Job description

Research Assistant

Brief Description:

A Research Assistant performs a variety of clinical study activities to assist the Clinical Research Coordinator (CRC) and the Clinical Trial Investigator in the conduct of a clinical study. A Research Assistant is responsible for learning and performing all the basic activities to conduct a clinical study. A Research Assistant does not have any management responsibilities.

Qualifications/Job Requirements:

Ability to function independently.

Attentiveness to details.

Multi-tasking capability.

Potential to manage assigned projects.

Good interpersonal, written, and verbal communication skills.

Ability to meet a flexible work schedule.

Motivated self starter with the ability to work independently and manage a variety of projects simultaneously.

Research Assistant Responsibilities are to Assist the CRC in the following:

To conduct the clinical study according to FDA regulation and guidelines

To design and maintain organizational tools to conduct the study accurately and in compliance with GCP.

To ensure the safety and welfare of the study participants.

To be knowledgeable of the Sponsor’s protocol so that all the study activities are completed correctly and completely.

To assist medical investigators in implementing the protocol.

To recruit and screen the potential study participants according the protocol’s inclusion and exclusion criteria.

IF SPECIFICALLY TRAINED - To obtain proper written informed consent from each study participant prior to participation in the study.

To schedule study participants’ visits and during the study participants’ visit perform defined activities of the study completely and accurately.

To report all serious adverse events to the Investigator and Site Director/Director of Operations.

To maintain adequate and accurate case histories for each study participant that records all observations and data during the study.

To complete the Source Documents/Case Report Forms for the study accurately and completely.

IF SPECIFICALLY TRAINED - To assign study participant numbers and maintain accurate and complete records of the receipt, dispensation,

and return of all clinical supplies. All discrepancies are noted and explained.

To maintain all required documentation in orderly manner and provide to data coordinator for filing.

To maintain records of study participants’ status in the study.

IF SPECIFICALLY TRAINED - To communicate with the Sponsor regarding study activities as necessary.

IF SPECIFICALLY TRAINED - To meet with the Sponsor’s representatives to discuss the conduct of the study and review study data.

To use computer applications to enhance the efficiency of the workflow and study activities.

Job Type: Full-time

Pay: $20.00 - $26.00 per hour

Benefits:

• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday

COVID-19 considerations:
We clean and sanitize our facilities nightly and provide PPD equipment to staff and interacting with subjects.

Ability to commute/relocate:

• Lake Worth Beach, FL 33460: Reliably commute or planning to relocate before starting work (Required)

Experience:

• Clinical trials: 1 year (Preferred)
• Research: 1 year (Preferred)

Language:

• Spanish & English (Required)

Work Location: In person

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