
10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
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
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
• Enter information into PVG quality and tracking systems for receipt and tracking ICSR as required. • Assists in the processing of ICSRs according to Standard Operating Procedures (SOPs) and project/program-specific safety plans as required. • Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability. • Codes events, medical history, concomitant medications, and tests. Compiles complete narrative summaries. • Identifies information to be queried and follows up until information is obtained and queries are satisfactorily resolved. • Assists in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements. • Maintains safety tracking for assigned activities. • Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, MedDRA coding as required.
• Bachelor’s Degree in life science, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills, and abilities to perform the job. • Safety Database systems and knowledge of medical terminology required. • Good understanding of clinical trial process across Phases II-IV and/or post-marketing safety requirements, ICH GCP, GVP and regulations related to Safety and Pharmacovigilance. • Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), Visio, email (Outlook), Team Share (or another management/shared content/workspace) and internet. • Excellent communication and interpersonal skills, both written and spoken. • Good organizational skills with proven ability to prioritize and work on multiple tasks and projects. • Detail oriented with a high degree of accuracy and ability to meet deadlines.
• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. • We are committed to building an inclusive culture – where you can authentically be yourself.
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