Clinical Research Coordinator

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.



Working at ALS
The ALS team is a diverse and dedicated community united by our passion to make a difference in the world.
Our values are important to us, and shape how we work, how we treat each other and how we recognise excellence.
At ALS, you’ll be supported to develop new skills and reach your full potential. We invest in our people with programs and opportunities that help you build a diverse career with us.
We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and our communities.

The Clinical Research Coordinator will be responsible for the execution of clinical trials and gathering clinical trial data by performing the duties outlined below. The training and duties for this job are adherent to all current good clinical practices.

• Disarms the building alarm.
• Prepares daily dilutions.
• Prepares patch booths, volatilized and non-volatilized patches and completes the Booth Check and Cart Logs.
• Creates and prints Sign in Sheets relevant to each day.
• Prints and organizes new study documents according to each study’s protocol (Examples include Informed Consent, Screener, Medical History Forms, check-off sheets, Urine Pregnancy Test Forms, studies calendar and/or diaries.)
• Prepares Study Administrative Notebook.
• Unlocks front door.
• Explains study procedures and consents subjects.
• Assigns and/or enters scores based upon the agreed upon scoring scale outlined in the study protocol.
• Records adverse events.
• Operates instruments during study execution and records data on appropriate study documents.
• Downloads pictures from camera into study folders.
• Updates Panelist Database.
• Performs initial jar fill, jar refill, and jar rinse.
• Logs in and weighs test articles.
• Prepares and updates data tables for studies.
• Creates final reports for QA and management review and submission to sponsors.
• Performs clerical duties:
• Greets Panelists.
• Uses copy and fax machines.
• Records panelist’s names and study numbers on the front desk list as they arrive for patch studies
• Performs weekly assigned duties:
• Archives folders.
• Cleans prep room.
• Assists Senior Clinical Research Coordinators and/or Clinical Research Supervisor with other tasks as assigned.
• Provides daily updates to PMs.
• Conducts product disposal, when needed and updates disposal log.

Performs duties to close business for the day which may include, but not limited to, the following:

• Locks front door.
• Disposes of dilutions.
• Disposes of used syringes and applicators.
• Restocks patch booths for next day (cotton balls, applicators, syringes, and blank patches).
• Prepares water and test article for the next scheduled daily dilution.
• Makes sure all instruments are turned off and instruments/probes are stored properly.
• Files paperwork in Study Administrative Notebook.
• Logs off all computers.
• Sets the building alarm.
• Turns off all lights.

Everyone Matters

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.
ALS also welcomes applications from people with all levels of ability. Reasonable adjustments to support candidates throughout the recruitment process are available upon request.

Eligibility

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.


How to apply
Please apply on-line and provide a cover letter and CV that best demonstrate your motivation and ability to meet the requirements of this role.