Top 15 Clinical research assistant Jobs in Deland Fl

Clinical Research Coordinator I
Velocity Clinical Research, Inc. —Edgewater, FL
- Full-time
- English
- Mid-level
- Ability to sit for extended periods
- Paid holidays
- Health insurance
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Travel Clinical Research Coordinator
Alcanza Clinical Research —Lake Mary, FL
- Full-time
- Spanish
- LVN
- HIPAA
- Health savings account
- Disability insurance
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Clinical Research Technician I, Early Phase Clinical Research - Daytona Beach, FL
Fortrea —Daytona Beach, FL
- Full-time
- CPR Certification
- BLS Certification
- Office
- Disability insurance
- Health insurance
Psychometric Rater
Alcanza Clinical Research —DeLand, FL
- Full-time
- Spanish
- BLS Certification
- HIPAA
- Health savings account
- Disability insurance
Quick Apply
9d
Special Projects Coordinator - Clinical Assistant to the Medical Director
County of Volusia —Holly Hill, FL
- $31.62 an hour
- Full-time
- HIPAA
- Mid-level
- Math
Clinical Research Nurse, Early Phase Clinical Trials - Daytona Beach, FL (On-Site)
Fortrea —Daytona Beach, FL
- Full-time
- CPR Certification
- Nursing
- Bachelor of Science
- Disability insurance
- Health insurance
Special Projects Coordinator - Clinical Assistant to the Medical Director
Volusia County, FL —Holly Hill, FL
- $65,769.60 a year
- Full-time
- Management
- Writing skills
- HIPAA
- Paid holidays
- Disability insurance
Senior Clinical Site Director
Fortrea —Daytona Beach, FL
- Full-time
- Clean driving record
- Bachelor of Science
- Clinic
Forensic Pediatrics and Child Protection - Clinical Assistant/Associate Professor
University of Florida —Volusia, FL
- Background check
- Medicine
- University
Paramedic / Daytona Beach, FL (On-Site)
Fortrea —Daytona Beach, FL
- Full-time
- CPR Certification
- BLS Certification
- Mid-level
- Disability insurance
- Health insurance
3d

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Clinical Research Assistant II
The Ohio State University Wexner Medical Center —Columbus, OH
Bachelor’s Degree in biological sciences, health sciences, or medical field, or equivalent combination of education experience; experience in research capacity…
3d
Clinical Research Assistant
The Ohio State University Wexner Medical Center —Columbus, OH
To provide assistance in support of clinical research studies; assists with implementation and coordination of studies; participates in recruitment of study.
2d

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Clinical Research Coordinator I

Velocity Clinical Research, Inc. -
Edgewater, FL

Quick Apply

Job Details

Full-time

Benefits

Paid holidays
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching

Qualifications

Injectable medication administration
Phone communication
English
Phlebotomy specimen handling
Fax machines
Multi-line phone systems
Productivity software
Faxing
Medical terminology
Delegation
Client interaction via phone calls

Full Job Description

Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.

As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.

Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.

Summary:

The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs.

Duties/Responsibilities:

Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs
Coordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.
Implement research and administrative strategies to successfully manage assigned protocols.
Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.
Apply good documentation practices when collecting and correcting data, transferring data to sponsor/CRO data capture systems, and resolving queries
Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information
Ensure patient safety is upheld and all adverse events, serious adverse events, and adverse events of special interest are followed and reported in accordance with the protocol and Velocity SOPs.
Ensure all data is entered into the sponsor's data portal and all queries are resolved in a timely manner
Ensure staff are delegated and trained appropriately and documented
Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.
Evaluate potential subjects for participation in clinical trials including phone and in person pre screens.
Execute recruitment strategies defined by Clinical Research Team
Understand key timelines, endpoints, required vendors, and patient population for each assigned protocol.
Perform clinical duties (e.g. drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope
Promote respect for cultural diversity and conventions with all individuals.

Education/Experience:

Bachelor’s degree with 1 year of relevant experience in the life science industry OR
Associate’s degree with 2 years of relevant experience in the life science industry OR
High School Graduate and/or technical degre with minimum of 3 years relevant experience in the
life science industry

Required Licenses/Certifications:

Phlebotomy if applicable and required by state law
Intramuscular dose administration and preparation if applicable and required by state law

Required Skills:

Demonstrated knowledge of medical terminology
Demonstrated ability in the use of the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
Demonstrated bility to work in a fast-paced environment
Demonstrated verbal, written, and organizational skills
Demonstrated interpersonal and communication skills
Demonstrated ability to work as a team player
Demonstrated ability to read, write, and speak English
Demonstrated ability to multi-task
Demonstrated ability to follow written guidelines
Demonstrated ability to work independently, plan and prioritize with some guidance
Demonstrated ability to be flexible/adapt as daily schedule may change rapidly
Must be detail oriented
Demonstrated problem solving and strategic decision making ability.
Proficient ability to accept individual responsibility for actions taken and demonstrate professionalism when judged, critiqued and/or praised.

Required Physical Abilites:

Sit or stand for long periods of time
Travel locally and nationally
Communicate in person and by a telephone
Limited walking required
Limited to lifting up to 30 pounds

NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required. Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change. All employees are expected to perform their duties within their ability as required by the job and/or as requested by management.

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Refine Your Search

clinical research assistant jobs in deland fl

Clinical Research Coordinator I

Travel Clinical Research Coordinator

Clinical Research Technician I, Early Phase Clinical Research - Daytona Beach, FL

Psychometric Rater

Special Projects Coordinator - Clinical Assistant to the Medical Director

Clinical Research Nurse, Early Phase Clinical Trials - Daytona Beach, FL (On-Site)

Special Projects Coordinator - Clinical Assistant to the Medical Director

Senior Clinical Site Director

Forensic Pediatrics and Child Protection - Clinical Assistant/Associate Professor

Paramedic / Daytona Beach, FL (On-Site)

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