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60 Incyte Clinical Research Associate Jobs Hiring Near You

Incyte Corporation

Animal Care Technician II/III

Wilmington, DE · On-site

$15.25 - $20.50/hr

Incyte is committed to the rigorous pursuit of research and development excellence to improve the ... Bachelor degree in Life Sciences, Associate degree or certificate program in the life sciences with ...

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

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What are some common challenges Clinical Research Associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

What are Clinical Research Associates?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

Is it hard to get a CRA job?

Securing a Clinical Research Associate (CRA) position can be competitive, often requiring relevant education such as a degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and certifications like CCRP can improve job prospects, but entry may be challenging for those without related experience or training.

What is the difference between Clinical Research Associate vs Clinical Trial Coordinator?

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

What other companies are hiring for Clinical Research Associate jobs?
What are the most popular jobs at Incyte?
What are the most popular categories at Incyte?
Infographic showing various Clinical Research Associate job openings at Incyte in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 95% Physical, and 5% Remote job distribution.
Research Expert / Research Investigator - Biotransformation (Metabolite Identification), DMPK

Research Expert / Research Investigator - Biotransformation (Metabolite Identification), DMPK

Incyte Corporation

Wilmington, DE • On-site

$45.10K - $45.60K/yr

Full-time

Posted 27 days ago

Job description

Overview
A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity
Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
The Biotransformation group within Drug Metabolism and Bioanalysis (DMB) supports discovery and development programs through characterization of drug metabolism and disposition.
We are seeking an experienced scientist who has the flexibility to provide hands-on (lab-based) support of biotransformation (metabolite identification) activities across a portfolio of small molecule programs. The incumbent will contribute to metabolite identification and data interpretation for compounds during optimization and development, while scientifically and strategically interfacing with other DMPK colleagues as well as Medicinal Chemistry partners.
Essential Functions of the Job (Key responsibilities)
  • Conduct in vitro and in vivo biotransformation studies, including hepatocyte, microsomal, and radiolabeled (e.g., 14C) ADME investigations
  • Perform metabolite identification using LC-MS/MS and high-resolution mass spectrometry platforms (e.g., Orbitrap, QTOF)
  • Analyze and interpret mass spectrometry data to characterize metabolic pathways and identify potential liabilities
  • Serve as the biotransformation representative on assigned discovery program(s), with level of independence commensurate with experience
  • Generate and communicate metabolite identification results to support medicinal chemistry and program decision-making
  • Support development programs through analysis and reporting of preclinical and clinical ADME studies, including mass balance and human ADME studies
  • Prepare and review technical reports and contribute to regulatory documents (IND/NDA) as appropriate
  • Collaborate with cross-functional teams and coordinate external CRO activities as needed

Qualifications (Minimal acceptable level of education, work experience, and competency)
  • Ph.D. in Pharmaceutical Sciences, Chemistry, Biochemistry, or a related discipline with 0-5+ years of relevant industry or postdoctoral experience
    or
  • M.S. with 4-8+ years of relevant industry experience
    or
  • B.S. with 6-10+ years of relevant industry experience
  • Experience in biotransformation and metabolite identification in a pharmaceutical or CRO environment
  • Hands-on experience with in vitro metabolism systems (e.g., hepatocytes, microsomes)
  • Experience interpreting LC-MS/MS or high-resolution MS data for metabolite identification
  • Experience working with or supporting radiolabeled (e.g., 14C) ADME studies, including sample handling, data generation, or interpretation
  • Strong understanding of drug metabolism pathways (e.g., CYP, UGT)
  • Ability to analyze complex data and clearly communicate findings to matrix team members

Preferred Qualifications
    • Experience contributing to regulatory submissions (IND/NDA)
    • Familiarity with metabolite identification software (e.g., UNIFI, Compound Discoverer, MassMetaSite)
    • Experience working in a cross-functional drug discovery environment

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
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