Clinical Services Project Manager from Joulé
Oro Valley, AZ 85755
About the Job
Job Title: Clinical Services Project Manager
Location: Oro Valley, AZ
Hours/Schedule: M-F Business Hours
Pay Range: $33 - 37/hr
Type: Contract, Potential for extension or conversion to permanent
Overview
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.
Responsibilities
Requirements
Education Level
Experience:
Knowledge, Skill or Ability
Benefits
System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.
Location: Oro Valley, AZ
Hours/Schedule: M-F Business Hours
Pay Range: $33 - 37/hr
Type: Contract, Potential for extension or conversion to permanent
Overview
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.
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 company 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 company clients.
- Other duties as assigned by management.
Requirements
Education Level
- Bachelor's Degree in a related field is required
- Master's Degree education and work experience in a related field
- Specific Project Management Training, or Clinical Research training and/or certification.
Experience:
- Years of Experience: 2 years of project and/or clinical trial coordinator/management experience in a regulated, CRO, diagnostic, and/or pharmaceutical industry with regulated documentation
- Experience with clinical projects that require rapid activity/milestone achievement.
- Experience in clinical trial management and knowledge of bio-sample (clinical testing) management and process flow preferred.
- Previous experience with standard project management process (PMI) desired.
- Diagnostic and/or Pharmaceutical industry and relevant diagnostic area knowledge preferred.
Knowledge, Skill or Ability
- Possesses problem solving skills and ability to coordinate project related activities.
- Familiarity with management of Clinical Trials.
- Understanding of Quality and Regulatory processes.
- Knowledge of clinical sample process flow and testing.
- Strong Written and verbal communication skills and meeting facilitation skills.
- Proficiency with word processing, spreadsheet, database and email software (e.g., Microsoft Excel, Microsoft Word).
- Possesses interpersonal skills and ability to work in a team environment. Displays leadership skills.
- Ability to work under time pressure while maintaining high standards of precision and data quality.
- Ability to manage projects with activity/milestone achievement to complete clinical study testing and data reporting to pharma partners.
- Ability to apply specialized knowledge and skills in the functional areas, particularly interfacing with laboratory, scientific, and medical staff.
Benefits
System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.
Salary
33 - 37 /year