Clinical Research Coordinator Jobs

Title: Clinical Research Coordinator
Duration: 2 Years
Location: Charlotte, NC
Job Summary
The Clinical Research Coordinator will be an essential team member in active clinical research, overseeing an ongoing Phase III clinical trial. The Research Coordinator oversees day-to-day progress of the clinical trial, and performs various patient-facing and regulatory tasks. To be successful in this role, the candidate should possess strong organizational skills, outstanding interpersonal skills, and a desire to contribute to clinical research and development. General responsibilities include consenting subjects, recruiting patients, performing study visits, assisting investigators with procedures, collecting, entering, and managing data, and maintaining regulatory documentation and submissions.
Essential Responsibilities
Performs subject-related tasks, such as screening and consenting, conducting chart review and prescreening, collecting samples, and assisting with procedures.
Maintains clear, concise, and organized records in line with GCP.
Acts as the primary point of contact for study participants.
Conducts data management activities, including collection and entry, and assessment for accuracy.
Assists with preparation and maintenance of all regulatory documentation.
Builds and maintains strong relationships with research subjects, teams, collaborators, and colleagues.
Adheres to all protocol, policy, and regulatory requirements required to conduct human subject's research.
Asks questions and solves problems proactively.
Skills And Abilities
Excellent interpersonal skills to interact with investigators, study staff, CRO/Sponsor, and research subjects.
Sound organizational skills with the ability to manage multiple priorities effectively.
Ability to maintain confidentiality.
Responsible and punctual individual.
Knowledge of protocol adherence and advanced research practices.
Ability to be on-site for all patient visits and to perform regulatory maintenance.
Education
Bachelor's Degree (Required)
Experience
One year of related experience, required. 2-3 years of related experience, preferred. Prior experience with urological clinical trials, preferred.