Senior Clinical Research Scientist

Hartmann Young; Troy (VA); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Job summary

A leading innovator in life sciences in Troy, Virginia, seeks a Senior Research Scientist & Clinical Trials Manager. This role involves leading clinical trials, managing budgets, and collaborating with various teams. The ideal candidate should have an advanced scientific degree, extensive clinical research experience, and strong project management skills. Benefits include medical and vision insurance, as well as a 401(k).

Qualifications

• 5+ years’ experience in clinical research and trial execution.
• Strong background in life sciences, ideally in enzymes or microbiome research.
• Proven experience in managing projects and budgets.

Responsibilities

• Lead and manage clinical trials from initiation through completion.
• Identify and oversee trial sites, including site visits.
• Manage trial budgets and timelines, reporting to stakeholders.

Skills

Clinical research experience

Project and budget management

Communication skills

Technical writing

Willingness to travel

Education

Advanced degree (PhD, MD, PharmD, or equivalent)

Job description

Overview

Hartmann Young is partnering with a leading innovator in the enzyme and life sciences sector to appoint a Senior Research Scientist & Clinical Trials Manager. This role will be based in Troy, Virginia (relocation support available) and offers the opportunity to lead clinical programs and research projects that have global impact.

Responsibilities

• Lead and manage clinical trials from initiation through completion, ensuring compliance with regulatory and ethical standards.
• Identify, evaluate, and oversee trial sites, including site visits as needed.
• Manage trial budgets, timelines, and reporting to executive stakeholders.
• Contribute to research projects with high-quality data collection, analysis, and interpretation.
• Author and review manuscripts, patents, and technical publications.
• Collaborate with regulatory, compliance, and R&D teams on claims substantiation and documentation.
• Provide technical training to internal stakeholders and represent the company at conferences, client meetings, and industry events.

Qualifications & Experience

• Advanced degree (PhD, MD, PharmD, or equivalent) in a relevant scientific discipline.
• 5+ years’ experience in clinical research, trial execution, and manuscript preparation.
• Strong background in life sciences, ideally in enzymes, nutrition, or microbiome research.
• Proven project and budget management experience.
• Excellent written and verbal communication skills, including public speaking and technical writing.
• Knowledge of enzyme functions and applications desirable.
• Requires willingness to travel for trial site visits, conferences, and client meetings.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Research, Science, and Project Management

Industries

• Health and Human Services, Food and Beverage Manufacturing, and Pharmaceutical Manufacturing

Benefits

• Medical insurance
• Vision insurance
• 401(k)