Lead Clinical Document Specialist

Clinical Research Associate RoleWe are seeking a skilled Clinical Research Associate to conduct clinical trial authoring and analysis tasks. As a key member of our team, you will be responsible for producing high-quality clinical documents.Key Responsibilities:Author and analyze clinical trial documents.Work with key clinical documents including protocol,...

Job Summary:We are seeking a highly skilled and detail-oriented Medical Document Reviewer to join our team. As a key member of our medical review process, you will be responsible for reviewing and assessing medical documents, including clinical trial data, safety reports, and regulatory submissions.

Job Title: Clinical Oversight LeadAbout the RoleThe Clinical Oversight Lead is responsible for ensuring effective clinical trial site monitoring activities. This role works closely with cross-functional teams to ensure Lilly has appropriate oversight of outsourced clinical trial site monitoring.Main Responsibilities:Conduct regular review of Monitoring Visit...

Job OpportunityWe are seeking a skilled professional to fill the role of Clinical Outreach Specialist. As a Clinical Outreach Specialist, you will play a vital part in engaging with communities and promoting our services.

Clinical Research AssociateJob Summary:We are seeking a Clinical Research Associate to support our clinical trial operations. The ideal candidate will have experience in authoring and analyzing clinical trial documents, working with key clinical documents, and collaborating with cross-functional teams.Main Responsibilities:Author and analyze clinical trial...

Job Title: Business Operations SpecialistSonata seeks an experienced professional with a deep understanding of business processes and stakeholder collaboration. The ideal candidate will have hands-on experience with clinical trial systems and have played a key role in 2-3 end-to-end technology implementations across the clinical trials value chain.The role...

Job DescriptionKey Accountabilities- Document Management:- Track, scan, code, and apply naming conventions to documents per the Central File Maintenance Plan (CFMP).- Archive and manage paper documents in the Central Files office.- Conduct photocopying, printing, distribution, and retrieval of documents as required.- Perform basic quality checks to ensure...

Job DescriptionA Coding Specialist I is a critical role in ensuring the accuracy and efficiency of medical coding data. The successful candidate will possess a solid understanding of medical coding processes and tools, as well as clinical trial processes including data management, clinical operations, and biometrics.The ideal candidate will have a minimum of...

Job Title: Clinical Data SpecialistAbout the Role:The Clinical Data Specialist plays a pivotal part in our organization by accurately coding medical records to facilitate efficient data indexing.This key position involves a range of activities, including but not limited to:Coding patient records with precision and speed.Ensuring compliance with established...

Job Summary: The Clinical Leader is responsible for overseeing the activities of clinical team members, ensuring high-quality patient care, and maintaining a safe and efficient work environment.Responsibilities:Coordinate and supervise clinical team members in providing patient care under the supervision of a Physician or provider.Organize and assign duties...