Scientist Consultant

Real; Trenton (NJ); Hybrid; USD 90,000 - 130,000; Full time

Job summary

Real is seeking a qualified DMPK professional to support drug discovery and development in a collaborative, science-driven environment. Remote with a hybrid option in New Jersey, the role focuses on nonclinical studies and ensuring timely data delivery.

The ideal candidate has 3–5 years of industry DMPK experience, expertise in PK/MetID/DDI, and strong organizational skills. BS/MS or PhD with relevant experience is preferred.

Qualifications

• 3-5 years of industrial DMPK experience in pharma/biotech/CRO.
• Experience with in vitro/in vivo study support; outsourcing a plus.
• Expertise in preclinical PK, MetID, and/or DDI highly desirable.
• Strong organizational and communication skills.
• BS/MS with 3-5 years industrial experience or PhD with 2+ years.

Responsibilities

• Assist with management of contract labs for nonclinical studies.
• Manage study scheduling, shipment of study materials, archiving records, and reporting activities.
• Coordinate implementation of vendor contracts (MSAs, Quality Agreements, CDAs, Financial Agreements).
• Procure and track transfer of reference materials at contract analytical labs.
• Review incoming study results for accuracy in execution, data collection, and data analysis.
• Provide scientific input on study design, review, and interpretation of results.
• Prepare and maintain QC documentation (protocols, reports, test methods).
• Audit external nonclinical CROs including analytical laboratories.
• Manage study timelines to meet broader project needs.
• Perform QC of regulatory documents (IND, CTA, briefing book, NDA).

Skills

Study monitoring

Contract management

Study scheduling

Regulatory document QC

Communication skills

Education

BS/MS in Chemistry/Biology or related

PhD with 2+ years experience

Tools

MSAs

Quality Agreements

CDAs

Financial Agreements

Job description

Location:

Remote (Hybrid option available in New Jersey)

About the Opportunity:

Our client is a leading global pharmaceutical organisation focused on advancing innovative therapies for patients with significant unmet medical needs. This role offers the opportunity to support drug discovery and development programs within a collaborative, science-driven environment.

Location:

Remote (Hybrid option available in New Jersey)

Contract Length:

12 Months

About the Opportunity:

Our client is a leading global pharmaceutical organisation focused on advancing innovative therapies for patients with significant unmet medical needs. This role offers the opportunity to support drug discovery and development programs within a collaborative, science-driven environment.

Key Responsibilities Include:

• Study monitoring: Assists with the management of contract laboratories with regards to the execution of nonclinical studies for Discovery and Development compounds.
• Manage study scheduling and timelines, shipment of study materials, archiving internal study records, and reporting and associated activities
• Coordinate the implementation of vendor contracts (MSAs, Quality Agreements, CDAs, Financial Agreements)
• Procure and track the transfer of reference materials at contract analytical laboratories
• Review incoming study results for accuracy in study execution, data collection, and data analysis.
• Provide scientific input on study design, review, and interpret study results, and communicate key findings.
• Prepare and maintain QC documentation, including protocols, reports and test methods.
• Audit external Nonclinical CROs including analytical laboratories
• Manage study timelines to meet the broader project needs
• Perform QC of regulatory documents (IND, CTA, briefing book, NDA, etc)

Qualifications:

• 3-5 years of industrial DMPK experience in the pharmaceutical industry, either in Pharma, Biotechnology, or a Nonclinical CRO supporting drug discovery and development programs.
• Demonstrated expertise in in vitro and/or in vivo study support necessary, and experience outsourcing studies desired.
• Technical expertise in preclinical PK, MetID, and/or drug-drug interactions highly desirable.
• Excellent organisational and communication skills required.
• Education: Degree in Chemistry, Biology, or the Pharmaceutical Sciences (Pharmacokinetics, Pharmacology, Toxicology, or related science). BS, MS with 3-5 years industrial experience or PhD with 2+ years' experience.

EOE Statement

Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.