In-house CRA I

9 hours, 28 minutes ago
Full-time
Entry Level
Operations
Precision Medicine Group

Precision Medicine Group

Precision Medicine Group specializes in precision medicine, utilizing targeted expertise and data insights to accelerate drug development and enhance the commercialization of next-generation medical products for the pharmaceutical and life sciences ind...

Pharmaceuticals
251-1K
Founded 2012

Description

  • Support study sites and clinical project teams throughout clinical research studies.
  • Serve as a point of contact and liaison for study sites and site management issues.
  • Assist with investigator recruitment, site feasibility, and site selection activities.
  • Prepare and distribute Investigator Site Files and coordinate with shipping vendors when needed.
  • Collect, review, organize, and maintain essential documents and site-level TMF records.
  • Update site-related data in clinical systems, including CTMS and study trackers.
  • Track milestones, activities, data entry, and study reporting to ensure accuracy and completeness.
  • Support study supplies, sample logistics, and investigational product accountability when applicable.
  • Assist with local regulatory, IRB/IEC, and sponsor submission requirements.
  • Review site data, query resolutions, and support database freeze and closeout activities.
  • Follow up on trial invoices and help ensure timely processing of investigator payments.
  • Document site and sponsor interactions professionally and in a timely manner.

Requirements

  • Bachelor's degree or international equivalent, or an equivalent combination of education and experience, ideally in a business, scientific, or healthcare discipline.
  • Proven ability to learn the skills required for the In-house CRA role.
  • Advanced knowledge of Microsoft Office applications, including Outlook, Word, Excel, and PowerPoint.
  • Ability to communicate verbally and in writing in English.
  • Customer service-oriented demeanor with flexibility and teamwork.
  • High attention to detail and accuracy for extended periods of time.
  • Transferable experience from a related healthcare field.
  • Ability to travel as needed.
  • Good organizational skills (preferred).
  • Ability to work efficiently in a remote work environment (preferred).
  • Working knowledge of ICH-GCP, Precision SOPs, and regulatory guidance (preferred competency).
  • Strong interpersonal, written, verbal, and presentation skills (preferred competency).

Benefits

  • Remote work environment (#LI-Remote).
  • Opportunity to work in a role supporting multiple clinical studies across regions.
  • Equal Opportunity Employer status and non-discriminatory hiring practices.
  • Reasonable accommodation support for candidates with disabilities during the application process.

Interested in this position?

Apply directly on the company website

Apply Now

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