Job detail

Clinical Research Coordinator (FWSCC)

DERMCARE MANAGEMENT LLC

#Interpersonal Skills #Record Keeping #Phlebotomy #EKGs #FDA Regulations #Regulatory Standards #Monitoring #Clinical Research #Data Collection #Ethical Standards #Clinical Trials #Good Clinical Practice

Other On Site 0-2 yrsPosted 5 months ago

Location

Tampa, Florida

Quick overview

Clinical research coordinators oversee the smooth running of clinical trials and perform clinic visits according to protocols and regulations. They are responsible for collecting data, informing participants about study objectives, and ensuring adherence to study rules.

Requirements summary

Candidates should possess exceptional interpersonal skills and attention to detail, along with good computer and technical skills. A CCRC certification and bilingual ability in Spanish are considered a plus.

Attention To DetailInterpersonal SkillsWritten CommunicationVerbal CommunicationOrganizational SkillsBilingualComputer SkillsTechnical SkillsSelf-EducationCCRC Certification

Job description

Job DetailsJob Location

Florida West Coast Skin and Cancer Center (FWSCC) - Tampa, FL 33607We are looking for candidates with medical backgrounds and excellent interpersonal skills for the position of clinical research coordinator. Clinical research coordinators are responsible for conducting clinical research trials by adhering to Good Clinical Practice (GCP), International Air Transportation (IATA) and FDA regulations. The candidate will be performing required visit procedures, administering questionnaires and subject material, adhering to regulatory trial standards, and participating in subject recruitment efforts, among other duties. Clinical research coordinators need to engage with the research investigators, pharmaceutical companies (sponsors) and contract research organizations (CROs) as well as the research subjects requiring excellent interpersonal and communicative skills.

Responsibilities: Overseeing the smooth running of clinical trials. Performing clinic visits as per the protocol, GCP and FDA Completing procedures such as phlebotomy, EKGs Vitals, assessments Collecting and entering data obtained for the trial Informing participants about study objectives. Administering questionnaires. Monitoring research participants to ensure adherence to study rules. Adhering to research regulatory standards. Adhering to ethical standards. Maintaining detailed records of studies as per FDA guideline and regulatory documentation Managing investigational medication including receiving, dispensing, storing and performing accountability Liaising with laboratories process, ship and ensure investigators review reports Participating in subject recruitment efforts. Ensuring that the necessary supplies and equipment for a study are in stock and in working order. Engaging with subjects and understanding their concerns and managing the visit flow as indicating in the protocol.