Clinical Science Program Specialist
Nesco Resource ·nescoresource.com
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The Opportunity
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 Roche 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.
Requirements
At least 2 years of project and/or clinical trial coordinator/management experience in a regulated, CRO, diagnostic, and/or pharmaceutical industry with regulated documentation
Exposure to clinical studies
Experience with clinical projects that require rapid activity/milestone achievement.
Strong communication, collaboration, and organizational skills are required
Bachelor's degree is required (Life Sciences is preferred)
Preferred
Previous experience with standard project management process (PMI) desired.
Experience in clinical trial management and knowledge of bio-sample (clinical testing) management and process flow preferred.
Preferred experience in clinical studies or companion diagnostics
Diagnostic and/or Pharmaceutical industry and relevant diagnostic area knowledge preferred.
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.
#EDS014
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 Roche 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.
Requirements
At least 2 years of project and/or clinical trial coordinator/management experience in a regulated, CRO, diagnostic, and/or pharmaceutical industry with regulated documentation
Exposure to clinical studies
Experience with clinical projects that require rapid activity/milestone achievement.
Strong communication, collaboration, and organizational skills are required
Bachelor's degree is required (Life Sciences is preferred)
Preferred
Previous experience with standard project management process (PMI) desired.
Experience in clinical trial management and knowledge of bio-sample (clinical testing) management and process flow preferred.
Preferred experience in clinical studies or companion diagnostics
Diagnostic and/or Pharmaceutical industry and relevant diagnostic area knowledge preferred.
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.
#EDS014
Frequently asked questions
Who is hiring for the Clinical Science Program Specialist role?
Nesco Resource is hiring for the Clinical Science Program Specialist position, a Shazamme client. Apply directly on the employer's career site.
Where is the Clinical Science Program Specialist job located?
The Clinical Science Program Specialist role with Nesco Resource is based in Tucson, AZ, US.
What does the Clinical Science Program Specialist role pay?
Nesco Resource lists the Clinical Science Program Specialist role at USD 30–35 per hour.
Is the Clinical Science Program Specialist role full-time or contract?
This is a full time position at Nesco Resource.
What experience level is the Clinical Science Program Specialist role?
The Clinical Science Program Specialist position is aimed at mid-level candidates.
How do I apply for the Clinical Science Program Specialist role at Nesco Resource?
Apply directly on Nesco Resource's career page via the Apply button on this listing. ZammeJobs links straight through to the employer's ATS — no third-party form, no resume database.