Study Coordinator, LPN

2 weeks ago

Rochester, United States Dermatology Associates of Rochester Full time
Job DescriptionJob DescriptionDescription:

About Skin Search: Skin Search is at the forefront of dermatological research. Our facility conducts Phase I, II, III, and IV FDA-approved clinical trials, focusing on medical dermatology, cosmetic dermatology, and device trials. By joining our clinical trials, volunteers contribute to the advancement of new medications and therapies, while enjoying a unique medical experience.

At Skin Search, we are committed to delivering extraordinary medical expertise and patient engagement, similar to what is experienced by our medical and cosmetic dermatology patients. Our research volunteers benefit from participation without incurring out-of-pocket costs, receive compensation for travel, and are not required to provide health insurance information.


Job Summary: Skin Search is seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team in Rochester, NY. The Clinical Research Coordinator will be responsible for managing and coordinating clinical trials, ensuring compliance with regulatory requirements, and providing exceptional care and support to our research volunteers. The position is full time, 32 hours per week.

Benefits:

  • Competitive pay and benefits package.
  • Opportunity to work with leading dermatologists and contribute to cutting-edge research.
  • Professional development and continuing education opportunities.
  • Supportive and collaborative work environment.
Requirements:

Key Responsibilities:

  • Coordinate and manage clinical trials from initiation to completion, ensuring adherence to study protocols and regulatory guidelines.
  • Recruit, screen, and enroll research volunteers, providing them with detailed information about the study and obtaining informed consent.
  • Schedule and conduct study visits, collecting and recording data accurately.
  • Monitor study participants for safety and adverse events, ensuring their well-being throughout the trial.
  • Collaborate with investigators, sponsors, and regulatory authorities to ensure smooth conduct of trials.
  • Maintain accurate and up-to-date study documentation, including case report forms, source documents, and regulatory binders.
  • Ensure compliance with Good Clinical Practice (GCP) and FDA regulations.
  • Coordinate with Dermatology Associates of Rochester to leverage medical expertise and resources.
  • Provide exceptional patient engagement and support, addressing any questions or concerns from research volunteers.

Qualifications:

  • NYS Nursing License (LPN, RN)
  • Previous experience in clinical research, preferably in dermatology, is highly desirable.
  • Knowledge of FDA regulations and GCP guidelines.
  • Excellent organizational and time management skills, with the ability to manage multiple tasks simultaneously.
  • Strong interpersonal and communication skills, with the ability to engage and support research volunteers.
  • Detail-oriented with a high degree of accuracy in data collection and documentation.
  • Proficiency in using electronic data capture systems and Microsoft Office Suite.
  • Ability to work independently and as part of a team in a fast-paced environment.

Join Skin Search and be a part of our mission to advance dermatological research and improve patient outcomes through innovative clinical trials.

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