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
Direct impact on clinical strategy and regulatory success
Exposure to senior leadership and key scientific stakeholders
What You’ll Be Doing
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
About You
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
How To 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.
