- Location: New Jersey, United States
- Type: Contract
- Job ID: 10571
- Work Setting: On-Site
- Posted: September 1, 2026
- Closing Date: August 24, 2027
- Tax Status: W2
Non-clinical Scientist Consultant
12 month contract
Remote, EST hours
Join our team as a Scientist Consultant (QC/AS) II and play a pivotal role in advancing innovative pharmaceutical discovery and development. This dynamic position offers the opportunity to lead and support critical nonclinical studies, ensuring the highest standards of scientific excellence and regulatory compliance. If you are passionate about cutting-edge research, meticulous in study management, and eager to contribute to impactful projects, this is the perfect role for you.
What You’ll Do:
Required Skills:
Nice to Have Skills:
Preferred Education and Experience:
12 month contract
Remote, EST hours
Join our team as a Scientist Consultant (QC/AS) II and play a pivotal role in advancing innovative pharmaceutical discovery and development. This dynamic position offers the opportunity to lead and support critical nonclinical studies, ensuring the highest standards of scientific excellence and regulatory compliance. If you are passionate about cutting-edge research, meticulous in study management, and eager to contribute to impactful projects, this is the perfect role for you.
What You’ll Do:
- Assist in managing contract laboratories for nonclinical studies, including study scheduling, sample shipments, archiving, and reporting.
- Coordinate vendor contracts, including MSAs, Quality Agreements, CDAs, and financial agreements.
- Procure and track reference materials at analytical labs and review incoming results for accuracy.
- Provide expert scientific input on study design, data analysis, and interpretation of results, communicating key findings effectively.
- Prepare and maintain QC documentation like protocols, reports, and test methods.
- Conduct audits of external CROs and analytical laboratories to ensure compliance and quality standards.
- Manage study timelines to meet project objectives and QC regulatory documents such as IND, CTA, NDA submission materials.
Required Skills:
- 3-5 years of industrial DMPK experience in pharmaceutical, biotech, or nonclinical CRO environments supporting drug discovery and development.
- Proven expertise in in vitro and/or in vivo study support, with outsourcing experience considered a plus.
- Technical knowledge in preclinical PK, MetID, and/or drug-drug interactions is highly desirable.
- Strong organizational skills and excellent communication capabilities.
Nice to Have Skills:
- Experience with regulatory submission documents and audits.
- Additional expertise in pharmacokinetics, pharmacology, toxicology, or related sciences.
Preferred Education and Experience:
- Bachelor's or Master's degree in Chemistry, Biology, Pharmaceutical Sciences, Pharmacokinetics, Pharmacology, Toxicology, or related fields.
- BS/MS with 3-5 years of industry experience or PhD with at least 2 years of relevant experience.