Job Description
Join NovoPharm Therapeutics, a leader in innovative pharmaceutical solutions, as a Senior Clinical Research Associate. You'll be pivotal in advancing groundbreaking therapies while ensuring compliance with global regulatory standards. This role offers hybrid work flexibility and opportunities to lead pivotal trials in oncology and immunology.
We foster a culture of scientific excellence and professional growth, with comprehensive benefits including stock options and continuing education stipends. Your work will directly impact patient outcomes and shape the future of medicine.
Responsibilities
- Oversee site management and monitoring for Phase II-III clinical trials across 10+ global sites
- Ensure protocol adherence and regulatory compliance (ICH-GCP, FDA, EMA)
- Lead vendor management and budget oversight for clinical operations
- Develop and execute risk-based monitoring strategies
- Coordinate cross-functional teams (data management, biostatistics, medical affairs)
- Mentor junior CRAs and contribute to process improvement initiatives
Qualifications
- Bachelor's degree in Life Sciences, Pharmacy, or related field (Master's preferred)
- 5+ years of clinical research experience with Phase II-III trials
- Certified Clinical Research Associate (CCRA) certification required
- Proven expertise in oncology/immunology therapeutic areas
- Advanced proficiency in eCRF systems (e.g., Medidata Rave)
- Exceptional problem-solving and cross-cultural communication skills
- Valid passport and willingness to travel 25-30%