What are the responsibilities and job description for the Sr Clinical Scientist position at Scientific Search?
Senior Clinical Scientist
Location: Raleigh, NC
6 Month Contract
Step into a high-impact role where your scientific insight directly shapes the future of aesthetic medicine. As a key contributor within a global R&D team, you’ll help design and deliver innovative clinical programs that bring cutting-edge products and indications to market. This is your opportunity to influence strategy, data, and outcomes on a global scale.
Why You Should Apply
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to ava@scientificsearch.com and tell me why you’re interested. Or, feel free to email your resume. Please include Job#19847.
Location: Raleigh, NC
6 Month Contract
Step into a high-impact role where your scientific insight directly shapes the future of aesthetic medicine. As a key contributor within a global R&D team, you’ll help design and deliver innovative clinical programs that bring cutting-edge products and indications to market. This is your opportunity to influence strategy, data, and outcomes on a global scale.
Why You Should Apply
- Competitive contract role with strong potential for permanent conversion
- Work on breakthrough aesthetic products across devices, drugs, and biologics
- Highly collaborative, global, cross-functional environment
- Direct impact on clinical strategy and regulatory success
- Exposure to senior leadership and key scientific stakeholders
- Contribute scientific expertise to clinical trial design, execution, and strategy
- Analyze and interpret clinical and preclinical data to guide development
- Author and review key clinical and regulatory documents
- Collaborate with global teams to drive study progress and outcomes
- Support regulatory submissions and publication of clinical results
- Oversee external medical writing vendors and ensure quality deliverables
- MSc in Life Sciences (PhD, MD, or DrPH preferred)
- Strong knowledge of clinical development and trial processes
- Familiarity with FDA/EMA regulations, GCP, ICH, or ISO guidelines
- Exceptional scientific writing and data interpretation skills
- Ability to manage multiple priorities in a fast-paced environment
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to ava@scientificsearch.com and tell me why you’re interested. Or, feel free to email your resume. Please include Job#19847.