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Clinical Research Assistant (experienced required)

FWD Clinical Research
Spring Hill, FL

Quick Apply

Job Details

Part-time
$17 - $25 an hour

Qualifications

Collaborate with healthcare professionals
Research project management
Computer operation
Clinical research
Microsoft Office
High school diploma or GED
Project management
Bachelor's degree
Organizational skills
Clinical trials
Managing projects

Full Job Description

Qualifications

1+ year of experience in Medical\Healthcare setting
Strong Project Management skills
Strong organizational skills; able to manage multiple projects at once.
Bilingual is a plus
Proven ability to work independently with low supervision
Strong understanding of computer technological skills and programs such as MS Office programs.
Excellent interpersonal skills when collaborating with clinicians, patients, administrators, investigators, sponsors, etc.

Education

High School Diploma or Equivilent
Basic Knowledge of Medical Terminology
Any healthcare training is a plus (NOT REQUIRED)

The Clinical Research Assistant supports investigators and research staff in the successful conduct of clinical trials while ensuring compliance with protocol requirements, Good Clinical Practice (GCP), sponsor guidelines, and regulatory standards.

Key Responsibilities

Assist investigators and research coordinators with the day-to-day management of clinical trials.
Perform study-related procedures and assessments as delegated and permitted by protocol and training.
Enter clinical trial data accurately and timely into Electronic Data Capture (EDC) systems and assist with Clinical Trial Management System (CTMS) tracking.
Prepare, organize, and maintain study binders, source documents, and essential regulatory files.
Schedule and coordinate study visits, patient appointments, and study-related procedures.
Assist with patient recruitment, pre-screening activities, and participant retention efforts to meet enrollment goals.
Process laboratory specimens, label samples, complete requisitions, and prepare shipments in accordance with protocol requirements and applicable shipping regulations.
Assist with adverse event, serious adverse event, and protocol deviation documentation and reporting as directed.
Support implementation of protocol amendments and study updates.
Generate reports and provide administrative support for study tracking, monitoring visits, audits, and meetings.
Communicate professionally with study participants, investigators, sponsors, CROs, vendors, and internal staff.
Maintain strict confidentiality of patient health information and sponsor proprietary information.
Ensure participant safety by promptly communicating any safety concerns to the research team.
Understand study timelines, visit schedules, endpoints, and protocol requirements for assigned studies.
Perform clinical procedures within training and scope of responsibility, including phlebotomy, ECGs, vital signs, specimen processing, and investigational product accountability, as applicable.
Assist with monitoring visits, sponsor visits, audits, investigator meetings, and study closeout activities.
Support office operations, including reception duties, supply inventory management, filing, and administrative organization.
Prepare meeting materials, reports, and action items for monthly research and operational meetings.
Contribute to the successful execution of assigned studies by maintaining organization, accuracy, and compliance throughout the study lifecycle.

Job Type: Part-time

Pay: $17.00 - $25.00 per hour

Education:

Bachelor's (Preferred)

Experience:

Clinical research: 1 year (Preferred)

Work Location: In person

Quick Apply

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Fwd jobs

Clinical Research Assistant (experienced required)

Midwest Organizing Director

Operations Coordinator

Project Management Director

Omnichannel Strategy Director

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