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Skills
Adverse Eventsunmatched
Certified Medical Assistantunmatched
Clinical Assessmentunmatched
Clinical Researchunmatched
Clinical Trial Managementunmatched
Communication Skillsunmatched
Data Entryunmatched
Data Qualityunmatched
Detail Orientedunmatched
Documentationunmatched
Electrocardiogramunmatched
Electronic Data Capture (EDC)unmatched
GCP (Good Clinical Practices)unmatched
High School Diplomaunmatched
ICH Regulationsunmatched
Informed Consentunmatched
Interpersonal Skillsunmatched
Investigational New Drug (IND)unmatched
Maintain Complianceunmatched
Medical Assistanceunmatched
Medical Terminologyunmatched
Medical Treatmentunmatched
Microsoft Officeunmatched
Multitaskingunmatched
Organizational Skillsunmatched
Patient Confidentialityunmatched
Phlebotomyunmatched
Regulatory Requirementsunmatched
Research Protocolsunmatched
Sample/Specimen Processingunmatched
Specimen Collectionunmatched
Standard Operating Procedures (SOP)unmatched
Startupunmatched
Time Managementunmatched
Description
Position Summary:
The Clinical Research Medical Assistant 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:
Conduct and coordinate patient visits in accordance with study protocols.
Perform clinical tasks such as vital signs, ECGs, specimen collection/processing, and phlebotomy (as applicable).
Ensure informed consent is properly obtained and documented.
Educate and guide participants throughout the study, ensuring a positive patient experience.
Monitor subject safety, report adverse events, and escalate concerns as appropriate.
Complete timely and accurate source documentation and EDC data entry.
Resolve data queries and ensure data integrity.
Maintain investigational product accountability and proper storage/handling.
Prepare for and support monitoring visits, audits, and inspections.
Collaborate 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.