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

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.
• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits • Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions • Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes • Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient • Demonstrates diligence in protecting the confidentiality of each subject/patient • Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations • Assesses site processes • Conducts Source Document Review of appropriate site source documents and medical records • Applies query resolution techniques remotely and on site • Utilizes available hardware and software to support the effective conduct of the clinical project data review and capture
• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements • Must demonstrate good computer skills and be able to embrace new technologies • Excellent communication, presentation and interpersonal skills • Ability to manage required travel of up to 75% on a regular basis
• 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
Apply Now🔥 10 hours ago
Clinical Trial Manager overseeing clinical trial operations at ICON to meet quality outcomes and compliance standards. Collaborating with teams to manage trials effectively.
🕒 June 9
501 - 1000
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Clinical Research Manager overseeing day-to-day clinical operations for ophthalmology studies in a fully remote setting. Join a global CRO partnering with biotech and pharmaceutical companies.
🗣️🇪🇸 Spanish Required
🗣️🇧🇷🇵🇹 Portuguese Required
🕒 April 7
Clinical Scientist managing clinical trial assessment for psychiatric evaluations. Collaborating with rater teams and ensuring standardized assessments in a multicultural environment.
🇦🇷 Argentina – Remote
💰 $1G Post-IPO Debt on 2023-05
⏰ Full Time
🟡 Mid-level
🟠 Senior
🧪 Clinical Research