Bioanalytical Scientist – Lignan Binding Method Dev

1104 Syneos Health Clinical Lab, Inc.; Princeton (NJ); On-site; USD 90,000 - 140,000; Full time

Benefits offered by this job

Company car

Health benefits

401k matching

Stock Purchase Plan

Bonuses

PTO & sick time

Job summary

Syneos Health in New Jersey seeks a Ligan Binding Research Scientist in Clinical Research to coordinate bioanalytical method development, validation, and data interpretation. The role focuses on delivering client-ready methods within project timelines and ensuring regulatory alignment.

You will contribute to method development, literature review, SOP writing, and training within a collaborative Clinical Solutions team. Strong communication and technical skills are essential for success.

Qualifications

• Bachelor's degree in science or equivalent required.
• Experience with regulatory context is an asset.
• Proficient in Word, Excel and data analysis.

Responsibilities

• Coordinate and execute development and validation of bioanalytical methods per client requests and timelines.
• Develop, validate and optimize bioanalytical methods using analytical techniques.
• Process, analyze and interpret bioanalytical data.
• Identify and solve issues related to bioanalytical methods application.
• Assist in improving laboratory processes (method development, validation, sample analysis).
• Write and review method SOPs and related documentation.
• Review literature to guide method development.
• Train staff on research, development and validation activities as needed.

Skills

Bioanalytical method development

Data analysis

Regulatory knowledge

Lab skills

Education

Bachelor's Degree in Science

Tools

Microsoft Word

Excel

Analytical software

Job description

Syneos Health in New Jersey seeks a Ligan Binding Research Scientist in Clinical Research to coordinate bioanalytical method development, validation, and data interpretation. The role focuses on delivering client-ready methods within project timelines and ensuring regulatory alignment.

You will contribute to method development, literature review, SOP writing, and training within a collaborative Clinical Solutions team. Strong communication and technical skills are essential for success.