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Clinical Research Project Coordinator

2 months ago

Texas, United States SQRL Full time

Exciting opportunity to become a key player in a thriving Clinical Research Site Network.

Key Highlights

  • Salary Range: $55,000 - $65,000 based on experience
  • Engage in impactful clinical trials that contribute to healthcare advancements
  • Comprehensive Benefits Package (Health, Dental, Vision, 401k with 4% Match, Paid Time Off, Paid Holidays)
  • Acquire valuable experience in the rapidly evolving field of clinical research and enhance your in-demand skills
  • Standard Work Hours: Monday to Friday, 8 AM to 5 PM

Role Overview

The Clinical Trial Coordinator will oversee a range of intricate activities and execute tasks related to the initiation, execution, and conclusion of clinical pharmaceutical and device research protocols. Responsibilities include ensuring the collection of clean, objective, and precise data within sponsor timelines while adhering to relevant Standard Operating Procedures (SOPs), policies, federal regulations, medical ethics, Good Clinical Practices (GCPs), International Council of Harmonization (ICH) guidelines, Institutional Review Board (IRB) standards, and specific sponsor protocol requirements. All duties must align with the company's Core Values, Mission Statement, and Employee Manual.

About the Company

SQRL is a network of Clinical Research sites operating across multiple states, specializing in conducting Phase I-IV trials in various therapeutic areas, including cardiology, metabolic disorders, renal conditions, central nervous system (CNS) studies, pulmonology, and vaccine research.

Qualifications

  • Experience in Phlebotomy, EKGs, and Vital Signs is highly desirable
  • A minimum of 1+ years' experience as a Clinical Research Coordinator is required.
  • Education: A Bachelor's degree is preferred but not mandatory.
  • In-depth knowledge of clinical research methodologies.
  • Strong leadership and management capabilities with the ability to think independently and influence stakeholders as needed. Proficient in negotiation and conflict resolution.
  • Proven ability to collaborate effectively and align with operational goals.
  • Excellent verbal and written communication skills, along with proficiency in Office 365 applications. Experience in drafting and reviewing Standard Operating Procedures is a plus.
  • Strong analytical skills in problem-solving, risk assessment, and impact analysis. Demonstrated experience in process improvement. Must be adaptable and capable of managing multiple priorities.