Clinical Trials Documentation Specialist

PSG Global Solutions; Illinois City (IL); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading clinical research organization in Illinois is seeking candidates to join their clinical team. The role involves conducting Phase I-IV studies, ensuring compliance with regulations, and supporting document management. The ideal candidate will have a Bachelor’s degree and experience in the pharmaceutical field, alongside strong documentation and organizational skills. The position offers opportunities for career development in a collaborative environment.

Qualifications

• Bachelor’s degree required.
• Pharma experience or professional equivalent is required.
• Ideal candidates will possess strong organizational capabilities.

Responsibilities

• Conduct Phase I-IV studies according to Federal Regulations and ICH guidelines.
• Support clinical team with organizing and filing study documents.
• Assist Clinical Team members with data queries and record reconciliation.

Skills

Strong documentation or research experience

Ability to prioritize multiple tasks

Strong organizational capabilities

Strong interpersonal skills

Excellent written and verbal skills

Education

Bachelor’s degree

Job description

A leading clinical research organization in Illinois is seeking candidates to join their clinical team. The role involves conducting Phase I-IV studies, ensuring compliance with regulations, and supporting document management. The ideal candidate will have a Bachelor’s degree and experience in the pharmaceutical field, alongside strong documentation and organizational skills. The position offers opportunities for career development in a collaborative environment.