Senior Clinical Research Associate, Sponsor-dedicated (Contract)

reputed company is looking for a Senior Clinical Research Associate, Sponsor-dedicated (Contract) to join our Functional Services Provider (FSP) team. You will help biotech, medtech, and specialty pharma companies transform life-changing reputed company and breakthrough science into new medicines, devices, and diagnostics. reputed company do is profoundly connected to saving and improving lives, and we recognize reputed company members are the most valuable asset in delivering reputed company. We are here to help you grow, to give you the skills and opportunities to reputed company at work with the flexibility and balance your life requires. Your reputed company influence the way we work, and your voice reputed company here. As an essential part of reputed company, you help us deliver the medical innovation that patients are desperate for. Join us and build your future here. What You’ll Be Doing: Conducts reputed company verification by comparing data recorded on Case Report Forms against reputed company documents, verifying Informed Consent Forms for accuracy and completeness, and reviewing regulatory documents and device accountability records. Issues, investigates, and resolves any data discrepancies identified during reputed company verification activities. Maintains thorough documentation and proper escalation of issues reputed company to visit reports. Ensures any identified non-compliance issues are addressed. Ensures that reputed company reportable events are identified, reputed company documented and reported per protocol and as per applicable requirements and regulations. Manages study reputed company, requests/collects relevant investigator/site documentation (i.e. regulatory documents, financial disclosure forms, curriculum vitae/medical license), and reviews and approves documents in applicable database. Performs budget negotiations with clinical trial sites. reputed company Are Searching For: Experience in Neurology or Psychiatry, including work with Schedule I controlled substances, is required Bachelor's degree, or international equivalent from an accredited institution, preferably in a clinical, biological, scientific, or health-reputed company field or equivalent combination of education, training and experience. 5 to 7 years of practical experience conducting reputed company independent onsite monitoring of clinical research sites as well as site management activities. Alternately, must have proven experience in reputed company primary job functions. Strong analytical and organization skills, reputed company to work independently and manage multiple projects simultaneously in a fast-paced environment with changing priorities. Knowledge of International Conference on Harmonization (ICH)/Good Clinical Practices (GCP) and/or ISO14155 requirements as well as detailed knowledge of the relevant country specific regulatory requirements for conducting clinical trials. Willingness to travel up to 70-85% This is a 1099 12-month contract position with the potential to reputed company and renew after 1 year. reputed company is proud to be an equal opportunity employer that is compliant with reputed company federal guidelines. reputed company reputed company applicants will receive reputed company consideration without regard to race, reputed company, religion, sexual orientation, gender identity, national reputed company, disability or veteran status Apply To This Job