As Clinical Services Project Manager I, you will manage clinical and lab services projects from initiation through contract completion by applying project management skills and experience in delivering projects on time, within budget and with high customer satisfaction. You facilitate cross-functional interactions to complete the assigned projects within the deadline.
Your Opportunity
Managing clinical testing and lab services projects collaboratively, from initiation through contract completion.
Performing tactical coordination of timelines for all projects and functions within CDx Pharma Services such developing project plans, establishing and coordinating timelines for assigned projects and functions; managing execution of cross-functional plans and tracking the progress of activities; identifying gaps, potential bottlenecks or delays and challenge assumptions and propose options to close gaps
Oversees and guides day-to-day activities of sample process flow and accurate reporting of results. Implements 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.
Interface 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 Roche clients.
Completing miscellaneous duties and special projects as assigned.
This is a remote based role.
Who you are
You hold a Bachelor's Degree in a related field or equivalent combination of education and relevant work experience.
You bring 2 years experience of project and/or clinical trial coordinator/management experience in a regulated, CRO, diagnostic, and/or pharmaceutical industry with regulated documentation.
Preferred Requirements
You hold a Master's Degree in a related field and/or Specific Project Management Training, or Clinical Research training and/or certification.
Your experience is in clinical trial management and knowledge of bio-sample (clinical testing) management and process flow in the Diagnostic and/or Pharmaceutical industry.
Previous experience with standard project management process (PMI).
Behaviors, competencies, and qualities of the ideal Clinical Services Project Manager I
Understanding of Quality and Regulatory processes.
Knowledge of clinical sample process flow and testing.
Proficiency with word processing, spreadsheet, database, and email software (e.g., Microsoft Excel, Microsoft Word).
Ability to apply specialized knowledge and skills in functional areas, particularly interfacing with laboratory, scientific and medical staff.
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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Your Opportunity
Managing clinical testing and lab services projects collaboratively, from initiation through contract completion.
Performing tactical coordination of timelines for all projects and functions within CDx Pharma Services such developing project plans, establishing and coordinating timelines for assigned projects and functions; managing execution of cross-functional plans and tracking the progress of activities; identifying gaps, potential bottlenecks or delays and challenge assumptions and propose options to close gaps
Oversees and guides day-to-day activities of sample process flow and accurate reporting of results. Implements 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.
Interface 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 Roche clients.
Completing miscellaneous duties and special projects as assigned.
This is a remote based role.
Who you are
You hold a Bachelor's Degree in a related field or equivalent combination of education and relevant work experience.
You bring 2 years experience of project and/or clinical trial coordinator/management experience in a regulated, CRO, diagnostic, and/or pharmaceutical industry with regulated documentation.
Preferred Requirements
You hold a Master's Degree in a related field and/or Specific Project Management Training, or Clinical Research training and/or certification.
Your experience is in clinical trial management and knowledge of bio-sample (clinical testing) management and process flow in the Diagnostic and/or Pharmaceutical industry.
Previous experience with standard project management process (PMI).
Behaviors, competencies, and qualities of the ideal Clinical Services Project Manager I
Understanding of Quality and Regulatory processes.
Knowledge of clinical sample process flow and testing.
Proficiency with word processing, spreadsheet, database, and email software (e.g., Microsoft Excel, Microsoft Word).
Ability to apply specialized knowledge and skills in functional areas, particularly interfacing with laboratory, scientific and medical staff.
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.