Clinical Research Coordinator (FWSCC)

DermCare Management; Orlando (FL); On-site; USD 65,000 - 75,000; Full time

Job summary

A leading healthcare management company is seeking a Clinical Research Coordinator to oversee clinical trials. The role requires excellent interpersonal skills and adherence to regulatory standards. Responsibilities include managing trials, engaging with participants, and ensuring compliance with guidelines. Ideal candidates will have a medical background and strong organizational skills.

Qualifications

• Exceptional interpersonal skills required.
• Willingness to continually self-educate.

Responsibilities

• Oversee the smooth running of clinical trials.
• Monitor research participants to ensure adherence to study rules.
• Engage with subjects and manage visit flow.

Skills

Attention to detail

Interpersonal skills

Communication

Organizational skills

Self-education

Education

CCRC certification

Job description

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We 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 perform required visit procedures, administer questionnaires and subject materials, adhere to regulatory trial standards, and participate in subject recruitment efforts, among other duties.

Clinical research coordinators need to engage with research investigators, pharmaceutical companies (sponsors), contract research organizations (CROs), and research subjects, requiring excellent interpersonal and communication skills.

Clinical Research Coordinator Responsibilities

• Oversee the smooth running of clinical trials.
• Perform clinic visits as per the protocol, GCP, and FDA guidelines.
• Complete procedures such as phlebotomy, EKGs, Vitals, assessments.
• Collect and enter data obtained for the trial.
• Inform participants about study objectives.
• Administer questionnaires.
• Monitor research participants to ensure adherence to study rules.
• Adhere to research regulatory standards and ethical standards.
• Maintain detailed records of studies as per FDA guidelines and regulatory documentation.
• Manage investigational medication, including receiving, dispensing, storing, and performing accountability.
• Liaise with laboratories, process, ship, and ensure investigators review reports.
• Participate in subject recruitment efforts.
• Ensure necessary supplies and equipment for the study are in stock and in working order.
• Engage with subjects, understand their concerns, and manage visit flow as indicated in the protocol.

Qualifications

• Attention to detail.
• Exceptional interpersonal skills.
• Good computer and technical skills.
• Outstanding written and verbal communication.
• Excellent organizational skills.
• Willingness to continually self-educate.
• CCRC certification is a plus.
• Bi-lingual in Spanish is a plus.

Seniority level

• Entry level

Employment type

• Other

Job function

• Research, Analyst, and Information Technology

Industries

• Hospitals and Health Care

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Riverview, FL $65,000.00-$75,000.00 3 weeks ago