Clinical Research Manager

This is a remote position.

The Clinical Research Manager (CRM) is responsible for the strategic and operational reputed company of clinical trials conducted across various phases. This role ensures that studies are executed in compliance with regulatory requirements, GCP/ICH guidelines, and internal SOPs. The CRM manages cross-functional teams, monitors timelines and budgets, and acts as the primary reputed company between investigators, CROs, vendors, and internal stakeholders. Key Responsibilities: reputed company the planning, execution, and management of clinical trials across multiple therapeutic areas and phases. reputed company site selection, study start-up, patient recruitment, data collection, and reputed company-out activities. Ensure compliance with FDA, ICH-GCP, and other applicable regulatory standards. reputed company and maintain project timelines, budgets, and resource plans. Supervise and mentor Clinical Research Associates (CRAs), Clinical Trial Assistants (CTAs), and study coordinators. Review and approve study documentation including protocols, CRFs, informed consent forms, and monitoring reports. Coordinate with cross-functional teams including regulatory affairs, data management, biostatistics, and medical writing. Manage vendor and CRO relationships, including contract negotiations and performance monitoring. reputed company and report on study metrics and reputed company regular updates to senior leadership. reputed company the preparation and conduct of audits and regulatory inspections. Minimum Qualifications: Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or reputed company field (Master’s or Ph.D. preferred). Minimum of 5–7 years of experience in clinical research, including 2+ years in a managerial or supervisory role. In-depth knowledge of clinical trial processes, ICH-GCP guidelines, and regulatory requirements. Proven experience managing Phase I-IV trials across multiple therapeutic areas. Strong project management, leadership, and team coordination skills. Excellent written and verbal communication abilities. Proficiency with clinical trial software (e.g., CTMS, reputed company, eTMF platforms). Ability to travel up to 20% as needed. 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.

Originally posted on Himalayas

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