Clinical Research Coordinator

Position Overview

Clinical Research Coordinator responsible for planning, coordinating, and executing clinical research studies, including collection and management of trial data.

• Plan, coordinate, and execute clinical research studies, including collection and management of clinical trial data.
• Support safety and efficacy studies under the supervision of the Principal Investigator, in accordance with approved study protocols, company standard operating procedures, and Good Clinical Practice guidelines.
• Perform all assigned responsibilities necessary to support compliant, accurate, and efficient study execution.

To be eligible to work at ALS, you must be a citizen or permanent resident of the country you are applying for, or hold or be able to obtain a valid working visa.

ALS is proud to be an equal opportunity employer and is committed to fostering an inclusive work environment where the strengths and perspectives of each employee are both recognised and valued. Qualified candidates will be considered without regard to race, colour, religion, national origin, military or veteran status, gender, age, disabilities, sexual orientation, gender identity, pregnancy and pregnancy‑related conditions, genetic information and any other characteristics protected by the law.

We invite resumes from all interested parties, including women, members of minority groups, and persons living with disabilities. ALS also welcomes applications from people with all levels of ability. Reasonable adjustments to support candidates throughout the recruitment process are available upon request.