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Clinical Science Program Specialist

Software Guidance & Assistance

Tucson, AZ(remote)

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JOB DETAILS
SALARY
$35–$35 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 Support/Service, Documentation, Editing, Genetics, Laboratory Testing, Meeting Minutes, Organizational Skills, Pharmaceutical Data, Plan Meetings, Problem Solving Skills, Process Flow, Project Development, Project Planning, Project Tracking, Project/Program Management, Staff Development, Team Player, Test Lab, Time Management
LOCATION
Tucson, AZ(remote)
POSTED
1 day ago
Software Guidance & Assistance, Inc., (SGA), is searching for a Clinical Science Program Specialist for a contract assignment with one of our premier Pharmaceutical clients in Tucson, AZ.

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 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 Pharma and firm clients.
Required Skills:
  • Bachelor's degree is required (Life Sciences is preferred)
  • 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
Preferred Skills:
  • 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.
SGA is a technology and resource solutions provider driven to stand out. We are a women-owned business. Our mission: to solve big IT problems with a more personal, boutique approach. Each year, we match consultants like you to more than 1,000 engagements. When we say let's work better together, we mean it. You'll join a diverse team built on these core values: customer service, employee development, and quality and integrity in everything we do. Be yourself, love what you do and find your passion at work. Please find us at https://sgainc.com/ .

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 EEO page to request an accommodation or assistance regarding our policy

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Software Guidance & Assistance

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