Clinical Research Coordinator

ALS Global • Torrance, CA

1d • Onsite

About The Position

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. Clinical Research Coordinator 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. About the role RCTS, an ALS global company, is a leader in the field of clinical testing with an opening for full-time Clinical Research Coordinator (CRTs) in Torrance, CA. The successful candidate will join a team that provides clinical testing services to many of the world's best-known consumer product companies. Hourly Rate: $24-$26 The Study Coordinator will be responsible for: 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. Duties include but not limited to: The Study Coordinator has the following duties: 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 assigned.

Requirements

• Bachelor of Science or Arts degree in life sciences preferred.
• 1 – 2 years’ experience in clinical industry experience (substitute for BS or BA).
• 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 50 pounds and occasionally lift and/or move heavier loads with assistance
• Must be able to interact and communicate effectively with panelist
• 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.

Responsibilities

• 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 assigned.

Benefits

• 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)

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level