**Overview** **Clinical** **Study Coordinator I** **Imagine your future with us** At ALS, we encourage you to dream big. When you join ALS, you join a purpose and values-driven team that empowers you to innovate, create, and thrive. Our global team turns up each day with passion and commitment to do amazing things, always challenging our thinking to find ways to solve some of the world’s most complex problems for a safer, healthier world. **Responsibilities** **About the role** The Clinical Study Coordinator I plans, develops and coordinates the safety and efficacy research studies under the supervision of the Principal Investigator and in accordance to protocol, company SOP’s and Good Clinical Practices. Successful candidates will join a fast paced, positive team with a reputation for excellence in clinical testing that is part of a larger global organization of over 17,000 employees in over 60 countries. At ALS you will join a team that provides clinical testing services to many of the world's leading cosmetic, consumer product and pharmaceutical companies. **Duties include but not limited to:** As a Study Coordinator 1 you will be responsible for critical aspects of clinical testing, including: + Participates and coordinates the planning, development and implementation of clinical protocols, logistical procedures and operating systems in accordance with parameters set out by the study sponsor and Principal Investigator. + Supervises, evaluates and coordinates the activities of a team of Clinical Research Assistants; ensures that all clinical activities are carried out in accordance with Company SOP's and guidelines of Good Clinical Practices. + Oversees the planning, scheduling and carrying out of day-to-day clinical activities, maximizing on study workflow, and associated availability of research subjects. + Works closely with Recruitment Department ensuring specific research subject entrance criteria is observed prior to conducting study. + Monitors test subjects’ response to treatment and communicates study data and results to investigators in a timely fashion. + Works in conjunction with Clinical Management on generation of protocols, interim reports and final reports for Company sponsors. + Order and maintain inventory of laboratory supplies. + Other duties as may be required. **About you:** + High School diploma or equivalent + Bachelor of Science or Arts degree in life sciences preferred. + 1 – 2 years’ experience in clinical industry experience (substitute for BS or BA). This position is the best fit for someone who is looking to begin a career in the clinical research profession and who would like to develop their experience and skills to move up within our company. Strong oral, written, and qualitative skills are a plus. **Working conditions:** + Sitting and/or standing for extended periods of time, up to eight (8) hours per business day + Must be able to stand, bend, push, pull, stoop and crouch frequently while performing the duties of this position + Must be able to lift (with both hands) and/or move up to 20 pounds and occasionally lift and/or move heavier loads with assistance + Must be able to interact and communicate effectively with panelists **Qualifications** **Working at ALS** Our people are our most valuable asset and drive our success at ALS. We are a diverse community of dedicated professionals united by our passion to make a difference in the world. We reward excellence and uphold our values in our work and how we treat each other. At ALS, you’ll be supported to expand your skills and develop new ones so you can reach your full potential. We invest in our people with a range of programs and provide opportunities across the company, giving our people scope to grow diverse careers and develop as leaders. We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and the communities where we work. Our benefits include: + Comprehensive benefit package including medical, dental, and vision coverage, life and disability insurance, retirement plan with company match, employee assistance and wellness programs, access to company perks + Annual structured wage increases + PTO + Business support for education or training after 9 months with the company + Learning & development opportunities (unlimited access to e-learnings and more) **About ALS** ALS is a global leader in scientific testing, providing comprehensive testing solutions to clients in more than 60 countries across a wide range of industries, including environment, food and beverage, mining, personal care, pharmaceutical, healthcare and equipment reliability. Using state-of-the-art technologies and innovative methodologies, our dedicated international teams deliver the highest-quality testing services and personalized solutions supported by local expertise. We help our clients leverage the power of data-driven insights for a safer and healthier world. **Everyone matters** ALS is proud to be an equal opportunity employer committed to achieving and maintaining a workforce which reflects and affirms the diversity of our society ALS is a VEVRAA Federal Contractor. EOE AA Minority, Female, Veteran, Individuals with Disabilities. Click Here to view the EEO is the Law poster Click Here to view the FMLA Law poster Click Here to view the EPPA Law Poster Click Here to view the Pay Transparency Provision Click Here to view company E-Verify Participation Poster ALS also welcomes applications from people with all levels of ability. Accommodation is available on request for candidates taking part in all aspects of the selection process. **Location** _US-AZ-Phoenix_ **Job ID** _2025-11038_ **\# Positions** _1_ **Posted Date** _1 day ago_ _(2/11/2025 6:01 PM)_ **Category** _Scientific_ **Type** _Regular Full-Time_ **OC** _ALSENV_