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Clinical Development Scientist Jobs (NOW HIRING)

Elanco

Research Scientist

Indianapolis, IN · Hybrid

Clinical Development Scientist - Farm Animal As a Clinical Development Scientist, you will lead the development and execution of global farm animal clinical programs supporting Elanco's innovation ...

Catalent, Inc.

Development Scientist I

Greenville, NC · On-site

The Development Scientist I will serve as the primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities. The Development ...

Merck & Co.

Principal Scientist (Director) in Translational Medicine-Oncology Translational Medicine at our ... Development and execution of clinical pharmacology strategies to support later stages of ...

Catalent, Inc.

Development Scientist II

Greenville, NC · On-site

The Development Scientist II is responsible for supporting these activities in the areas of supervision, process development, clinical trial batch manufacturing, packing and documentation. Position ...

Merck & Co.

Principal Scientist (Director) in Translational Medicine-Oncology Translational Medicine at our ... Development and execution of clinical pharmacology strategies to support later stages of ...

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Clinical Development Scientist information

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How much do clinical development scientist jobs pay per hour?

As of Jul 17, 2026, the average hourly pay for clinical development scientist in the United States is $54.75, according to ZipRecruiter salary data. Most workers in this role earn between $40.14 and $68.27 per hour, depending on experience, location, and employer.

How does a Clinical Development Scientist typically collaborate with cross-functional teams during a clinical trial?

Clinical Development Scientists play a central role in coordinating with various teams such as clinical operations, regulatory affairs, data management, and biostatistics throughout a clinical trial. They ensure that clinical protocols are scientifically sound and align with regulatory requirements, while also facilitating clear communication between departments to address study challenges and maintain timelines. By serving as the scientific point of contact, they help integrate input from multiple stakeholders, support troubleshooting during trial execution, and contribute to the preparation of study documents and data analysis.

What does a Clinical Development Scientist do?

A Clinical Development Scientist is responsible for designing, planning, and overseeing clinical trials that test new drugs, therapies, or medical devices. They collaborate with cross-functional teams to ensure that clinical studies are scientifically sound, compliant with regulations, and aligned with strategic objectives. Their work involves protocol development, data analysis, and interpretation of results to support regulatory submissions and product approvals. Ultimately, they play a key role in bringing safe and effective treatments to patients.

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

AspectClinical Development ScientistClinical Research Associate
Required credentialsBachelor's or Master's in Life Sciences, relevant certificationsBachelor's in Life Sciences or related field, often with certification in clinical trials
Work environmentDesigning and planning clinical trials, collaborating with teamsMonitoring clinical trials at sites, ensuring protocol compliance
Employer and industry usagePharmaceutical companies, biotech firms, CROsPharmaceutical companies, CROs, research institutions
Common search and comparison intentUnderstanding roles in clinical developmentMonitoring and managing clinical trial sites

The Clinical Development Scientist focuses on designing, planning, and analyzing clinical trials, working closely with research teams. In contrast, the Clinical Research Associate primarily monitors trial sites to ensure compliance and data integrity. Both roles are essential in clinical research but differ in responsibilities and daily tasks.

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

To thrive as a Clinical Development Scientist, you need a solid background in life sciences, clinical research methodologies, and drug development, often supported by an advanced degree such as a PhD or PharmD. Familiarity with regulatory requirements, clinical trial management systems (CTMS), and data analysis tools is essential. Strong analytical thinking, attention to detail, and effective communication skills help you collaborate cross-functionally and drive successful clinical studies. These skills ensure rigorous study design, regulatory compliance, and effective advancement of new therapies through clinical pipelines.
More about Clinical Development Scientist jobs
What cities are hiring for Clinical Development Scientist jobs? Cities with the most Clinical Development Scientist job openings:
What states have the most Clinical Development Scientist jobs? States with the most job openings for Clinical Development Scientist jobs include:
What job categories do people searching Clinical Development Scientist jobs look for? The top searched job categories for Clinical Development Scientist jobs are:
Clinical Development Scientist jobs near you
Infographic showing various Clinical Development Scientist job openings in the United States as of July 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $113,877 per year, or $54.7 per hour.

Clinical Scientist, Clinical Development

Spyre Therapeutics

Remote

$215K - $230K/yr

Full-time

Medical, Retirement, PTO

Posted 3 days ago

New

Job description

Spyre Therapeutics is a clinical-stage biotechnology company committed to developing next-generation therapies that elevate the standard in immunology by delivering more complete disease control, greater durability, and a simpler treatment experience for patients. Spyre's pipeline includes investigational extended half-life antibodies targeting α4β7, TL1A, and IL-23.
Role Summary:
As a Director, Clinical Scientist at Spyre Therapeutics, you will play a key role in designing, executing, and interpreting clinical trials that support development of our novel antibody-based therapies in rheumatic and/or other I&I diseases. You will collaborate across functions (clinical operations, regulatory, translational science, biomarker teams) to ensure robust study designs, high-quality data generation and efficient progression of programs. You will bring scientific and operational expertise and act as a bridge between internal teams, external investigators and CRO partners.
Key Responsibilities:
  • Lead/Contribute to study design and amendments in collaboration with internal and external stakeholders.
  • Collaborate with Clinical Development, regulatory and other internal partners/stakeholders with authoring and submission of protocols, protocol amendments, regulatory filings, and other regulatory documentation.
  • Collaborate with clinical operations, data management and CRO to develop and implement the overall data quality plan and lead internal medical data review and safety trend analysis on one or more studies/programs.
  • Work closely with translational science/biomarker teams to integrate mechanistic biomarkers, PK/PD modelling, patient stratification, and exploratory endpoints.
  • Provide scientific oversight and decision-making support during trial execution: site selection, study start-up, monitoring of key trial metrics, risk-based quality oversight and study close-out.
  • Interpret clinical data (safety, efficacy, biomarker, PK/PD) and present findings internally (e.g., to senior management or clinical development committee) and externally (investigators, scientific meetings, publications).
  • Write and/or review abstracts, posters, content for scientific meetings, conferences, other events and presentations, and other publicly distributed materials and coordinate further reviews with internal partners and stakeholders.
  • Write clinical science sections of meeting packages and assist in the development and review of other clinical documentation required for regulatory submissions and other regulatory processes
  • Collaborate with regulatory affairs to ensure study designs meet regulatory standards (e.g., FDA/ICH, GCP) and support regulatory submissions and interactions.
  • Develop and maintain clinical trial documentation (protocols, clinical study reports, investigator brochures, informed-consent forms, etc.).
  • Monitor the competitive and scientific landscape in therapeutics space and contribute to strategic positioning of Spyre's pipeline programs.
  • Additional duties as assigned.

Ideal Candidate:
  • PhD, MD, PharmD or equivalent in life sciences, clinical pharmacology, immunology or related discipline is preferred; alternatively, MSc plus significant industry experience.
  • 5+ years (or more for senior levels) of clinical development experience in the biotech/pharma industry, ideally with at least 2 years in rheumatology , or other immune-mediated disease area.
  • Demonstrated experience designing and executing clinical trials in rheumatology, or other I&I therapeutic area.
  • Strong understanding of clinical biomarkers, PK/PD modelling, patient stratification and immunologic endpoints.
  • Familiarity with regulatory requirements (FDA/ICH guidelines, GCP) and Good Clinical Practice.
  • Proven ability to work cross-functionally in a matrix organization (clinical operations, translational science, regulatory, QA).
  • Excellent written and verbal communication skills, presentation and interpersonal skills; ability to influence diverse stakeholders.
  • Comfortable working in a fast-paced, dynamic environment with ambiguity, and willing to wear multiple hats.

What We Offer:
  • Opportunity to work in a fast-paced, dynamic environment where you help shape the culture of our young company, contribute broadly to advance meaningful medicines, and learn quickly.
  • Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits.
  • Unlimited PTO
  • Two, one-week company-wide shutdowns each
  • Commitment to provide professional development opportunities.
  • Remote working environment with frequent in-person meetings to address complex problems and build relationships.

The expected salary range offer for this role is $215,000 to $230,000. Actual pay offered may vary depending on job related knowledge, experience, education, and geographic location.
As an equal opportunity employer, Spyre is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment designed to create a stronger and better Spyre that is focused on developing life-changing products for patients.
Spyre Therapeutics, along with other biotech companies, has become aware of a surge in email scams targeting prospective job candidates within our industry. Please be aware that official recruiters at Spyre Therapeutics only use email addresses with the domain "@spyre.com." We want to also emphasize that we never request candidates to make any purchases or divulge sensitive personal information via email.
Please also be aware that all job postings will be listed on our website at spyre.com/careers/.

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