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Clinical Research Coordinator

DermCare Management
USA
Full-time
Mid Level
Onsite
Discovered 1 months ago

Full Job Posting

  • 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, collecting and processing biological specimens (blood/urine) and performing procedures such as ECGs and vital signs monitoring.
  • Administer questionnaires, diaries, and other participant materials as per protocol.
  • Schedule and coordinate research visits, assessments, and procedures, ensuring all requirements are met.
  • Maintain accurate case report forms, cross-referencing patient medical records for completeness and FDA compliance.
  • Collect, enter, and manage clinical data while maintaining confidentiality.
  • Monitor study participants, ensuring adherence to study guidelines and ethical standards.
  • Manage investigational medications, including receiving, dispensing, and performing drug accountability.
  • Collaborate with laboratories to process, ship, and ensure review of investigational reports.
  • Actively participate in recruiting and screening study participants.
  • Maintain organized records of study materials, ensuring all regulatory documentation is up to date.
  • Ensure necessary supplies and equipment are available and functional for each study.
  • Complying with company policies, HIPAA, OSHA regulations, and Standard Operating Procedures (SOPs) to deliver high-quality services.
  • High School Diploma or GED
  • Preferred: Bachelor’s or master’s degree in a related field.
  • Required: Previous experience conducting clinical trials, including recruitment and compliance with regulatory guidelines.
  • Preferred: Certification as a Clinical Research Coordinator (CCRC).
  • Phlebotomy experience and certification where required.
  • Strong knowledge of medical terminology, clinical trial processes, and industry regulations.
  • Proficient with computer hardware and software, including clinical research databases.
  • Proficient in accessing, inputting, and retrieving data from a computer.
  • Strong attention to detail and organizational skills.
  • Ability to prioritize tasks, manage deadlines, and adapt to changing environments.
  • Ability to receive and process information through both oral and written communication.
  • Excellent problem-solving, leadership, and communication skills.
  • Outstanding interpersonal skills, with the ability to establish and maintain effective relationships with patients, investigators, and external partners.
  • Ability to work both independently and collaboratively as part of a team.
  • Ability to maintain confidentiality and handle sensitive information.
  • Willingness to learn and stay updated on new clinical research trends and regulations.
  • CCRC certification a plus.
  • Bi-lingual in Spanish is a plus.
  • Medical Insurance
  • Dental Insurance
  • Vision Insurance
  • Supplemental health benefits
  • Paid time off
  • Holidays
  • Retirement plan (401k)
  • Ability to sit or stand for 6-8 hours a day and lift or carry 5-10 pounds occasionally.
  • Requires substantial use of wrists, hands, and fingers for tasks such as typing and filing.
  • This position operates primarily in a professional office/clinical environment. The role regularly requires sitting, working at a computer, communicating with employees and managers.

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