Clinical Research Coordinator

Reliance Clinical Testing Services, Inc.; Torrance (CA); On-site; USD 33,000 - 36,000; Full time

Benefits offered by this job

Medical, dental, and vision coverage

Retirement plan with company match

PTO

Education/training support after 9 mo.

Learning & development opportunities

Job summary

ALS in Torrance, CA is seeking a full-time Clinical Research Coordinator to support safety and efficacy studies under the PI, following protocol, SOPs and GCP. The role involves coordinating clinical protocols, supervising a team, and ensuring study workflow efficiency on-site.

Applicants should have a BS/BA in life sciences and 1–2 years of clinical industry experience. Competitive hourly rate and comprehensive benefits offered in a collaborative environment.

Qualifications

• Bachelor of Science or Arts degree in life sciences preferred.
• 1–2 years’ experience in clinical industry experience (substitute for BS or BA).

Responsibilities

• Plan and coordinate safety and efficacy studies under the PI following protocol, SOPs, and GCP.
• Coordinate planning and implementation of clinical protocols and procedures per sponsor and PI.
• Supervise Clinical Research Assistants and ensure compliance with GCP.
• Oversee day-to-day clinical activities and study workflow to maximize subject availability.
• Collaborate with Recruitment to ensure entrance criteria are observed.
• Monitor subjects’ responses and report data to investigators promptly.
• Assist in generation of protocols, interim and final reports for sponsors.
• Order and maintain inventory of laboratory supplies.
• Perform other duties as assigned.

Education

Bachelor of Science or Arts degree in life sciences

Job description

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.

Hourly Rate: $24-$26

Responsibilities

Duties include but not limited to:

• 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.
• 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.

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).

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.

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 are 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.

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.

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.

EEO and Diversity

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.

Qualified candidates will be considered without regard to race, colour, religion, nationality, 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.

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.