Clinical Research Coordinator

Overview

Coordinate dermatology clinical trials, managing patients, data, and regulatory compliance.

Key Responsibilities

• data management
• drug accountability
• crf management
• patient visits
• recruitment
• regulatory compliance

Tasks

-Administer questionnaires, diaries, and other participant materials as per protocol. -Maintain accurate case report forms and cross-reference patient medical records for completeness and FDA compliance. -Manage investigational medications, including receiving, dispensing, and performing drug accountability. -Ensure necessary supplies and equipment are available and functional for each study. -Collect, enter, and manage clinical data while maintaining confidentiality. -Manage and oversee the execution of clinical trials under the direction of the Principal Investigator and Site Manager. -Conduct patient visits and ensure adherence to study protocols, including collecting and processing biological specimens and performing procedures such as ECGs and vital signs monitoring. -Actively participate in recruiting and screening study participants. -Collaborate with laboratories to process, ship, and ensure review of investigational reports. -Schedule and coordinate research visits, assessments, and procedures, ensuring all requirements are met. -Monitor study participants to ensure adherence to study guidelines and ethical standards. -Comply with company policies, HIPAA, OSHA regulations, and Standard Operating Procedures to deliver high-quality services. -Maintain organized records of study materials, ensuring all regulatory documentation is up to date.

Requirements

• bachelor's
• phlebotomy
• gcp
• clinical trials
• bilingual
• problem solving

What You Bring

-Bachelor’s or Master’s degree in a related field is preferred. -Phlebotomy certification is preferred. -with proficiency in Good Clinical Practices (GCP) and FDA regulations. -High School Diploma or GED is required. -Previous experience conducting clinical trials, including recruitment and compliance with regulatory guidelines. -Bilingual in Spanish or Vietnamese is preferred. -Ability to take direct feedback and possess strong problem-solving skills. -Certification as a Clinical Research Coordinator (CCRC) is preferred. -Excellent bedside manner and soft skills.

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Benefits

-Medical, dental & vision -Health Spending Account (HSA) -Short and long-term disability -Critical Illness, Accident, and Hospital -401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available -Employee Assistance Program -Life Insurance (Voluntary Life & AD&D for the employee and dependents) -Transportation benefits -Time Off/Leave (PTO, Vacation or Sick Leave)

About Actalent

-Born in July 2021 by merging Aerotek’s engineering & sciences arm with EASi, Actalent emerged as a focused engineering-and-science partner. -Backed by Allegis Group, it drives scale and speed to market via contract, managed, and technical services. -Headquartered in Maryland with global reach, it deploys specialized teams across North America, Europe, and APAC on Fortune 500 projects. -Typical engagements span EV design, vaccine development, lab services, clinical research, and infrastructure systems. -Expertise covers a wide spectrum: aerospace, defense, healthcare, manufacturing, software systems, environmental and civil engineering.

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