
10,000+ employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.
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10,000+ employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.
• Perform ongoing data review • Reconcile third-party data streams • Reconcile serious adverse events with the safety database • Perform User Acceptance Testing (UAT) of clinical databases • Perform Quality Control (QC) of clinical databases • Update Data Management-related documentation as needed • Meet timelines and deliverables • Collaborate with sponsor-dedicated Data Management and Biostatistics teams for a global biopharmaceutical company
• Bachelor's degree OR certification in a related allied health profession from an appropriately accredited institution (i.e. RN, MT, PA, RT) is preferred, but individuals with commensurate experience will be considered • Minimum of 2 years of data management experience in Pharma or Clinical Research area is required • Experience with Electronic Data Capture (EDC) system(s) is required • Experience with Oracle Inc.'s Inform™ EDC system is preferred • Oncology and/or inflammatory therapeutic area experience is preferred • Conduct Phase I-III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and relevant procedures and guidelines
• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition program • Total rewards program • Inclusive culture • Comprehensive resources including emerging technologies, data, science and knowledge sharing • Therapeutically or functionally aligned expert collaboration • Specialized team collaboration
Apply Now🕒 July 14
Senior Site Contract Associate working with biotech firms on clinical trial contracting. Leading operational support and ensuring regulatory compliance in multicountry projects.