Clinical Science Program Specialist

LanceSoft Inc

Tucson, AZ

JOB DETAILS
SALARY
$37–$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 Research Organization (CRO), Cross-Functional, Customer Relations, Documentation, Editing, 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
3 days ago
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 *** 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.

About the Company

L

LanceSoft Inc

We are a $125 Million, NMSDC-certified Minority & Woman owned Workforce Solutions Company headquartered in the DC metro area with presence across US with global presence - Canada, Mexico, India, UK, Malaysia, Indonasia, Hongkong, Singapore, UAE. We are specialized in providing Workforce Solutions, SOW project delivery, Engineering Solutions, Creative Services. We currently support 100+ Fortune companies globally and across multiple industry segments. We are currently supporting several massive programs across industry segment nationally/globally (Intel, Ally, AMD, QUALCOMM, Morgan Stanley, Kraft/ Mondelez, MNP, Amdocs, Dell, SanDisk, Medtronic, Becton Dickinson, GE, Lockheed Martin, UTC, L-3 Communications, Caterpillar, BMW, Mercedes Benz, National Grid, Dominion, Energy Future Holdings, PSEG, 3M, Fidelity, Aetna, Humana, Johnson & Johnson, Pfizer, Merck etc). 

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, identity, national origin, disability, or protected veteran status.

COMPANY SIZE
2,000 to 2,499 employees
INDUSTRY
Staffing/Employment Agencies
FOUNDED
2000
WEBSITE
http://www.lancesoft.com/

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