Clinical Project Manager

Key responsibilities

• Monitor and report on the progress of delegated clinical trials, which includes budgets and timelines
• Prepare, oversee, and review documents that are related to assigned clinical study
• Review and approve invoices being presented by study vendors and external consultants
• Oversight and management of CRO
• Help in the training and development of clinical staff as at when due
• Lead the clinical project team and various study team meetings
• Oversee the pattern and manner in which clinical research study is being conducted
• Fully involved in resolving issues; take part in procedure improvement initiatives
• Attain clinical study’s goals by working with other members of the study team to outline their priorities, and to also resolve conflicts that may come up in the project process
• Work together with clinical trial managers and document control personnel to manage documents that are related to the clinical study.

Your profile

• Must possess excellent communication skills so as to be able to effectively convey messages across to both study team members and other external persons like vendors and external consultants
• Good problem-solving, organizational, and leadership skills are highly required
• Ability to work with little or no supervision
• Ability to pay attention to detail at all times
• Must be able to work within stipulated timeframes or deadlines even in the face of multiple responsibilities or projects
• Must be able to work as part of a team or in most cases lead a team
• Must have a ‘one of a kind’ work ethic, and must exhibit a great level of self-discipline
• Ability to organize and motivate other members of the study team
• A Bachelor’s and/or a Master’s degree in any science or health-related field
• A minimum of 12 years experience in the field of clinical research of which 5 years must have been in a project lead role
• Proficient user of MS Office applications for the execution of daily project operations