Job Description
Join Novartis Pharmaceuticals as a Senior Clinical Research Associate and shape the future of healthcare innovation. We're seeking a dynamic professional to lead critical clinical trials, ensuring compliance with FDA and ICH guidelines while driving patient-centric research. This role offers unparalleled opportunities to collaborate with global teams, mentor junior staff, and contribute to breakthrough therapies that transform lives.
Responsibilities
- Design and execute Phase I-III clinical trials with precision and regulatory compliance
- Monitor investigator sites to ensure protocol adherence and data integrity
- Lead cross-functional teams to resolve complex operational challenges
- Analyze clinical data and prepare comprehensive regulatory submissions
- Mentor CRAs and implement process improvements for trial efficiency
- Represent company at investigator meetings and regulatory consultations
Qualifications
- Master's degree in Life Sciences, Pharmacy, or related field with 5+ years clinical research experience
- Certified CRA (ACRP/SoCRA) or equivalent professional certification
- Expertise in oncology or immunology therapeutic areas
- Proven track record in FDA/EMA regulatory compliance
- Advanced proficiency in EDC systems (e.g., Medidata Rave)
- Exceptional communication and stakeholder management skills
- Ability to travel 30% domestically/internationally