Clinical Research Specialist - GCP & Site Ops

Advanced Clinical; Coon Rapids (MN); In loco; USD 65.000 - 90.000; Tempo pieno

Vantaggi offerti da questo lavoro

Health coverage

Life insurance

Disability insurance

401k benefits

Descrizione del lavoro

Advanced Group is seeking a Clinical Research Specialist to support the execution and oversight of clinical studies in Minnesota. You will assist with site management, study documentation, clinical systems, and operational activities to ensure studies comply with GCP and regulatory requirements.

Responsibilities include coordinating site management and communications, maintaining trial records, and reviewing data and metrics to drive compliant deliverables.

Competenze

• Bachelor's degree in Life Sciences, Healthcare, Nursing, or a related field.
• 1–2+ years of experience in clinical research, clinical operations, or site management.
• Experience with CTMS, EDC, TMF, or similar clinical systems.
• Knowledge of GCP guidelines and clinical trial regulations.

Mansioni

• Support clinical studies from startup through closeout.
• Coordinate site management, study documentation, and stakeholder communications.
• Maintain clinical systems, study records, and trial documentation.
• Review study data, metrics, and operational deliverables.
• Support site, vendor, and investigator interactions.
• Identify and escalation study risks, issues, and compliance concerns.
• Ensure compliance with GCP, SOPs, and regulatory requirements.

Conoscenze

Organizational skills

Communication skills

Cross-functional teamwork

Problem-solving

CTMS/EDC/TMF

Formazione

Bachelor's degree in Life Sciences or related field

Strumenti

CTMS

EDC

TMF

Descrizione del lavoro

Advanced Group is seeking a Clinical Research Specialist to support the execution and oversight of clinical studies in Minnesota. You will assist with site management, study documentation, clinical systems, and operational activities to ensure studies comply with GCP and regulatory requirements.

Responsibilities include coordinating site management and communications, maintaining trial records, and reviewing data and metrics to drive compliant deliverables.