Onsite Clinical Research Coordinator - Contract to Perm

System One, Inc.; West Chester (Chester County); Sur place; USD 36 000 - 41 000; Plein temps

Résumé du poste

System One, Inc. is seeking a Clinical Research Coordinator to support the coordination and execution of clinical research protocols onsite in West Chester, Pennsylvania.

The role entails handling screening, consent, enrollment, scheduling, data capture, and regulatory compliance under supervision. Ideal candidates have medical terminology experience, strong organizational skills, and familiarity with GCP/HIPAA.

Qualifications

• High school diploma or equivalent; associate degree or higher in health-related field preferred.
• Basic knowledge of clinical research preferred.
• Medical terminology & patient care experience required.
• Strong organizational, time-management and attention-to-detail skills.
• Ability to communicate clearly and professionally with diverse populations.
• Ability to work collaboratively in a fast-paced, team-oriented environment.
• Knowledge of GCP, HIPAA, ALCOA, FDA regulations, and IATA guidelines strongly preferred.
• Experience with participant screening and informed consent processes preferred.
• Proficiency with electronic data capture systems and clinical trial management software; MS Office preferred.
• Medical Assistant (MA) certification preferred.
• Current CPR/BLS certification preferred.
• Certification as a Clinical Research Coordinator (e.g., CCRC) or willingness to obtain certification preferred.

Responsabilités

• Assist in coordination and execution of clinical research protocols under supervision.
• Conduct screening visits to collect medical history and other info from participants.
• Assist with informed consent and enrollment per protocol and ethics.
• Schedule study visits, procedures, and follow-up with participants and teams.
• Collect, record and maintain accurate data and source documentation.
• Communicate with participants to educate and support adherence.
• Monitor progress and report adverse events and deviations to the team.
• Adhere to SOPs and GCP guidelines.
• Draw, process, and ship lab specimens where qualified.
• Scan and file study records; maintain organized documentation.
• Apply critical thinking to support operations and problem resolution.
• Perform other duties as assigned.

Connaissances

Medical terminology & patient care

Organizational & time management

Clear communication

Team collaboration

GCP/HIPAA/ALCOA/FDA/IATA knowledge

Electronic data capture familiarity

MS Office proficiency

Formation

High school diploma or equivalent; associate degree or higher in health-related field preferred

Outils

Electronic data capture systems

Clinical trial management software

Microsoft Office (Excel/Word/PowerPoint)

Description du poste

System One, Inc. is seeking a Clinical Research Coordinator to support the coordination and execution of clinical research protocols onsite in West Chester, Pennsylvania.

The role entails handling screening, consent, enrollment, scheduling, data capture, and regulatory compliance under supervision. Ideal candidates have medical terminology experience, strong organizational skills, and familiarity with GCP/HIPAA.