Clinical Research Lead: Protocols, IRB & Site Coordination

JAX; Farmington (CT); Sur place; USD 70 000 - 101 000; Plein temps

Résumé du poste

The Jackson Laboratory seeks a Clinical Research Specialist to support investigators and clinical collaborators by contributing site and regulatory expertise to grants and protocol design. You will help ensure studies meet GCP, policies, and procedures.

Responsibilities include IRB coordination, site management, protocol development, and training on compliance for investigators and staff. A Master’s in health sciences plus 3+ years of clinical research experience are required.

Qualifications

• Three+ years of patient-facing clinical research experience in academia or clinical settings.
• Knowledge of clinical study design, regulatory requirements, and IRB processes.
• Strong written and oral communication for cross-disciplinary collaboration.

Responsabilités

• Support development of clinical study proposals and protocols for funded grants.
• Manage clinical site identification, startup, and IRB submission support.
• Develop SOPs and training materials for clinical research compliance.

Connaissances

Study design

Statistical analysis

Protocol development

Informed consent

IRB regulations

Communication skills

Collaboration

Prioritization

Organization

Customer service

Formation

Master’s degree in health sciences or related field

Description du poste

The Jackson Laboratory seeks a Clinical Research Specialist to support investigators and clinical collaborators by contributing site and regulatory expertise to grants and protocol design. You will help ensure studies meet GCP, policies, and procedures.

Responsibilities include IRB coordination, site management, protocol development, and training on compliance for investigators and staff. A Master’s in health sciences plus 3+ years of clinical research experience are required.