Back to the roster

Clinical Research Specialist I (Clinical Trials) - Remote

Remote Full-time Hiring now

We are seeking a Clinical Research Specialist I to join our team in a 100% remote capacity. This role requires experience as a Research Specialist in clinical trials. The position is fully remote; however, candidates must reside in an approved state. Work hours are Monday through Friday, either 900 AM - 530 PM or 800 AM - 430 PM. The Clinical Research Specialist I provides clinical research expertise by participating in the design and implementation of research projects as needed. Responsible for specific and assigned aspects of research infrastructure development, coordinates projects, and communicates status and improvement areas to leadership. May implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Duties and Responsibilities

  • Provides clinical research expertise by participating in the design and implementation of research projects as needed by the department or institution.
  • Responsible for specific and assigned aspects of research infrastructure development and/or maintenance.
  • Coordinates research projects at an institutional or departmental level.
  • Communicates project status and improvement areas with leadership in a timely manner.
  • Projects may include, but are not limited to investigator-initiated protocol development including protocol writing, case report form development, budget development, and coordination of departmental research committees.
  • May implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts.
  • Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
  • Maintains research practices using Good Clinical Practice (GCP) guidelines.
  • Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
  • Participates in required training and education programs. Apply tot his job Apply To this Job

Apply To This Job

Related roles

Clinical Research Associate II - Neuro & Immunology (Remote US - Multiple Openings)

Remote Full-time

Senior Clinical Research Associate - Oncology - East Coast - Remote

Remote Full-time

Clinical Research Associate II - Neuro & Immunology (Remote US - Multiple Openings)

Remote Full-time

[Remote] Senior Data Scientist, Clinical Research

Remote Full-time

Principal Clinical Research Associate- Shockwave (Reducer)

Remote Full-time

Senior Clinical Research Associate - Freelance

Remote Full-time

Staff Pharmacist, Hiring ASAP- Remote

Remote Full-time

Telehealth Nurse (4-Day Work Week on site)

Remote Full-time

Occupational Telehealth Nurse (LVN or RN – Night Shift)

Remote Full-time

Telephonic Case Manager

Remote Full-time

Part-Time Remote Data Entry Specialist – Flexible Home-Based Position | Accuracy-Focused Data Management Role at arenaflex

Remote Full-time

Global LMS Help and Support Lead (Remote)

Remote Full-time

Freelance Illustrator – Character Art & Pattern Design

Remote Full-time

Scrum Master/Team Coach III

Remote Full-time

Experienced Call Center Representative – Remote Data Entry Work at arenaflex

Remote Full-time

Experienced Customer Support Specialist II – Unlocking Opportunities for Consumers and Businesses

Remote Full-time

Sr. Power Electronics Engineer

Remote Full-time

Experienced Remote Data Entry Clerk – Entry-Level Opportunity with Comprehensive Training and Career Advancement

Remote Full-time

Experienced Remote Chat Support Agent – Public Relations and Crisis Management

Remote Full-time

Experienced Full Stack Social Media Customer Support Representative – Remote Workforce Management

Remote Full-time