Job detail

Clinical Research Coordinator

Rovia Clinical Research

#Vital Signs #Regulatory Compliance #Phlebotomy #Patient Experience #Patient Safety #SOPs #Clinical Research #EKG #Clinical Trials

Quick overview

The coordinator is responsible for executing clinical trials by managing patient visits, performing clinical tasks, and ensuring protocol adherence. They also handle data entry, source documentation, and maintain investigational product accountability.

Requirements summary

A high school diploma is required, though a bachelor's degree in a related field is preferred. Candidates should have at least one year of clinical research experience and proficiency in patient-facing clinical activities.

high schoolbachelor degreeMultitaskingOrganizational SkillsPhlebotomyMedical TerminologyMicrosoft OfficePatient CommunicationVital SignsPatient ConfidentialityData IntegritySpecimen CollectionEKGClinical ProceduresRegulatory RequirementsEDCCTMSICH/GCP

Job description

Position Summary

The Clinical Research Coordinator (CRC) is responsible for coordinating and executing clinical trials in accordance with study protocols, ICH/GCP guidelines, sponsor requirements, and Rovia SOPs. This role partners closely with site teams to support study startup, enrollment, data quality, and overall study success.

Key Responsibilities

Conducts and coordinates patient visits in accordance with study protocols.
Performs clinical tasks such as vital signs, EKGs, specimen collection and processing, and phlebotomy as applicable.
Ensures informed consent is properly obtained and documented.
Educates and guides participants through the study, ensuring a positive patient experience.
Monitors subject safety, reports adverse events, and escalates concerns as appropriate.
Completes timely and accurate source documentation and EDC data entry.
Resolves data queries and ensures data integrity.
Maintains investigational product accountability and proper storage and handling.
Prepares for and supports monitoring visits, audits, and inspections.
Collaborates with site staff and investigators to ensure protocol adherence and efficient visit flow.
Perform other duties as assigned.

Skills/Abilities

Strong knowledge of medical terminology and clinical procedures.
Understanding of ICH/GCP and regulatory requirements.
Excellent organizational skills and attention to detail.
Strong interpersonal and patient-facing communication skills.
Ability to multitask and manage competing priorities in a fast-paced environment.
Proficiency in Microsoft Office, EDC, and CTMS applications.
Ability to work both independently and collaboratively.
High level of professionalism and commitment to patient confidentiality.

Education/Experience

High school diploma required, bachelor’s degree in related field preferred.