Job Description

Clinical Research Associate

• Location: Remote – Home based

• Opportunity: Contract for 3-6 months with high potential to renew

• Hours: Hours may flex from 30-40 a week depending on study load

• Travel: Depends on the study need and location of home office but average would be between 30-50% travel nationwide

• Salary depends on location and years of experience: Range is between $50.00 - $55.00 an hour w-2

Kelly Science and Clinical is hiring a Clinical Research Associate for our client who is a Diagnostic CRO. This is a contract opportunity to work directly with a growing clinical research CRO that could offer the ability for growth within your career goals as the company expands nationwide. This will start as a 3-6 month contract with high possibility for extending the contract length. This may be flexible with weekly hours between 30-40 a week depending on the workload. We are only moving forward with candidates who have the ability to commit 40 hours a week and at least 6 month dedication to support the study needs.

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. The CRA will need to have experience monitoring IVD studies and at least two years of proven clinical research site monitoring for a CRO or sponsor client in the past.

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 2 years clinical research monitoring experience with a CRO, biotech, or pharmaceutical company required

• Diagnostic clinical study experience or lab diagnostic experience (IVD monitoring experience requested)

• 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 preferred

• Must have home office set up and ability to travel nationwide up to average of 50% at times

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.

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