On-Site Clinical Research Coordinator — Trials & Data

Invitek Molecular GmbH

Irving (TX)

On-site

USD 26,000 - 32,000

Full time

5 days ago

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Job summary

ALS is seeking a Clinical Research Coordinator to plan, coordinate, and execute clinical studies at our Irving, TX site. You will support safety and efficacy studies under the supervision of the Principal Investigator and manage study data, consent forms, and study materials.

This role requires a bachelor’s degree in life sciences, familiarity with Good Clinical Practice, and 1–2 years of clinical experience.

Qualifications

Bachelor’s degree from a 4 year university.
Life sciences degree preferred.
Current certificate for Human Protections, Good Clinical Practices, Bloodborne Pathogens.
1–2 years’ experience in clinical industry experience.

Responsibilities

Coordinate and support planning, initiation, implementation, and day-to-day execution of clinical research studies.
Prepare, organize, and maintain study materials and documentation (consent forms, screening, medical history, source documents).
Explain study procedures to participants and obtain informed consent.
Prepare study areas, patches, supplies, and related materials for study conduct.
Receive, log, weigh, prepare, fill, and dispose of test articles per protocol and safety rules.
Monitor subject responses, record adverse events, and maintain study records with accuracy.