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Preclinical Development Jobs in Raleigh, NC (NOW HIRING)

IQVIA

Clinical Trial Lead

Durham, NC · On-site +1

Train and support staff on clinical trial processes, systems, and competency frameworks to foster continuous development. Consult with pharmacogenetics and safety experts on preclinical data, adverse ...

AskBio

Associate Scientist, Immunology

Durham, NC · On-site

Speak with your direct manager to discuss your interest and alignment with your development goals ... on preclinical and clinical samples to support our gene therapy programs. This position requires ...

IQVIA, Inc.

Clinical Trial Lead

Durham, NC · On-site

... development. • Consult with pharmacogenetics and safety experts on preclinical data, adverse events (SAEs, SUSARs), and side effect profiles as needed. • Demonstrate therapeutic area expertise (e ...

AskBio

Associate Scientist, Immunology

Durham, NC

Speak with your direct manager to discuss your interest and alignment with your development goals ... on preclinical and clinical samples to support our gene therapy programs. This position requires ...

IQVIA

Clinical Trial Lead

Durham, NC · On-site +1

Train and support staff on clinical trial processes, systems, and competency frameworks to foster continuous development. Consult with pharmacogenetics and safety experts on preclinical data, adverse ...

UNC-Chapel Hill

Open Rank

Chapel Hill, NC

... development. The University offers an array of modern Core facilities for preclinical and clinical research ( UNC Chapel Hill is ranked eleventh in the US based on federal research. We offer a rich ...

Veranex

Sr Clinical Research Associate

Raleigh, NC · On-site

$98K - $140K/yr

... and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting. The Veranex Clinical Operations team is a dynamic group of ...

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Preclinical Development information

See Raleigh, NC salary details

$32.1K

$82.7K

$125.4K

How much do preclinical development jobs pay per year?

As of Aug 20, 2026, the average yearly pay for preclinical development in Raleigh, NC is $82,671.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,900.00 and $87,500.00 per year, depending on experience, location, and employer.

What is preclinical development?

A Preclinical Development job involves overseeing the research and testing of drug candidates before they enter clinical trials. Professionals in this role design and conduct studies to assess a drug’s safety, efficacy, and pharmacokinetics using laboratory and animal models. They collaborate with scientists, regulatory experts, and project managers to generate data required for regulatory approval. Their work helps identify potential risks and optimize drug formulations before human testing begins.

What are the typical responsibilities of someone working in preclinical development?

Professionals in Preclinical Development are responsible for designing, conducting, and analyzing laboratory and animal studies to evaluate the safety and efficacy of new drug candidates before clinical trials. They often collaborate closely with research scientists, regulatory teams, and project managers to ensure studies meet compliance standards and scientific objectives. Daily tasks may include developing protocols, interpreting data, preparing regulatory documentation, and troubleshooting experimental issues. This role offers opportunities to gain broad exposure to the drug discovery process and can lead to advancement into project leadership or regulatory affairs positions.

What are the key skills and qualifications needed to thrive in preclinical development, and why are they important?

To excel in Preclinical Development, you need a solid background in biology, pharmacology, or related life science fields, often supported by an advanced degree and experience with laboratory research. Familiarity with Good Laboratory Practice (GLP) regulations, data analysis software, and animal study management systems is expected. Strong attention to detail, effective problem-solving skills, and the ability to communicate complex findings clearly are valuable soft skills. These competencies are essential to ensure the successful and compliant progression of drug candidates toward clinical trials.

What are the most commonly searched types of Preclinical Development jobs in Raleigh, NC?

The most popular types of Preclinical Development jobs in Raleigh, NC are:

What are popular job titles related to Preclinical Development jobs in Raleigh, NC?

For Preclinical Development jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Preclinical Development jobs in Raleigh, NC look for?

The top searched job categories for Preclinical Development jobs in Raleigh, NC are:

Preclinical Development jobs near you
Infographic showing various Preclinical Development job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $82,671 per year, or $39.7 per hour.

Business Intelligence Analyst

KBI Biopharma, Inc.

Durham, NC • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

KBI Biopharma rating

6.5

Company rating: 6.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI, where innovation meets impact.
Position Summary:
Join a highly technical analytical team in a dynamic work environment as a member of the Analytical, Formulation and Stability (AFS) department and participate in contracted client analytical programs for monoclonal antibodies, recombinant proteins, and peptides as a Business Intelligence Analyst. The Business Intelligence Analyst will provide support to their department and/or the Global CAPS organization by conducting data analysis as it relates to financial performance, metric tracking, capacity modelling, financial forecasting, adherence to budget and portfolio analyses. Role will work closely with departmental leadership in preparation of annual budget and mid-term plan and coordinate with other departments as needed (i.e. Finance, PMO, Business Development).
Position Responsibilities:
  • Assists with contractual and financial execution of projects, including proposals, change orders, revenue recognition, and monthly budget review. Includes review of costs and identifying errors and/or misallocations for spend and working with finance to resolve and support of CapEx forecasting and management.
  • Support business development new business forecasting, capacity planning, program on-boarding, and deliverable delivery. May support drafting or review of proposals and change orders and/or tracking and monitoring of scopes of work.
  • Analyzes complex business problems and issues using data from internal and external sources to provide insight to decision-makers. Identifies and interprets trends and patterns in datasets to locate influences. Constructs forecasts, recommendations and strategic/tactical plans based on business data and market knowledge. Creates specifications for reports and analysis based on business needs and required or available data elements. May provide consultation to users and lead cross-functional teams to address business issues. May directly produce datasets and reports for analysis using system reporting tools.
  • Special cross-group/functional projects
  • Champions, maintains, and publishes key departmental performance metrics
  • Assists development of annual budget and MTP
  • Able to react to change productively and handle other essential tasks as assigned.

Position Requirements:
  • Minimum requirement BS/BA degree and 3-5 years of experience; MBA and/or PMP preferred.
  • Interpersonal soft skills and ability to work well with a diverse group of contributors.
  • Business acumen & long-term planning viewpoint, ability to problem solve and set priorities.
  • Demonstrated experience in project management, coordination of cross-functional teams.
  • High integrity and personal responsibility, action oriented.
  • Excellent written & oral communication and presentation skills.
  • Knowledge of biologics industry is preferred but not required.

About KBI:
KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and Europe. For more information, visit www.kbibiopharma.com.
KBI is a proud EEO/AA employer dedicated to building a diverse and inclusive workforce. We believe that innovation thrives in an environment where all voices are heard and valued. That's why we actively seek individuals from all backgrounds - regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability, or veteran status - and strongly encourage all qualified candidates to apply and bring their unique perspectives to our team.
KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.
I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

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