Clinical Research Coordinator (FWSCC)

Posted 5 Days Ago
Be an Early Applicant
2 Locations
In-Office or Remote
Entry level
Beauty • Healthtech • Professional Services
The Role
Coordinate and oversee clinical trial activities following GCP, IATA, and FDA regulations. Perform clinic visits, phlebotomy, EKGs, vitals, assessments, administer questionnaires, collect and enter trial data, manage investigational medication and supplies, maintain regulatory documentation, liaise with sponsors/CROs/labs, and support participant recruitment and study adherence.
Summary Generated by Built In

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 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.

 

Clinical Research Coordinator 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.
Qualifications

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 a plus
  • Bi-lingual in Spanish is a plus

Skills Required

  • Knowledge of Good Clinical Practice (GCP), IATA, and FDA regulations
  • Ability to perform phlebotomy, EKGs, vitals, and clinical assessments
  • Experience managing investigational medication (receiving, dispensing, storage, accountability)
  • Maintaining detailed regulatory and FDA-compliant study documentation
  • Exceptional interpersonal and communication skills (written and verbal)
  • Attention to detail and excellent organizational skills
  • Good computer and technical skills
  • Willingness to continually self-educate
  • CCRC certification
  • Bilingual in Spanish
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The Company
0 Employees

What We Do

DermCare Management is a dermatology practice management company that partners with dermatology and aesthetic medicine providers, offering operational and administrative support to help them focus on patient care and practice growth.

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