
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.
🔥 0 minutes ago
Improve your chances of getting an interview by checking your resume score before you apply.

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 activities pertaining to Phase I–III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and relevant procedures and guidelines • 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 • Perform ongoing updates of Data Management-related documentation
• 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 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 • Must be based in Serbia
• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Reasonable accommodations, when appropriate
Apply Now🕒 July 15
Senior Pharmacovigilance Associate managing ICSR processing and client support at PrimeVigilance. Collaborating with global teams to ensure patient safety and compliance with regulations.
🕒 July 10
Senior Site Contract Associate at IQVIA Biotech handling contracting activities for clinical development across multiple studies and sponsors.
🕒 June 25
Senior Site Contracts Associate responsible for managing contract strategies and start-up activities for complex clinical studies at IQVIA Biotech across global biotech companies.