Pharmavise Corporation
Biotechnology • Pharmaceuticals • Healthcare Insurance
Pharmavise Corporation is the first Continuous Compliance Organization (CCO) dedicated to maintaining the highest standards of quality and regulatory compliance in the life sciences industry. Our esteemed client base includes Fortune 500 companies in pharmaceuticals, medical devices, and biotechnology. We offer bespoke solutions tailored to meet the specific compliance needs of our clients, supporting them from development through commercialization and ensuring they exceed their compliance goals while enhancing patient health and safety.
Clinical Research Manager
Job not on LinkedIn
April 25
Pharmavise Corporation
Biotechnology • Pharmaceuticals • Healthcare Insurance
Pharmavise Corporation is the first Continuous Compliance Organization (CCO) dedicated to maintaining the highest standards of quality and regulatory compliance in the life sciences industry. Our esteemed client base includes Fortune 500 companies in pharmaceuticals, medical devices, and biotechnology. We offer bespoke solutions tailored to meet the specific compliance needs of our clients, supporting them from development through commercialization and ensuring they exceed their compliance goals while enhancing patient health and safety.
📋 Description
• This is a remote position • The Clinical Research Manager (CRM) is responsible for the strategic and operational oversight 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 liaison between investigators, CROs, vendors, and internal stakeholders • Lead the planning, execution, and management of clinical trials across multiple therapeutic areas and phases • Oversee site selection, study start-up, patient recruitment, data collection, and close-out activities • Ensure compliance with FDA, ICH-GCP, and other applicable regulatory standards • Develop 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 • Track and report on study metrics and provide regular updates to senior leadership • Oversee the preparation and conduct of audits and regulatory inspections
🎯 Requirements
• Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related 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, EDC, eTMF platforms) • Ability to travel up to 20% as needed
🏖️ Benefits
• paid holidays • Paid Time Off (PTO) policy • medical insurance
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