Sr Clinical Scientist (Remote Contract)
Senior Clinical Scientist (Remote)
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
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 [email protected] and tell me why you’re interested. Or, feel free to email your resume. Please include Job#19847.
Apply tot his job
Apply To this Job
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
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 [email protected] and tell me why you’re interested. Or, feel free to email your resume. Please include Job#19847.
Apply tot his job
Apply To this Job