Collaborative Clinical Trial Operations Coordinator

Pinnacle Clinical Research- A Summit Solution

Corpus Christi (TX)

On-site

USD 60,000 - 75,000

Full time

46 hours ago
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Job summary

Pinnacle Clinical Research- A Summit Solution is seeking a Clinical Research Coordinator to manage day-to-day trial operations, recruit participants, document activities, and ensure regulatory compliance. Strong communication and organization are essential as you collaborate with sponsors and vendors to meet study goals.

The ideal candidate will multitask effectively, maintain confidentiality, and communicate in English and Spanish.

Qualifications

  • 1 year of experience as a Clinical Research Assistant or Coordinator.
  • Bachelor’s Degree in a scientific area of study preferred or equivalent combination of education, training, and experience.
  • Must have strong knowledge of ICH/GCP guidelines.
  • Must complete GCP training before interacting with participants and recertify every 2 years or as applicable.
  • Trained and certified in Fibroscan and memory screens as required by the study portfolio.
  • Must have basic life support (BLS) training, provided during onboarding.
  • Proficient in Spanish and English preferred.

Responsibilities

  • Recruit and screen study participants per protocol.
  • Document and report daily trial activities.
  • Maintain participant privacy and data confidentiality.
  • Coordinate study-related visits and assessments.
  • Collaborate with sponsors and vendors.
  • Track enrollment and status reports.
  • Prepare memos, emails, and study reports.
  • Ensure regulatory documents are current.

Skills

Excellent communication
Organization & multitasking
Team collaboration
Attention to detail
Bilingual English/Spanish

Education

Bachelor’s Degree in a scientific field
High school diploma or GED

Tools

Microsoft Office
CRIO/CTMS

Job description

Pinnacle Clinical Research- A Summit Solution is seeking a Clinical Research Coordinator to manage day-to-day trial operations, recruit participants, document activities, and ensure regulatory compliance. Strong communication and organization are essential as you collaborate with sponsors and vendors to meet study goals.

The ideal candidate will multitask effectively, maintain confidentiality, and communicate in English and Spanish.

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