Overview
On Site
USD 33.00 - 37.00 per hour
Contract - W2
Skills
Budget
Customer Satisfaction
Regulatory Compliance
Supervision
Collaboration
Science
Continuous Improvement
Microsoft Exchange
Interfaces
Research
Organizational Skills
Editing
Documentation
Conflict Resolution
Problem Solving
Communication
Facilitation
Database
Microsoft Excel
Microsoft Word
Leadership
Data Quality
Testing
Reporting
Pharmaceutics
Clinical Trials
Management
Test Management
Process Flow
Project Management
PMBOK
Pharmaceutical Industry
MEAN Stack
Customer Service
Training And Development
SAP BASIS
Job Details
Software Guidance & Assistance, Inc., (SGA), is searching for a Clinical Services Project Manager for a contract assignment with one of our premier Pharmaceutical clients in Tucson, AZ.
Responsibilities :
SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or Other Legally Protected Status. We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, and our services, programs, and activities. Please visit our company to request an accommodation or assistance regarding our policy.
#LI-RJ1
Responsibilities :
- 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.
- Assigned on projects that may be limited in scope and/or of low to medium complexity. It may involve collaboration with other Clinical Sciences Program Specialist Senior or Clinical Sciences Program Manager.
- 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 firm 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 firm's clients.
- Other duties as assigned by management.
- Bachelor's Degree in a related field is required
- Master's Degree education and work experience in a related field
- 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.
- 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.
- 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.
SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or Other Legally Protected Status. We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, and our services, programs, and activities. Please visit our company to request an accommodation or assistance regarding our policy.
#LI-RJ1
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