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Interactive Response Technology (IRT) systems and solutions provider supporting the life sciences industry.
Associate Project Manager
Location
United States
Posted
112 days ago
Salary
$69K - $79K / year
Seniority
Mid Level
Job Description
Associate Project Manager
Endpoint Clinical
• Lead projects of low to moderate complexity with support from senior team members • Act as primary point of contact for clients, keeping them apprised of all project developments while maintaining stellar client satisfaction • Build effective partnerships with other internal teams to move project through all phases of the development process. • Develop and maintain project schedule, identify and track milestones and identify and manage cross-functional dependencies and risks • Act as subject matter expert on client clinical study protocol • Manage ongoing reporting of project health and profitability to internal and external stakeholders. • Conduct end- user training • Manage issue resolution for studies in maintenance, including troubleshooting
Job Requirements
- Bachelor's degree or equivalent and/or appropriate experience
- 1-2 years’ experience in client-facing, project support role(s), including job responsibilities similar to those described above
- 1-2 years’ experience in life sciences industry
- Familiarity using SQL a plus
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• Lead clinical projects in accordance with the study budget and scope of work • Serve as the primary point-of-contact liaison with the client to provide excellent customer service • Liaise with Project Team and senior management of both Precision and sponsors • Handle and lead all aspects of a clinical research trial or trials • Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics • Prepare project status updates for clients and management • Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials • Prepare and review protocols and other study documentation such as project plans, inform consents, site contracts and budgets
• Independently lead clinical projects in accordance with the study budget and scope of work. • Use your strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects; both contracted objectives and financial objectives. • Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations. • Liaise with Project Team and senior management of both Precision and sponsors, including C level. • Handle and lead all aspects of a clinical research trial or trials. • Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc. • Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation. • Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials. • Prepare and reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgets.
• In this pivotal role you will have full service oversight for clinical projects across global/regional (ph I-IV) trials, within Oncology (or Rare Diseases or CNS). • Accountable for clinical project delivery, oversight of all functional departments, and ensuring agreed timelines, scope, cost and quality. • Involved in all study stages, including proposal strategy, development, costing, and bid defence, and seeing studies through the full cycle to completion, managing the client relationship, project team and budget and timelines throughout. • You will work in a cross-functional team with both internal and external stakeholders, driving quality and coordinating the study team. • You will independently lead clinical projects in accordance with the study budget and scope of work. You will use your strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects; both contracted objectives and financial objectives. You may be called upon to run international trials as well. • Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations. • Liaise with Project Team and senior management of both Precision and sponsors, including C level. • Handle and lead all aspects of a clinical research trial or trials. • Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc. • Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation. • Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials. • Prepare and review protocols and other study documentation such as project plans, inform consents, site contracts and budgets.

