Clinical Research Coordinator — Growth, PTO & Training

Reliance Clinical Testing Services, Inc.; Torrance (CA); Presencial; USD 33 000 - 36 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Medical, dental, and vision coverage

Retirement plan with company match

PTO

Education/training support after 9 mo.

Learning & development opportunities

Resumo da oferta

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.

Qualificações

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

Responsabilidades

• 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.

Formação académica

Bachelor of Science or Arts degree in life sciences

Descrição da oferta de emprego

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.