Job Description

If you are an experienced Clinical Research Associate who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!

Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.

TRIO is looking for a CRAto join our Monitoring Resources team in the USA. This position will be remote, based out of the West Coast, and will require travel.

Responsibilities:

• Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local
  regulatory requirements, TRIO Standard Operating Procedures (SOPs), Standard
  Guidelines (SGs), Instruction Manuals (IMs), study protocols and study-specific SGs/IMs,
  for multiple projects
• Conduct Pre-Study Site Visits (or calls), Study Initiation Visits, Routine Monitoring Visits
  and Site Close-out at assigned clinical study sites as per TRIO SOPs/SGs/IMs and study-
  specific SGs/IMs
• Perform source document verification, validate Case Report Forms (CRFs) and perform
  query resolution in a timely manner to ensure clean data availability for studies
  analyses
• Input and maintain study information in tracking systems: Provide regular/accurate sites
  status updates and common site trends to Monitoring Resources and Project
  Management Departments
• Oversee study drug management at clinical study sites (availability, receipt, handling,
  storage, dispensation, tracking and accountability, and destruction/return)
• Perform Investigator Study File reconciliation: request any new or updated site-related
  essential documents and review them for content, consistency with other documents,
  and compliance with local regulatory requirements, ICH-GCPs guidelines, SOPs
• Respond to requests from clinical study sites in a timely fashion
• Establish and maintain good rapport with clinical study sites

Qualifications:

• At least 2 years of oncology experience as CRA, Coordinator, and/or research nurse.
• Bachelor's Degree in allied health fields such as Medical, Nursing, Pharmacy, or Health
  Science - or its international equivalent
• Local regulatory requirements knowledge would be a major asset
• At least one year of experience on an early phase trial
• Expereince with Breast, Lung, Gastric, and/or Ovarian Tumors would be a major asset
• Good knowledge of medical terminology and clinical monitoring process
• Strong ICH-GCPs knowledge
• Ability to prioritize multiple tasks and achieve project timelines
• Effective time management in order to meet daily metrics or team objectives
• Experience using computerized information systems, electronic spreadsheets, word
  processing and electronic mail
• Ability to travel up to 60% on average

What TRIO Can Offer You:

• Competitive Salary
• 3 weeks of vacation plus paid Christmas Closure
• 2 weeks paid personal/sick time
• 100% health benefits for you and your family paid by TRIO
• Flexible working hours
• Monthly internet allowance
• 401K Program 5% Salary Contribution
• Home office allowance
• Luggage allowance

Pay Range: $112,000 - $146,000. Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data.

Prior to applying please review TRIO's Applicant Information Notice

To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI.

To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI-generated responses during interviews or assessments. We want the opportunity to get to know you and your experience.

Teamwork • Passion • Integrity • Innovation

Job Tags

Full time, Local area, Remote work, Home office, Flexible hours

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