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Research Tech I

2+ years
Not Disclosed
10 Oct. 22, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Research Technician – Clinical Pharmacology Start-Up Team

Company: Fortrea

As a leading global contract research organization (CRO) with a commitment to scientific rigor and decades of clinical development experience, Fortrea provides comprehensive solutions across more than 20 therapeutic areas to pharmaceutical, biotechnology, and medical device customers. With operations in over 90 countries, we are transforming drug and device development for partners and patients worldwide.

We are currently seeking a Research Technician to join our Clinical Pharmacology Start-up team in Dayton Beach. In this full-time, office-based role, you will play a crucial part in initiating Early Phase clinical trials with maximum speed and efficiency.

Why Join Us?

Working in Phase 1 trials allows you to have a direct impact on patient care. You will establish the safety, tolerability, and pharmacokinetics of new drugs while maintaining close relationships with study participants. You'll have the opportunity to practice your clinical skills, engage with the latest medical technologies, and witness the development of groundbreaking treatments. Knowing that the drug you helped with may improve countless lives worldwide is incredibly rewarding.

Key Responsibilities

  • Provide high-quality care for participants in clinical trials and respond to emergencies based on clinical research standards.
  • Perform vital sign assessments, including blood pressure, venipuncture, weight, pulse, respiratory rate, and temperature readings.
  • Assist with screening procedures and maintain a clean and efficient study environment.
  • Foster respectful relationships with study participants and accurately record all research data.
  • Conduct quality control of source documents and case report forms while maintaining knowledge of regulatory requirements.
  • Attend required meetings and assist with study procedures as needed.
  • Maintain participant safety, dignity, and confidentiality at all times.

Benefits

Full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits, including:

  • Medical, Dental, Vision, and Life Insurance
  • Short-Term and Long-Term Disability Coverage
  • 401(K) Retirement Plan
  • Paid Time Off (PTO)
  • Employee Recognition Awards
  • Multiple Employee Resource Groups (ERGs)

Qualifications

  • High School Diploma or equivalent; EMT, Phlebotomy, CMA, or CNA certification preferred.
  • An Associate’s degree in a related field or 1 year of clinical research experience may substitute for a Bachelor’s degree.
  • Previous clinical experience is ideal but not required; we welcome recent graduates and those with relevant clinical experience.

Work Environment

You should be comfortable in a fast-paced environment where adherence to study protocols is crucial, and priorities may shift frequently. Strong teamwork and people skills are essential, as we utilize technology to collect data directly in an electronic environment.

Join Us!

At Fortrea, we seek motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Join our exceptional team and embrace a collaborative workspace that nurtures personal growth and enables you to make a meaningful global impact.

For more information about Fortrea, visit www.fortrea.com.

Fortrea is an Equal Opportunity Employer:

As an EOE/AA employer, we are committed to diversity and inclusion in the workforce and do not tolerate any form of discrimination. We encourage all qualified candidates to apply.

For information about how we collect and store your personal data, please see our Privacy Statement.

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