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Aviceda Therapeutics, a biotechnology company focusing on immune system modulation, seeks a Clinical Research Associate to advance clinical studies. Responsibilities include ensuring compliance with regulatory guidelines, collaborating with research teams, and managing clinical trials. The ideal candidate should have a Bachelor's degree in a science-based discipline, minimum 2 years of ophthalmology site management experience, and proficiency in Trial Master File and EDC systems. Knowledge of GCP and ICH guidelines, strong organizational and communication skills, and willingness to travel are essential. The position offers competitive compensation, employee benefits, and opportunities for professional growth in a dynamic environment.
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Seeking a Senior Statistical Programmer with advanced SAS programming skills
Join a supportive team in a data-focused clinical research organization
Posted 47 days ago
Deliver high-quality programming for clinical projects
Ensure compliance with industry and regulatory standards
Posted 73 days ago
Support strategic healthcare projects
Enhance market access and commercialization
Posted 73 days ago
Drive strategic growth and business development
Deliver high-quality advisory and consulting services
Posted 75 days ago
Deliver high-quality statistical programming for clinical studies.
Ensure compliance with clinical and regulatory standards.
Posted 91 days ago
Lead and manage CSV activities for clinical systems
Ensure compliance with regulatory guidelines (GxP, 21 CFR Part 11)
Posted 97 days ago
Develop high-quality scientific and medical content
Ensure compliance with regulatory and industry guidelines
Posted 165 days ago
Accelerate early-phase drug development
Offer flexible, client-focused research services
Posted 206 days ago
Advance innovative healthcare solutions
Focus on patient-first outcomes
Posted 209 days ago
Enhance global GxP training quality and compliance
Collaborate with teams to align learning solutions with business objectives
Posted 209 days ago
Develop and implement global GxP training models
Ensure compliance and quality in training programs
Posted 214 days ago
Advance pediatric cancer therapies
Innovate drug development processes
Posted 215 days ago
Deliver remote pediatric healthcare services
Support innovative medical research
Posted 236 days ago
Conduct site visits and monitor patient safety
Ensure protocol compliance and data accuracy
Posted 254 days ago
Oversee study and country level activities
Develop Recruitment Strategy
Posted 254 days ago
Lead statistical programming team
Provide high-quality service
Posted 272 days ago
Speeding life-changing medicines to market
Integrating patient insights and innovative trial designs
Posted 273 days ago
Transform data into research-ready datasets
Design and maintain data pipelines for healthcare data
Posted 276 days ago
Ensure clear and precise communication of critical medical information.
Collaborate with healthcare professionals and cross-functional teams.
