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Clinical Development Consultant Jobs (NOW HIRING)

Gilead

Director, Clinical Development

Foster City, CA · On-site

$93K - $127K/yr

MD or equivalent with 4+ years' clinical, scientific and/or drug development experience in the biopharma industry, healthcare, consulting, academia or a related environment; OR * PharmD or PhD in ...

Gilead

Director, Clinical Development

Foster City, CA · On-site

$93K - $127K/yr

MD or equivalent with 4+ years' clinical, scientific and/or drug development experience in the biopharma industry, healthcare, consulting, academia or a related environment; OR * PharmD or PhD in ...

PTC Therapeutics

Director, Clinical Development

Warren, NJ · On-site

$83K - $113K/yr

... consultants, etc. As such he/she may author or review clinical/medical-related materials intended ... The Director, Clinical Development ensures adherence to relevant regulatory requirements and ...

Otsuka

Director, Global Clinical Development

$81K - $111K/yr

D. may be considered if complemented by a team or consulting clinician. - Experience in the ... Empowered Development - Play an active role in professional development as a business imperative.

Otsuka

Director, Global Clinical Development

$81K - $111K/yr

D. may be considered if complemented by a team or consulting clinician. * Experience in the ... An advanced understanding of drug development principles and clinical trial implementation ...

Otsuka Pharmaceutical Co., Ltd

$59K - $80K/yr

D. may be considered if complemented by a team or consulting clinician. * Experience in the ... An advanced understanding of drug development principles and clinical trial implementation ...

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Clinical Development Consultant information

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$27K

$96.2K

$169.5K

How much do clinical development consultant jobs pay per year?

As of Sep 15, 2026, the average yearly pay for clinical development consultant in the United States is $96,206.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,000.00 and $114,000.00 per year, depending on experience, location, and employer.

What is a clinical development consultant?

Clinical Development Consultants are professionals who provide expertise and guidance in the planning, execution, and management of clinical trials for pharmaceutical, biotechnology, and medical device companies. They help organizations design study protocols, ensure regulatory compliance, and optimize clinical trial operations to bring new therapies to market efficiently and safely. Their role often involves collaborating with cross-functional teams, overseeing data management, and advising on best practices for clinical development strategies.

What are the key skills and qualifications needed to thrive as a clinical development consultant?

To thrive as a Clinical Development Consultant, you need a solid background in clinical research, regulatory affairs, and drug development, often supported by an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and knowledge of ICH-GCP guidelines and FDA regulations are typically required. Strong project management, problem-solving, and interpersonal communication skills set outstanding consultants apart. These competencies are critical for ensuring clinical trials are efficiently designed, compliant, and successfully executed to advance new therapies to market.

What are some common challenges faced by clinical development consultants and how can they be addressed?

Clinical Development Consultants often navigate complex regulatory requirements, tight project timelines, and cross-functional team dynamics. Balancing the scientific integrity of clinical trials with operational efficiency can be challenging, especially when coordinating among stakeholders such as sponsors, regulatory bodies, and clinical sites. Building strong communication skills, staying updated on regulatory changes, and fostering collaborative relationships can help address these challenges and ensure successful project outcomes.

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

AspectClinical Development ConsultantClinical Research Associate
Required CredentialsTypically advanced degrees (e.g., MSc, PhD), industry experience, certifications like CCRP or RACBachelor’s degree, often with certifications like CRA or CCRA
Work EnvironmentConsulting firms, pharmaceutical companies, biotech firms; involved in strategic planning and project oversightClinical trial sites, hospitals, research centers; focused on site monitoring and data collection
Employer & Industry UsageUsed by consulting agencies and pharma companies for project-based rolesCommonly employed by CROs, pharmaceutical companies, and research sites

While both roles are integral to clinical research, a Clinical Development Consultant focuses on strategic planning, regulatory compliance, and project management at a higher level, often working across multiple projects. In contrast, a Clinical Research Associate primarily conducts site monitoring, data verification, and ensures trial adherence at specific sites. Understanding these differences helps in choosing the right career path or job search focus.

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What cities are hiring for Clinical Development Consultant jobs?

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What are popular job titles related to Clinical Development Consultant jobs?

For Clinical Development Consultant jobs, the most frequently searched job titles are:

Infographic showing various Clinical Development Consultant job openings in the United States as of June 2026, with employment types broken down into 1% Internship, 3% As Needed, 89% Full Time, 1% Part Time, 1% Temporary, and 5% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $96,206 per year, or $46.3 per hour.

Clinical Development Consultant

Rochester, NY • On-site

Motion Recruitment Partners, LLC
Recruiting and Staffing Services • 1 - 5K employees
Learn more about Motion Recruitment Partners, LLCexternal

Other

Posted 3 days ago

New

Job description

Kelly Science and Clinical FSP is currently seeking a Clinical Development Consultant for an engagement with one of our Global Pharmaceutical partners. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc.
Clinical Development Consultant- position in R&D
Responsibilities
  • Serve as a strategic thought partner to the Head of Development and a clinical thought leader for the MetALD program, while supporting the ongoing severe alcohol-associated hepatitis program and potentially other liver disease initiatives.
  • MD required; board-certified hepatologist is preferred. Candidates with internal medicine training or other relevant specialties, significant pharmaceutical industry experience in hepatology clinical development, and expertise in MASH/NASH and MetALD will also be considered.
  • Be a hands-on clinical developer who can author clinical protocols and other key study documents, working collaboratively with the development to design and operationalize the MetALD Phase 2 program.
  • ~10 years of relevant pharma industry clinical development experience.

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