary teams. These competencies are essential to ensure safe, efficient, and compliant development of new therapies from concept to market.
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Clinical Development Biotech jobs near you
Infographic showing various Clinical Development Biotech job openings in the United States as of June 2026, with employment types broken down into 6% Full Time, 63% Part Time, and 31% 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.

Vice President, Clinical Development

GondolaBio Service Co, Inc.

Palo Alto, CA • On-site

$288K - $380K/yr

Full-time

PTO

Posted 16 days ago

Be an early applicant

Job description

Description:

Company Background

GondolaBio is a collection of biopharmaceutical companies focused on developing next-generation therapeutics for genetic diseases. Originally carved out of BridgeBio, GondolaBio secured $300M in private financing from external investors in 2024 and became an independent company within the BridgeBio ecosystem. GondolaBio aims to leverage cutting-edge biological research to discover, create, test, and deliver transformative medicines to treat patients who suffer from genetic diseases.

One of GondolaBio’s subsidiaries is an early preclinical stage biotechnology company developing a novel best-in-class therapeutic for a rare, severe genetic disease, advancing toward first-in-human clinical studies.


Who You Are

We seek a top clinical development executive to be responsible for building and executing the clinical development plan for our lead program. This role will be primarily accountable for clinical trial execution encompassing study design, oversight and management. This job requires excellent communication and interpersonal skills as well as medical monitoring, clinical operations, KOL and investigator engagement, and drug safety experience. This role will serve as the first dedicated clinical development leader for the program.

Requirements:

Responsibilities

  • Design scientifically rigorous, innovative, and cost-effective clinical development programs, integrating preclinical, translational, and biomarker strategies
  • Direct and oversee the efficient implementation of all clinical projects, including defining initial clinical endpoints, dose-escalation strategies, and patient selection approaches
  • Lead development and contribute to review of Clinical Study Protocols, Clinical Study Reports, Investigator’s Brochures, and all clinical documentation for regulatory filings
  • Become an internal expert on all medical features of the disease area, including natural history, patient diagnostic journey, standards of care, and current development programs.
  • Build, mentor, and scale the clinical development and clinical operations teams, including defining structure, capabilities, and external partnerships appropriate for each stage of the program
  • Provide leadership and clinical development expertise to the overall organization, including the clinical development, clinical operations, biometrics, toxicology, and translational science teams
  • Collaborate with Regulatory Affairs to develop strategies and tactical work plans during clinical development and in preparation for the anticipated US and global filings
  • Lead the preparation and management of clinical information to support timely regulatory submissions, including INDs, briefing documents, and early clinical protocols
  • Set a high standard and example of urgency, work quality, and effectiveness
  • Contribute to due diligence and gap analysis on potential new GondolaBio assets
  • Partner closely with discovery and preclinical teams to ensure clinical readiness for first-in-human studies.
  • Perform all other duties as assigned


Education, Experience & Skills Requirements

  • Doctorate Degree in Medicine (MD) is required for the position.
  • A proven leader with minimum of 10 years pharmaceutical/biotechnology industry experience in all phases of drug development
  • Deep knowledge of the drug development process with a focus on clinical study design and management; ability to collaborate with, support, and oversee CROs
  • Able to drive strategic thinking and plans for successful clinical trial outcomes
  • Experience interfacing with the global regulatory authorities (incl. FDA, EMA) and respective standards, including hands-on experience in global drug development
  • Recent experience of IND and NDA/BLA submissions strongly preferred
  • Dynamic individual with excellent written, communication, and interpersonal skills
  • Ability to deliver effective presentations both internally and externally, and strong networking abilities and creativity
  • Ability to set priorities, work independently and deliver high-quality results with urgency
  • Vital planning, organizational, and leadership skills
  • Results-oriented. Strong initiative, accountability, and willingness to take ownership and drive projects to completion
  • Experience in driving collaborations and working with external partners, including building networks with key opinion leaders (KOL) and investigators, business partners
  • Proven ability to build, mentor, and scale clinical development teams over time
  • Able to proactively identify and solve problems under pressure
  • Motivated to work in a fast-paced, highly accountable, small company environment. A "can do" and collegial professional who leads through influence and interpersonal skills. Demonstrated matrix leadership skills and ability to collaborate successfully with multiple functions and external vendors in a cross-functional team environment
  • Solid critical, strategic, and analytical thinking skills
  • Travel required

What We Offer:

  • Patient Days, where we are fortunate enough to learn more about the lives we are looking to impact and a real exchange of ideas as to how we can improve our efforts
  • A culture inspired by our values: put patients first; think independently; be radically transparent; every minute counts; and let the science speak
  • Collaborative business environment
  • Excellent compensation package (Base, Performance Bonus, Equity)
  • Excellent benefits package
  • Flexible PTO
  • A fast-paced, data-driven, work environment with world-class R&D minds and capabilities
  • Work with the most productive groups of R&D operators in the industry
  • A platform for meaningful scientific contributions to shine

"GondolaBio ServiceCo is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. Employees of BridgeBio and all affiliated companies should work through their managers to inquire about and learn more about this role."


The base pay range for this position is $288,000 to $380,000 per year. The actual compensation offered will be determined based on a number of job-related factors, including experience, skills, qualifications, and location. A bonus plan and equity will also be offered.