What are the responsibilities and job description for the Senior Clinical Research Scientist position at Hartmann Young?
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 (open to relocation support) and offers the opportunity to lead clinical programs and research projects that have global impact.
The Role
We are seeking an accomplished scientist with a strong background in clinical research, trial management, and manuscript development. This individual will oversee the start-up, execution, and close-out of clinical trials, while also contributing to product innovation, regulatory support, and publications. The position requires close collaboration with senior leadership to align research priorities with strategic growth initiatives.
Key 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.
Additional Details
- Full-time, on-site role. Full relocation support available.
- Requires willingness to travel for trial site visits, conferences, and client meetings.