Clinical Research Coordinator

Als; Irving (TX); On-site; USD 37,000 - 50,000; Full time

Job summary

ALS is seeking a Clinical Research Coordinator to plan, coordinate, and execute clinical studies, including data collection and management.

Under supervision of the Principal Investigator, you will ensure compliance with GCP guidelines and SOPs and support study documentation and participant interactions.

This role requires a BS in life sciences and 1–2 years of clinical industry experience, with an hourly rate indicated.

Qualifications

• Bachelor’s degree from a 4 year university; life sciences preferred.
• Current certificates for Human Protections, Good Clinical Practices, Bloodborne Pathogens are preferred.

Responsibilities

• Coordinate and support planning, initiation, implementation, and day-to-day execution of clinical research studies in accordance with protocols and GCP guidelines.
• Prepare and maintain study materials and documentation (informed consent forms, screening materials, medical history forms, source documents, study logs).
• Explain procedures to participants and obtain informed consent; verify eligibility with the study team.
• Prepare areas and materials for study conduct, ensure proper preparation of equipment and supplies.
• Handle test articles and related materials per protocol and safety procedures.
• Monitor subjects and record adverse events; ensure accurate data entry in study records.
• Operate study instruments, collect data, and maintain study images/files.
• Maintain study data tables, logs, and tracking tools for oversight and reporting.

Education

Bachelor's degree in life sciences

Job description

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.

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.

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.

Hourly Rate: $21

Position Requirements/Essential Criteria:

Bachelor’s degree from a 4 year university Bachelor of Science or Arts degree in life sciences preferred. Certificates, licenses, and registrations preferred: Current certificate for: Human Protections, Good Clinical Practices, Bloodborne Pathogens Computer skills required 1 – 2 years’ experience in clinical industry experience (substitute for BS or BA).

Position Duties and Scope:

Specific responsibilities may vary based on assigned site, study type, protocol requirements, testing methodology, instrumentation, and operational needs.

• Coordinate and support the planning, initiation, implementation, and day‑to‑day execution of clinical research studies in accordance with study protocols, sponsor requirements, company standard operating procedures, and current Good Clinical Practice guidelines.
• Prepare, organize, and maintain study materials and documentation, including informed consent forms, screening materials, medical history forms, source documents, study calendars, diaries, sign‑in sheets, administrative notebooks, and other protocol‑required records.
• Explain study procedures to research participants, obtain informed consent, and help ensure that subject eligibility and entrance criteria are confirmed in collaboration with the Recruitment Department and study team prior to study participation.
• Prepare study areas, patch booths, test materials, volatilized and non‑volatilized patches, dilutions, and other supplies required for study conduct, and complete all applicable preparation, equipment, booth, cart, and study logs.
• Receive, log, weigh, prepare, fill, refill, rinse, and dispose of test articles and related materials in accordance with protocol requirements, safety procedures, and company guidelines.
• Conduct and coordinate daily clinical study activities to support efficient workflow, proper scheduling, and subject throughput while maintaining compliance with study requirements.
• Monitor research subjects’ responses during study participation, assign and/or enter protocol‑defined scoring, document observations, and accurately record adverse events and other study data in the appropriate study records.
• Operate study‑related instruments and equipment during study conduct, ensure proper data collection and documentation, download and maintain study images and electronic files, and verify that instruments are properly shut down and stored after use.
• Prepare, update, and maintain study data tables, panelist or subject databases, logs, and other tracking tools to support accurate study oversight and reporting.
• Collaborate with investigators, project managers, clinical management, and other internal departments to communicate study progress, provide status updates, and support the preparation of protocols, interim reports, final reports, and sponsor deliverables.
• Perform front‑desk, participant‑facing, and general administrative support activities, including greeting study participants, recording participant attendance, and handling routine clerical functions such as copying, faxing, printing, filing, and document organization.
• Maintain study files and administrative records in an inspection‑ready condition, including filing paperwork, archiving folders, and ensuring documentation is complete, current, and properly organized.
• Order, stock, restock, and maintain laboratory, clinic, and study supplies and materials necessary for ongoing research activities.
• Perform routine facility and study‑area opening and closing procedures, which may include unlocking and securing entrances, disarming and setting alarms, turning lights and equipment on or off, preparing materials for the next study day, and ensuring work areas are clean, stocked, and ready for use.
• Conduct cleaning, disposal, and housekeeping tasks related to study execution, including product disposal, dilution disposal, disposal of used supplies, and maintenance of associated disposal records and logs.
• Provide support to senior clinical research staff and management and perform other related duties as assigned.

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.

Everyone Matters

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.

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.