Clinical Service Project Manager I - RTD
Location: Tucson, OFF-CAMPUS
Shift: 1st
Schedule: Mon - Fri
JOB SUMMARY
Under general supervision, manages multiple clinical and lab services projects of less complex nature from initiation through contract completion. Applies project management skills and experience in delivering projects on time, within budget and with high customer satisfaction. Facilitates cross-functional interactions to complete the assigned projects within the deadline and compliance with pharma services plan.
DISTINGUISHING CHARACTERISTICS:
This job is the first in the Clinical Sciences project management job series comprising four levels. The employee is assigned on projects that may be limited in scope and/or of low to medium complexity. It may involve collaboration with other Clinical Services Project Managers or Clinical Services Program Manager.
Responsibilities
• Manages multiple clinical testing and lab services projects from initiation through contract completion under supervision of Program Manager. Acts as primary point of contact to Pharma customers.
• Performs tactical coordination of timelines for all projects and functions within CDx Pharma Services and:
- Develops project plans, establish and coordinates timelines for assigned projects and functions;
- Manages execution of cross-functional plans and tracks progress of activities;
- Identifies gaps, potential bottlenecks or delays, and challenge assumptions.
• Oversees and guides day-to-day activities of sample process flow and accurate reporting of results. Implements / pulls in best practices within the clinical sciences team; fosters continuous improvement by ensuring knowledge and experience exchange
• Guides and manages cross-functional interactions to complete the assigned projects within the deadline.
• Interfaces with resources outside of the company (Contract Research Organizations (CROs), site investigators, client counterparts, etc.) and serves as single point of contact with Pharma and clients.
• Manages meeting activities such as setting agendas, organizing meeting time, and editing meeting minutes.
• Tracks, maintains and communicates project reports and clinical study data to Pharma and clients.
• Other duties as assigned by management.
Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.
Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
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Location: Tucson, OFF-CAMPUS
Shift: 1st
Schedule: Mon - Fri
JOB SUMMARY
Under general supervision, manages multiple clinical and lab services projects of less complex nature from initiation through contract completion. Applies project management skills and experience in delivering projects on time, within budget and with high customer satisfaction. Facilitates cross-functional interactions to complete the assigned projects within the deadline and compliance with pharma services plan.
DISTINGUISHING CHARACTERISTICS:
This job is the first in the Clinical Sciences project management job series comprising four levels. The employee is assigned on projects that may be limited in scope and/or of low to medium complexity. It may involve collaboration with other Clinical Services Project Managers or Clinical Services Program Manager.
Responsibilities
• Manages multiple clinical testing and lab services projects from initiation through contract completion under supervision of Program Manager. Acts as primary point of contact to Pharma customers.
• Performs tactical coordination of timelines for all projects and functions within CDx Pharma Services and:
- Develops project plans, establish and coordinates timelines for assigned projects and functions;
- Manages execution of cross-functional plans and tracks progress of activities;
- Identifies gaps, potential bottlenecks or delays, and challenge assumptions.
• Oversees and guides day-to-day activities of sample process flow and accurate reporting of results. Implements / pulls in best practices within the clinical sciences team; fosters continuous improvement by ensuring knowledge and experience exchange
• Guides and manages cross-functional interactions to complete the assigned projects within the deadline.
• Interfaces with resources outside of the company (Contract Research Organizations (CROs), site investigators, client counterparts, etc.) and serves as single point of contact with Pharma and clients.
• Manages meeting activities such as setting agendas, organizing meeting time, and editing meeting minutes.
• Tracks, maintains and communicates project reports and clinical study data to Pharma and clients.
• Other duties as assigned by management.
Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.
Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.