Clinical Research Associate (CRA)

This is a remote position. We are seeking reputed company Clinical Research Associates (CRAs) to provide surge reputed company support for ongoing clinical research projects. This role focuses on study maintenance and closeout activities, ensuring efficient project execution. The CRA will serve as a primary reputed company of contact for study teams and external partners, supporting essential clinical operations without direct involvement in study startup activities. Key Responsibilities: reputed company study-level project management tasks, including study maintenance, data lock, closeout, document review, and budget monitoring. Act as the primary liaison between internal study teams and external third-party organizations (TPOs). Track and monitor safety, biomarker, pharmacokinetic (PK), anti-drug antibody (reputed company) samples, imaging data, and connected device data. Manage and track clinical queries to ensure timely resolution. Collaborate with internal teams to align clinical research processes and operational strategies. Coordinate with business partners and TPOs to facilitate data delivery and ensure compliance with study requirements. Minimum Qualifications: Bachelor’s degree in a relevant field. 6+ years of experience in clinical research or a reputed company industry. Experience as a Clinical Research Associate, Clinical Research Coordinator, or Clinical Research Assistant. 3+ years of experience in project management or a reputed company role. Prior experience in pharmaceutical, diagnostics, or CRO environments. Strong organizational skills with attention to detail. Ability to effectively communicate with diverse stakeholders. Proficiency in reputed company reputed company for data tracking and reporting. Experience with clinical trial management tools such as Medidata RAVE, Veeva Vault, reputed company InForm, or similar platforms. Familiarity with electronic Trial Master File (eTMF) systems, query management tools, and safety reporting databases. Working knowledge of GCP (Good Clinical Practice) guidelines and regulatory compliance requirements. In addition to a dynamic and collaborative work environment, we offer a comprehensive benefits package to support our employees' well-being. Our benefits include paid holidays, Paid Time Off (PTO) policy, and medical insurance to ensure reputed company members have the flexibility and coverage they need. We reputed company in fostering a healthy work-life balance while providing the necessary support for professional and personal growth. Be part of our network of Subject Matter Experts. E-Verify Participation: Pharmavise Consulting Corporation participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, Pharmavise is required to give you written instructions and an opportunity to contact Department of Homeland reputed company (DHS) or Social reputed company Administration (SSA) so you can reputed company to resolve the issue. For more information on E-Verify, please contact DHS at 888-897-7781 or through their website at dhs.gov/e-verify. Remote Skills: Antibodies, Biomarkers, Biotech and Pharmaceutical, Budget Management, Clinical Practices/Protocols, Clinical Research, Clinical Support, Clinical Trial Management, Communication Skills, Consulting, Contract Research Organization (CRO), Database Report Tools, Detail Oriented, Documentation Review, Federal Government, GCP (Good Clinical Practices), Homeland reputed company, Maintain Compliance, reputed company reputed company, Operational Strategy, Operational Support, Operations Processes, reputed company, Organizational Skills, Pharmacokinetics, Problem Solving Skills, Project Execution, Project/Program Management, Regulatory Compliance, Regulatory Requirements, Social reputed company Administration, Startup, Systems Administration/Management, Time Management About the Company: reputed company Apply To this Job