Top 21 Clinical research Jobs in Melbourne, Fl

Clinical Research Coordinator (part-time)
Thermo Fisher Scientific —Melbourne, FL
- Part-time
- English
- Mid-level
- Office
Clinical Research Coordinator
Tandem Intermediate LLC —Melbourne, FL
- Mid-level
- Databases
- Bachelor's degree
Quick Apply
Research Lead
Kalogon, Inc. —Melbourne, FL
- $60,000 - $120,000 a year
- Email
- Doctoral degree
- Office
- Master's degree
- 401(k) matching
Quick Apply
Licensed Clinical Social Worker - Temp
Decypher —Patrick Space Force Base, FL
- Temporary
- Mid-level
- Ability to sit for extended periods
- Ability to stand for extended periods
Quick Apply
Clinical Exercise Physiologist
Carda Health —United States
- $30 - $36 an hour
- Contract
- Remote
- Background check
- Spanish
- Mid-level
Quick Apply
HL7 Data Analyst
VITL —United States
- $110,000 - $115,000 a year
- Email
- 5 years
- Salesforce
- Mid-level
- Health savings account
- Disability insurance
Quick Apply
2d
Special Agent: Healthcare Services/Medical Background
Federal Bureau of Investigation —United States
- $103,326 - $133,200 a year
- Full-time
- Mid-level
- Bachelor's degree
- Travel
11d
Head of Clinical Operations (Oncology)
Kaztronix —United States
- Remote
- 11+ years
- Business development
- Bachelor's degree
Quick Apply
MedTech Part Time Clinical Consultant – San Francisco, CA
IQVIA —United States
- $85 an hour
- Part-time
- RN License
- Mid-level
- 3 years

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Clinical Research Coordinator (part-time)
Thermo Fisher Scientific —Melbourne, FL
Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken…
Clinical Research Coordinator
Tandem Intermediate LLC —Melbourne, FL
Education: Bachelor’s degree in a related field. Preferred Credentials: Medical certification or licensure (e.g., MS, LPN, RN).
Quick Apply

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Clinical Research Coordinator (part-time)

Thermo Fisher Scientific -
Melbourne, FL

Apply Now

Job Details

Part-time

Qualifications

Research project team leadership
Record keeping
Computer operation
Staff supervision
Document review (document control)
Operating systems
English
Mid-level
Programming languages
Data management
Computer hardware
Driving
Managing clinical research teams
Mentoring
Research compliance clinical trial records management
Organizational skills
Clinical trial standard operating procedures
Implementing research protocols
Patient recruitment
Budgeting
Project leadership
Grammar Experience
Leadership
Standard operating procedures (SOPs)
Project planning phase
Team motivation (leadership skill)
Communication skills
Project stakeholder communication
File organization
Research compliance audit records management

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join us as Clinical Research Coordinator - And manage the day-to-day operations of our clinical trials.

What You’ll Do:

Conduct multiple ongoing clinical trials, of varying size and complexity, involving patients or healthy volunteers/subjects.
Complete all paperwork required to capture all data as specified by a study protocol, and for ensuring subject safety, understanding, and cooperation during the study process. Interact with the research site team and other interdepartmental staff.
Engage in the entire site operations process, which includes recruitment, enrollment and retention of study participants.
May act as primary or lead CRC on certain studies, taking the overall responsibility thereof at the site, while maintaining communication and updates with site team, liaising with monitors and other stakeholders.

Education and Experience:

Relevant formal academic / vocational qualification and / or previous experience that provides the knowledge, skills and abilities to perform the job (comparable t 0 to 5 years). 1+ year of leadership responsibility.

In some cases, an equivalency consisting of a combination of appropriate education, training and / or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

Fundamental communication and interpersonal skills with the ability to manage, motivate and mentor staff
Strong organization skills with ability to handle multiple tasks simultaneously, meet rigorous timelines and work effectively in stressful situations
Understanding of budgets, project planning and performance metrics
Strong English and grammar skills, second language a plus, but not required.
Sound knowledge of organization's archival processes and systems (hardware, software, applications, operating systems, basic programming languages, etc.), SOPs and training requirements
Ability to manage the day-to-day operation of Records Management file rooms including but not limited to document control, security and audit preparedness

Working Conditions and Environment:

Work is performed in an office environment with exposure to electrical office equipment.
Frequently drives to site locations with possible travel both domestic and international for sponsor or industry related meetings.

Physical Requirements:

Frequently stationary for 6-8 hours per day.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
Moderate mobility required.
Occasional crouching, stooping, bending and twisting of upper body and neck.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
Frequently interacting with others, relates sensitive information to diverse groups both internally & externally.
Ability to apply basic principles to solve conceptual issues.
Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.
Regular and consistent attendance.

Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthrough.

Apply Now

Refine Your Search

clinical research jobs in melbourne, fl

Clinical Research Coordinator (part-time)

Clinical Research Coordinator

Research Lead

Licensed Clinical Social Worker - Temp

Clinical Exercise Physiologist

HL7 Data Analyst

Special Agent: Healthcare Services/Medical Background

Head of Clinical Operations (Oncology)

MedTech Part Time Clinical Consultant – San Francisco, CA

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