Clinical Study Associate Role

7 days ago


Tucson, Arizona, United States SGA Full time

About SGA

SGA is a technology and resource solutions provider driven to stand out. We are a women-owned business with a mission to solve big IT problems with a more personal, boutique approach.

We match consultants like you to over 1,000 engagements each year. Our team values customer service, employee development, and quality and integrity in everything we do.

Join us at https://sgainc.com/, where you can find our company's values and commitment to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment and services.

Clinical Study Associate Role Overview

This Clinical Study Associate role is a key position within the Clinical Services Management team, supporting the Clinical Services Project Management Team through various tasks linked to Sponsor's Monitoring Visits.

The ideal candidate will have strong communication skills, proficient in English language, both written and oral communications, and experience in administrative management, clinical research associate, or histo-technology laboratories.

This role requires excellent organizational skills, ability to multi-task, and a positive and energetic attitude.

You will be responsible for delivering specific tasks, generally overseen by the study Project and/or Program Managers, ensuring timely completion and maintaining quality standards.

Responsibilities

  • Support Clinical Services Project Management Team through Sponsor's Monitoring Visits
  • Day-to-day onsite administrative tasks to keep Sponsor's monitoring visits on track
  • Deliver specific tasks, generally overseen by study Project and/or Program Managers
  • Maintain quality standards and ensure timely completion of tasks
  • Work closely with Quality, firm CDx CAP/CLIA Laboratory, and Pathologist
  • Calendar Management: Coordinates with applicable functions times for SIV, Monitoring Visits, Closing Visits, and/or Audits times
  • Laboratory and/or Study Document Maintenance and Preparation for Auditors
  • Facilitate and/or attend Monitoring visits activities
  • Supplier Questionnaire Document Management
  • Participate in process improvement initiatives

Requirements

  • Bachelor degree preferably in life sciences, nursing or a related field of study; Business Administration or similar expertise through experience
  • 2+ years of administrative management, and/or entry level CRA (clinical research associate), CTA experience, or a history of working with histo-technology laboratories preferred but not required
  • Strong communication skills, proficient in English language, both written and oral communications; other languages desirable
  • Proficient in Microsoft Office (Word, Excel, PowerPoint) and Google Tools
  • Excellent organizational skills and ability to multi-task
  • Positive and energetic attitude
  • Able to take initiative, be adaptable, and strive in a dynamic environment
  • Strong attention to detail and commitment to delivering on time
  • Diligent and conscientious
  • Ability to work independently and as a team member
  • Possesses critical thinking and problem solving skills
  • Customer and Project Manager service oriented
  • Communicate effectively with various internal stakeholders in a positive and professional manner

Preferred Qualifications

  • Experience in cancer research
  • Have a working knowledge of ICH-GCP guidelines related to clinical trials
  • Worked in global locations

Estimated Salary: $60,000 - $80,000 per annum, depending on experience and qualifications.



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