Clinical Development Scientist (Biology) | Remote

Crossing Hurdles; United States; Remote; USD 151,536 - 185,976; Part time

Job summary

A biotechnology company is looking for a Translational Biology Expert in the United States. In this project-based role, you will design and evaluate preclinical studies, develop biomarker strategies, and contribute to early clinical program design. Candidates must have an advanced academic qualification in pharmacology or related fields and relevant industry experience. Strong communication skills and expertise in interpreting complex biological datasets are essential for success in this role.

Qualifications

• Advanced degree in pharmacology, pharmaceutical sciences, or quantitative biology required.
• Industry experience in pharmaceutical or biotechnology environments is essential.
• Experience supporting programs from late preclinical to early clinical development is a must.

Responsibilities

• Design and evaluate preclinical studies linking molecular mechanisms to disease outcomes.
• Develop biomarker strategies that connect target engagement with clinical response.
• Contribute to early clinical program design including dose selection.

Skills

Interpreting complex biological datasets

Strong communication skills

Quantitative pharmacology approaches

Translational biomarkers knowledge

Education

Advanced academic qualification in pharmacology or related fields

Job description

Overview

Position: Translational Biology Expert

Type: Hourly contract

Compensation: $110-$135 per hour

Commitment: Project Based

Responsibilities

• Design and evaluate preclinical studies linking molecular mechanisms to disease-relevant outcomes
• Select appropriate experimental systems including in vitro, ex vivo, and animal models to support translational research
• Develop biomarker strategies that connect target engagement with clinical response
• Interpret preclinical datasets to guide decision-making and refine mechanistic hypotheses
• Assess safety signals, immunogenicity risks, and biological drivers of unexpected experimental outcomes
• Contribute to early clinical program design including dose selection, patient stratification, and endpoint selection
• Apply quantitative pharmacology approaches such as exposure-response analysis and PK/PD modeling
• Support statistical planning, interim analysis design, and evidence-based development decisions

Requirements

• Advanced academic qualification in pharmacology, pharmaceutical sciences, quantitative biology, biostatistics, or related biomedical fields
• Industry experience in pharmaceutical, biotechnology, or contract research environments
• Direct experience supporting programs from late preclinical stages into early clinical development
• Strong expertise in interpreting complex biological and pharmacological datasets
• Familiarity with translational biomarkers, pharmacokinetics, and clinical study design principles
• Ability to develop clear scientific recommendations based on incomplete or evolving data
• Strong communication skills for presenting technical insights to cross-functional teams

Application Process

• Upload resume
• Interview (15 min)
• Submit form