Job detail

Clinical Research Coordinator

ALS

#SOP #Clinical Research #Principal Investigator #Life Sciences #Clinical Protocols #Clinical Testing #Good Clinical Practices #Clinical Management #Study Coordinator

Quick overview

The coordinator plans and develops safety and efficacy research studies under the supervision of a Principal Investigator. They oversee day-to-day clinical activities, supervise research assistants, and manage study workflow and reporting.

Requirements summary

A Bachelor of Science or Arts degree in life sciences is preferred, or 1-2 years of clinical industry experience. Candidates must be physically able to stand for long periods and lift up to 50 pounds.

bachelor degreeInventory ManagementTeam SupervisionData MonitoringSubject RecruitmentStudy CoordinationGood Clinical PracticesClinical TestingClinical Protocol Implementation

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.
About the role ALS global company, is a leader in the field of clinical testing with an opening for full-time Clinical Research Coordinator (CRC) in Phoenix, AZ.
The successful candidate will join a team that provides clinical testing services to many of the world's best-known consumer product companies.
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.
About you: Bachelor of Science or Arts degree in life sciences preferred.
1 – 2 years’ experience in clinical industry experience (substitute for BS or BA).
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 50 pounds and occasionally lift and/or move heavier loads with assistance Must be able to interact and communicate effectively with panelist 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 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.
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 resume & cover letter that best demonstrate your motivation and ability to meet the requirements of this role.
ALS is a global leader in testing, providing comprehensive testing solutions to clients in a wide range of industries around the world.
Using advanced technologies and innovative methods, we help our clients leverage data-driven insights for a safer and healthier world.
Our people are the heart of our business, driving testing solutions and innovations to solve complex challenges and create lasting value for our clients.
But most importantly, our people care – for each other and for the work we do.
With over 20,000 team members across 70 countries, you’ll be part of a global network.
Learn more about what makes our workplace great here.
Didn’t see the right job for you today?
We'd still love to hear from you.
With a team of more than 20,000 employees across 70 countries, it takes all kinds of skills and expertise to make a company like ours thrive – and not all of them are in labs!
We’re all about people – so show us who you are and why you're passionate about working with us by submitting your resume, and we’ll keep it on file for future opportunities.
Want to know more?
Check out our careers page to find out about the benefits of joining our team, and don’t forget to follow us on LinkedIn for the latest updates!

Clinical Research Coordinator

Quick overview

Requirements summary

Job description

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