Position : Clinical Project Manager
Working Hours: Â US Working hours - EST
Salary Range:Â $3,000 - $4,500 Usd Based on experience
Type of Contract : Independent Contractor Agreement
The Clinical Project Manager (CPM) is responsible for the overall coordination, implementation, execution, and delivery of clinical trials within timelines, budget, and scope. Working within a Contract Research Organization (CRO) environment, the CPM ensures that all clinical project activities are conducted in accordance with applicable regulatory guidelines, client expectations, and standard operating procedures (SOPs).
Lead and manage the planning and execution of clinical trials from initiation through close-out.
Serve as the primary point of contact for clients and internal teams, ensuring alignment and communication throughout the project lifecycle.
Develop project plans, timelines, and budgets; track progress and report status to stakeholders.
Coordinate and oversee cross-functional project teams, including clinical monitors, data management, biostatistics, regulatory affairs, and medical writing.
Identify potential project risks and develop mitigation strategies.
Ensure compliance with ICH-GCP, regulatory requirements, SOPs, and client specifications.
Oversee site selection, initiation, monitoring, and closeout activities in collaboration with clinical operations staff.
Maintain and manage trial master files and ensure proper documentation.
Provide leadership, mentoring, and training to project team members as needed.
Participate in proposal development and bid defense meetings when required.
Minimum of 4â6Â years of experience in clinical research, with at least 2 years in a project management role within a CRO or pharmaceutical company.
Strong knowledge of ICH-GCP and global regulatory requirements.
Demonstrated ability to manage multiple projects simultaneously.
Excellent organizational, leadership, and communication skills.
Proficiency in project management tools and MS Office Suite.
Ability to travel as needed (domestic and international).
PMP certification or equivalent is a plus.
Experience in specific therapeutic areas (e.g., oncology, CNS, cardiology) is an advantage.
Familiarity with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
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