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).
...available during the following times:o 3am-10am EST (Monday to Friday) WHAT DO I NEED TO GET STARTED? Because youll be teaching online from your home, youll need your own computer and a good internet connection. All of our classes are conducted 1-on-1 via our...
...As a Store Manager Trainee, youll train on all aspects of successfully running a store in preparation for running for your own store. Youll be involved in supervising day-to-day store activities, ensuring overall store performance, identifying staffing needs, managing...
...radiologic films or other scans of various portions of the body to assist in the detection of foreign bodies and the diagnosis of... ...with childhood conditions. Work closely with team members of the Radiology Department and other collaborating departments throughout the hospital...
...joining the Siege team? We currently have a spot open for a talented Freelance Copy Editor to help us continue to deliver great content for... ...to detail with a heavy focus on AP style ~ Experience writing and editing for the web, with a focus on digital content including...
...about helping others and are eager to reach top-level leadership positions . If youre driven to make... ...opportunity is for you! Why Join Us?# Work from Home: Enjoy the freedom and flexibility of working remotely. Create your ideal workspace and balance both your...