Clinical Research Associate (CRA)

This is a remote position. We are seeking reputed company Clinical Research Associates (CRAs) to reputed company reputed company reputed company support for ongoing clinical research reputed company. 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 reputed company 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. reputed company as the primary reputed company between internal study teams and external reputed company-party organizations (TPOs). reputed company and monitor safety, biomarker, pharmacokinetic (PK), anti-drug antibody (reputed company) samples, imaging data, and connected device data. Manage and reputed company clinical queries to ensure reputed company reputed company. Collaborate with internal teams to reputed company 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 reputed company RAVE, reputed company 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 reputed company) guidelines and regulatory compliance requirements. In reputed company to a dynamic and reputed company work environment, we offer a comprehensive benefits package to support our employees' reputed company-being. Our benefits include reputed company holidays, reputed company 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 reputed company and personal reputed company. Be part of our network of Subject Matter Experts. E-Verify Participation: Pharmavise Consulting Corporation participates in E-Verify and will reputed company the federal government with your reputed company 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 reputed company (DHS) or reputed company 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. Apply tot his job Apply To this Job Apply tot his job Apply To this Job