ALS Global
Clinical Research Coordinator
Irving, Texas, United States of America
Work authorization requiredDetected 26 days ago
Clinical TrialsClinical ResearchResearchCollaborationGxP
About the role
- The Clinical Research Coordinator is responsible for the planning, coordination, and execution of clinical research studies, including the collection and management of clinical trial data.
- Position Duties and Scope: The essential duties and responsibilities of this position include, but are not limited to, the following.
- We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and our communities.
Responsibilities
- This role supports the conduct of safety and efficacy studies under the supervision of the Principal Investigator and in accordance with approved study protocols, company standard operating procedures, and current Good Clinical Practice guidelines.
- The incumbent performs all assigned responsibilities necessary to support compliant, accurate, and efficient study execution.
Requirements
- Bachelor's degree from a 4 year university
Nice to have
- Computer skills required
- 2 years' experience in clinical industry experience (substitute for BS or BA).
- Bachelor of Science or Arts degree in life sciences preferred.
Company info
- At ALS, we encourage you to dream big.
- When you join us, you'll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future.
Visa & Work Authorization
- To be eligible to work at ALS you must be a Citizen or Permanent Resident of the country you are applying for, or either hold or be able to obtain, a valid working visa.
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This listing is sourced directly from ALS Global's careers page and normalized into a canonical job model.