Clinical Research Associate Job at Kelly Services, Van Nuys, CA

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  • Kelly Services
  • Van Nuys, CA

Job Description

Clinical Research Associate

  • Location: Remote – Home based

  • Opportunity: 3–6-month full time contract with potential to extend or convert to direct hire with our CRO client

  • Salary depends on location and years of experience: Range target is $35.00-45.00 w-2 hourly

Kelly Science and Clinical is hiring a Clinical Research Associate for our client who is a Diagnostic CRO. This is an opportunity to work with a growing clinical research company and offers the ability for growth within your career goals as the company expands nationwide. This need will start off as a contract opportunity that has high potential to extend or possibly convert to permanent in the future.

The Clinical Research Associate will ensure clinical trials are completed on-time, according to the protocol, and to keep clients and sites informed throughout the process.

Responsibilities

  • Manage diagnostic clinical studies

  • Develop and manage the protocol, case report form, budget/contract negotiation and regulatory document management

  • Assist clinical sites with IRB submission/documentation, as needed

  • Setup and keep Diagnostica, their own remote clinical trial management system, up to date

  • Monitor clinical studies.

  • Develop monitoring plans, identify issues, and resolve queries, ensure site regulatory binders are compliant

  • Manage site relationships by helping with study startup, answer questions during the study, ensure timely payments and close out activities

  • Ability to travel Nationwide depending on the study load and expectations (10-50% expectations)

Skills & Requirements

  • A minimum of 4 years’ experience in the clinical research industry supporting clinical studies or clinical operations currently or recently

  • Prefer at least 1-2 years clinical research monitoring experience

  • Must have strong understanding of clinical trial regulatory and compliance processes

  • Understanding of regulations for FDA and Sponsor trial auditing

  • Strong ability to research data and identify issues or potential red flags in a study

  • Ability to learn quickly and expand knowledge into trial processes

  • Diagnostic clinical study experience or lab diagnostic experience preferred

  • Knowledge of accepted good clinical research practice (GCP) and procedures

  • Excellent organizational, time management, budget management, and problem-solving skills

  • Hustle: Comfortable in a fast-paced small company environment

  • SOCRA CRA certification or will help you apply if not certified already once hired and through training

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Job Tags

Hourly pay, Holiday work, Permanent employment, Full time, Contract work, Temporary work, Local area, Remote job, Work from home,

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