Brainsport Clinical Research Coordinator

General Information

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Work Location: Los Angeles, USA

Onsite or Remote

Flexible Hybrid

Work Schedule

Monday-Friday, 8:00am-5:00pm

Posted Date

06/18/2024

Salary Range: $32.65 - 52.53 Hourly

Employment Type

2 - Staff: Career

Duration

Indefinite

Job #

17409

Primary Duties and Responsibilities

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In this position, you will serve as the lead Clinical Research Coordinator (CRC) for the BrainSPORT team. You will provide clinical research coordination for the CARE4Kids U54 grant and administrative support as needed. You will also oversee volunteers and work with junior research coordinators to run study protocol. In addition, you will help with recruitment efforts and running study protocol.

Salary Range: $33.63 - $54.11 Hourly

Job Qualifications

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Required:

• Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.

• Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and costeffectiveness.

• Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment.

• Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.

• Ability to respond to situations in an appropriate and professional manner.

• Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines.

• Ability to be flexible in handling work delegated by more than one individual.

• Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications.

• Ability to handle confidential material information with judgement and discretion.

• Working knowledge of the clinical research regulatory framework and institutional requirements.

• Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets.

• Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.

• Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc.

Preferred:

• Bachelor's degree or 1-3 years of previous study coordination or clinical research coordination experience.