Clinical Research Specialist: Protocol Design & Site Oversight

The Jackson Laboratory

Farmington (CT)

Sur place

USD 70 000 - 101 000

Plein temps

Il y a 6 jours
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Résumé du poste

The Jackson Laboratory seeks a Clinical Research Specialist to support investigators and clinical collaborators in designing and implementing clinical studies in compliance with GCP and regulations. The role involves proposal development, site identification, IRB submissions, and SOP maintenance, under the DCTRS.

Ideal candidates hold a master’s in health sciences or related fields and have at least three years of patient-facing clinical research experience within academic or clinical settings.

Qualifications

  • Master’s degree in health sciences or a relevant scientific area (e.g. epidemiology, clinical research administration, public health, biology).
  • Experience in patient-facing clinical research (study coordination) in an academic or clinical setting.
  • Knowledge of clinical study design, IRB regulations and informed consent processes.

Responsabilités

  • Support development of clinical study protocols, grant proposals and IRB submissions.
  • Identify and qualify clinical sites; prepare initial IRB submission materials and recruitment plans.
  • Contribute to SOPs and educational programs on compliance with regulations and policies.
  • Collaborate with investigators and staff to move projects forward through IRB processes.

Connaissances

Excellent written and oral comms
Strong organizational skills
Interpersonal skills
Multitasking and prioritization

Formation

Master’s Degree in health sciences or relevant field

Description du poste

The Jackson Laboratory seeks a Clinical Research Specialist to support investigators and clinical collaborators in designing and implementing clinical studies in compliance with GCP and regulations. The role involves proposal development, site identification, IRB submissions, and SOP maintenance, under the DCTRS.

Ideal candidates hold a master’s in health sciences or related fields and have at least three years of patient-facing clinical research experience within academic or clinical settings.

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