Elevate your writing career as a Senior Clinical Scientist with Indero in Canada, contributing to high-quality clinical and regulatory documents. This role involves guiding study design and mentoring junior staff. Join a forward-thinking team at Indero, known for its expertise in dermatology and rheumatology. In this senior role, you'll apply your medical writing skills in developing clinical study protocols, reports, and analyses. Collaborate across functions to ensure timely project delivery while adhering to budget and SOP compliance. Key Responsibilities:
- Contribute to study design and clinical study protocols
- Write and review informed consent forms
- Analyze and interpret clinical study data
- Prepare scientific publications and abstracts
- Mentor junior team members on best practices
Requirements:
- MSc or relevant degree; PhD or MD preferred
- Minimum 6 years in clinical research; 3 in document writing
- Strong communication and medical writing skills
- Proficiency in Word, Excel, and PowerPoint
- In-depth knowledge of regulatory requirements in clinical trials
Leverage your expertise to impact clinical research at Indero as you support creative dermatological studies. #J-18808-Ljbffr