Clinical Science Program Specialist

Tailored Management

Tucson, AZ(remote)

JOB DETAILS
SALARY
$35–$37 Per Hour
SKILLS
Best Practices, Biology, Biotech and Pharmaceutical, Clinical Data, Clinical Laboratory, Clinical Research, Clinical Trial, Clinical Trial Management, Communication Skills, Continuous Improvement, Contract Management, Contract Research Organization (CRO), Cross-Functional, Customer Relations, Customer/Client Research, Documentation, Editing, Health Plan, Laboratory Testing, Meeting Minutes, Organizational Skills, Pharmaceutical Data, Plan Meetings, Process Flow, Project Development, Project Planning, Project Tracking, Project/Program Management, Team Player, Test Lab, Time Management
LOCATION
Tucson, AZ
POSTED
2 days ago
Clinical Science Program Specialist
Location: Remote (organization is based in Tucson, AZ)
Pay Rate: $35-$37/hour, based on experience 
1 year contract with potential for extension and/or permanent placement
Weekly pay and healthcare benefits offered!


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 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 clients.
Qualifications 
  • 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.
#TMN

About the Company

T

Tailored Management

CONNECTING TOP TALENT WITH TOP-TIER OPPORTUNITIES

Tailored Management is a global staffing firm that specializes in partnering with large organizations that run their contingent labor program in a VMS/MSP environment. We have the unique capacity to support programs across all scopes and geographic locations from a single headquarters, successfully elevating program performance across the board and minimizing costs, miscommunication and delivery times. But what do we really do? We bring together the best talent with the greatest opportunities.

COMPANY SIZE
1,000 to 1,499 employees
INDUSTRY
Staffing/Employment Agencies
FOUNDED
1968
WEBSITE
https://www.tailoredmanagement.com/

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