Clinical Research Coordinator

ALS; Torrance (CA); On-site; USD 33,000 - 36,000; Full time

Job summary

ALS is seeking a Clinical Research Coordinator in Torrance, CA to join our global team conducting safety and efficacy studies under the supervision of the Principal Investigator.

The role involves planning, coordinating protocols, supervising research assistants, coordinating patient recruitment, monitoring data, and generating reports; must have life sciences BS/BA and 1–2 years clinical experience. This is a full-time position in a dynamic, values-driven environment.

Qualifications

• BS/BA degree in life sciences preferred.
• 1-2 years' clinical industry experience.

Responsibilities

• Plans, develops, and coordinates safety and efficacy research studies under PI supervision.
• Supervises Clinical Research Assistants and ensures compliance with SOPs and GCP.
• Oversees day-to-day clinical activities and study workflow availability of subjects.
• Collaborates with Recruitment to verify entrance criteria before studies.
• Monitors subjects' response to treatment and reports study data to investigators.
• Assists management in protocol development, interim and final reports.
• Orders and maintains inventory of laboratory supplies.
• Other duties as assigned.

Skills

Clinical research coordination

Team supervision

Education

BS/BA Life Sciences

Job description

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.

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.

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

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.

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.

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.