[Hiring] Senior Client Project Manager @Exelead Inc., USA
Role Description
The employee is responsible for effective planning, development, and execution of work plans for programs as measured by the ability to meet agreed upon milestones, budgetary constraints, and scope. The Senior Project Manager will support key clients and organize programs and activities in accordance with the mission and goals of the company. The incumbent will support special programs and projects as specified by the executive leadership team.
• Manage the operational aspects of the site's most critical projects and programs, including, but not limited to: scope, schedule, cost, earned value, quality, communications, risk, and change.
• Carry out coordinated organization, direction and implementation of projects and programs and transform activities to achieve outcomes and realize benefits of strategic importance to the business.
• Key Project Management resource for internal and external communication with significant clients; chairing formal tactical meetings and appropriate Senior Management steering committees.
Qualifications
• 5-7+ years experience in Project Management within the pharmaceutical industry, or foundational experience within the pharmaceutical industry in QA, QC, Engineering, Scientific, Commercial, Manufacturing or related functions.
• Solid proficiency in program and project management methodologies.
• Experience writing project proposals and service agreements.
Requirements
• Project Management certification (PMP®) or Program Management certification (PgMP®).
• Portfolio management experience.
• Understanding of drug development, regulatory, QA, and CMC processes, and clinical trials operations.
• Role can be based anywhere in the US.
Benefits
• Pay Range for this position: $97,200- $170,200.
• The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors.
• Position may be eligible for sales or performance-based bonuses.
• Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites.
Company Description
We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
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The employee is responsible for effective planning, development, and execution of work plans for programs as measured by the ability to meet agreed upon milestones, budgetary constraints, and scope. The Senior Project Manager will support key clients and organize programs and activities in accordance with the mission and goals of the company. The incumbent will support special programs and projects as specified by the executive leadership team.
• Manage the operational aspects of the site's most critical projects and programs, including, but not limited to: scope, schedule, cost, earned value, quality, communications, risk, and change.
• Carry out coordinated organization, direction and implementation of projects and programs and transform activities to achieve outcomes and realize benefits of strategic importance to the business.
• Key Project Management resource for internal and external communication with significant clients; chairing formal tactical meetings and appropriate Senior Management steering committees.
Qualifications
• 5-7+ years experience in Project Management within the pharmaceutical industry, or foundational experience within the pharmaceutical industry in QA, QC, Engineering, Scientific, Commercial, Manufacturing or related functions.
• Solid proficiency in program and project management methodologies.
• Experience writing project proposals and service agreements.
Requirements
• Project Management certification (PMP®) or Program Management certification (PgMP®).
• Portfolio management experience.
• Understanding of drug development, regulatory, QA, and CMC processes, and clinical trials operations.
• Role can be based anywhere in the US.
Benefits
• Pay Range for this position: $97,200- $170,200.
• The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors.
• Position may be eligible for sales or performance-based bonuses.
• Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites.
Company Description
We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply tot his job
Apply To this Job