Top 183 Clinical research assistant Jobs in Fort Lauderdale Fl

Clinical Research Nurse - Per diem
Quotient Sciences —Miami, FL
- Part-time
- 18 years or older
- Spanish
- Nursing
Quick Apply
10d
Clinical Research Coordinator
Indago Research & Health Center, Inc —Miami Lakes, FL
- $23 - $30 an hour
- Weekends as needed
- Background check
- Spanish
- HIPAA
- Paid holidays
- Disability insurance
Quick Apply
2d
Site Manager – Clinical Research (Neuroscience & Psychedelics)
Segal Trials —Lauderhill, FL
- Full-time
- Psychiatry
- 3 years
- Supervising experience
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Assistant / Medical Assistant
CenExel Clinical Research —Hollywood, FL
- Full-time
- Background check
- Spanish
- Vital signs
- Health savings account
- Health insurance
Quick Apply
Regulatory Coordinator
CenExel Clinical Research —Hollywood, FL
- Overtime
- Background check
- Microsoft Excel
- Psychiatry
- Health savings account
- Health insurance
Quick Apply
Medical Assistant (Clinical Research)
Research Centers of America —Hollywood, FL
- Spanish
- Computer literacy
- Writing skills
- Health insurance
- Dental insurance
Quick Apply
Research Assistant
Evolution Research Group —Delray Beach, FL
- $45,000 - $50,000 a year
- Full-time
- Office
- High school diploma or GED
- Neurology
- Health insurance
- Dental insurance
Quick Apply
5d
Clinical Research Associate
Biorasi LLC —Aventura, FL
- From $103,000 a year
- Email
- Hybrid work
- Mid-level
- Bachelor's degree
- 1 year
Quick Apply
Clinical Research Coordinator
Flourish Research —Boca Raton, FL
- $28 - $35 a year
- Full-time
- Vital signs
- HIPAA
- Mid-level
- Paid holidays
- Disability insurance
Quick Apply
5d
Clinical Research Assistant (experienced required)
FWD Clinical Research —Tamarac, FL
- $17 - $24 an hour
- Part-time
- Bilingual
- Patient monitoring
- Inventory management
Quick Apply
5d
Research Associate, Oncology Research, FT,8A-4:30P
Baptist Health South Florida —Boca Raton, FL
- $58,494.88 - $76,043.34 a year
- Full-time
- 5 years
- Analysis skills
- Math
- Wellness program
- Health insurance
Quality Assurance Coordinator (Clinical Research)
Research Centers of America —Hollywood, FL
- Full-time
- Background check
- Spanish
- Psychiatry
- Health savings account
- Health insurance
Quick Apply
Clinical Research Coordinator
Segal Institute for Clinical Research —Lauderhill, FL
- Full-time
- Vital signs
- Psychiatry
- Addiction Medicine
- Health insurance
- Dental insurance
Quick Apply
2d
Patient Recruitment Manager (Clinical Research)
CenExel Clinical Research —Hollywood, FL
- Full-time
- Background check
- Spanish
- Management
- Health savings account
- Health insurance
Quick Apply
Clinical Research Coordinator
Segal Institute for Clinical Research —North Miami, FL
- Full-time
- Bilingual
- Vital signs
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
2d
Clinical Research Coordinator 1
University of Miami —Boca Raton, FL
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Bachelor's degree
- Health insurance
- Dental insurance
Research Associate 1
University of Miami —Miami, FL
- Full-time
- No experience needed
- Bachelor's degree
- Psychology
- Health insurance
- Dental insurance
Research Assistant
Flourish Research —North Miami, FL
- $21 - $23 a year
- Full-time
- Vital signs
- Computer literacy
- Bachelor's degree
- Paid holidays
- Disability insurance
Quick Apply
Clinical Research Coordinator
BRCR Global —Tamarac, FL
- Full-time
- Mid-level
- 401(k)
Quick Apply
5d
Research Assistant, Protocol Support Laboratory
Baptist Health Herbert Wertheim Cancer Institute —Miami, FL
- $21.24 - $25.70 an hour
- Computer literacy
- BLS Certification
- Quality control
- Wellness program
- Health insurance

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Clinical Research Nurse - Per diem

Quotient Sciences -
Miami, FL

Quick Apply

Job Details

Part-time
10 days ago

Qualifications

Microsoft Outlook
RN License
ACLS Certification

Full Job Description

Quotient Sciences: Molecule to Cure. Fast.
Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development, clinical pharmacology, clinical trials, and commercial product manufacturing.
Our proprietary and disruptive platform – “Translational Pharmaceutics®” – integrates Drug Product Manufacturing and Clinical Testing to eliminate silos in the drug development process. This in turn reduces costs, improves outcomes, and significantly accelerates drug development times.

Why join us:
Because every day counts when bringing new medicines to patients. Our 1,000+ experts across the US, UK, and beyond are united by science, agility, and a culture that turns ideas into impact—fast.

The Role

Responsible for coordinating, supervising and monitoring study activities, following adverse events and administering study medications
To comply & adhere to GCP guidelines and regulations as required of this role
To ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standards
To ensure subject safety at all times

Main Tasks and Responsibilities

Responsible for administering study medication to study participants
Familiar with intravenous infusion techniques including pumps
Responsible for supervising staff and study events on the unit according to protocol requirements. Responsible for making staff adjustments during absences or others unanticipated work circumstances
Responsible for monitoring study schedules and reviewing study activities as they progress
Responsible for reviewing, recording and following adverse events
Responsible for confirming that a complete screening chart containing informed consents, lab results and Investigator approval is available on the day of admission for every admitted subject
Responsible for monitoring clinical results, compliance, and/or safety issues which would trigger the exclusion or discontinuation of a participant
Ability to effectively interact with pharmaceutical company representatives (monitors) and clinical research organizations (CRO) in response to queries during the course of the research study
Participates in key study meetings- SIV, Clinical Kick-off, paperwork review, dummy run and as required
Assures that all necessary source documents are available on the unit on a timely basis
Reviews study source documents for completion
Familiarity with crash cart emergency procedures. Responds to medical emergencies in clinic and to adverse events requiring urgent attention
Assists with other nursing duties as assigned
Additional Tasks/responsibilities
Assists with new employee (regular and per diem) training by providing orientation to general study procedures and responsibilities

Job Demands

The job may involve the following:

Very high concentration of work
Strict and tight deadlines
Having to juggle a range of tasks/issues simultaneously
Working in a hazardous environment with high requirement to follow safety procedures
Working outside normal working hours
Needing to respond to client demands

The Candidate

BSN or RN with experience preferably within a critical care setting and/ or clinical research environment
Current/valid Florida nursing license
Current Advanced Cardiac Life Support (ACLS) certification
Fluent in English/Spanish preferred
Computer proficient in Microsoft Office products (e.g. Outlook, Word)
High attention to details
Excellent communication and interpersonal skills

This Job Description is designed to summarize responsibilities, assist in benchmarking performance, and provide information for job applicants. It is by no means exhaustive and is not intended to restrict a job holder’s development or level of performance.
#INDHP

Application Requirements
When applying for a position with Quotient Sciences to be able to work in our organization you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined.
Our Commitment to Diversity, Equity and Inclusion
Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today.
Specifically we will not discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws.
This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.

Quick Apply

Refine Your Search

clinical research assistant jobs in fort lauderdale fl

Clinical Research Nurse - Per diem

Clinical Research Coordinator

Site Manager – Clinical Research (Neuroscience & Psychedelics)

Clinical Research Assistant / Medical Assistant

Regulatory Coordinator

Medical Assistant (Clinical Research)

Research Assistant

Clinical Research Associate

Clinical Research Coordinator

Clinical Research Assistant (experienced required)

Research Associate, Oncology Research, FT,8A-4:30P

Quality Assurance Coordinator (Clinical Research)

Clinical Research Coordinator

Patient Recruitment Manager (Clinical Research)

Clinical Research Coordinator

Clinical Research Coordinator 1

Research Associate 1

Research Assistant

Clinical Research Coordinator

Research Assistant, Protocol Support Laboratory

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