Top 70 Clinical research coordinator Jobs in Largo Fl

CLINICAL RESEARCH COORDINATOR I
Moffitt Cancer Center —Tampa, FL
- Full-time
- Hybrid work
- Psychology
- Business Administration
- Social Work
- Paid training
- Relocation assistance
Clinical Research Coord I
Orlando Health —Tampa, FL
- Full-time
- Nursing
- BLS Certification
- Clinic
- Paid parental leave
- Health insurance
Clinical Research Coord I
Bayfront Health —Tampa, FL
- Full-time
- Nursing
- BLS Certification
- Clinic
- Paid parental leave
- Health insurance
Clinical Research Coordinator
Alcanza Clinical Research —Largo, FL
- Full-time
- Spanish
- LVN
- HIPAA
- Health savings account
- Disability insurance
Quick Apply
Clinical Research Coordinator, Level 2
Shriners Hospitals for Children —Tampa, FL
- $55,286.40 - $82,908.80 a year
- Full-time
- 18 years or older
- Hospital
- HIPAA
Quick Apply
CLINICAL TRIALS SCREENING COORDINATOR I
Moffitt Cancer Center —Tampa, FL
- Full-time
- Hybrid work
- Clinic
- 2 years
- Entry level
- Paid training
- Relocation assistance
Clinical Research Coordinator
BayCare —Tampa, FL
- PRN
- 5 years
- HIPAA
- Mid-level
- Health insurance
- Dental insurance
6d
Clinical Research Coord I
Florida Medical Clinic —Tampa, FL
- Full-time
- Nursing
- BLS Certification
- Clinic
- Paid parental leave
- Health insurance
Clinical Research Coordinator
ALLIANCE CLINICAL LLC —Palm Harbor, FL
- Full-time
- Patient monitoring
- Customer service
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Clinical Administrative Coordinator
UnitedHealthcare —Tampa, FL
- $18 - $32 an hour
- 8 hour shift
- Remote
- 18 years or older
- Microsoft Outlook
- Pass drug screening
- AD&D insurance
- Employee stock purchase plan
14d
Clinical Research Coordinator II
Johns Hopkins All Children's Hospital —Saint Petersburg, FL
- Full-time
- Nursing
- Mid-level
- Bachelor's degree
Clinical Research Infusion Rn I
Moffitt Cancer Center —Tampa, FL
- $35.05 - $52.56 an hour
- Full-time
- Nursing
- Patient monitoring
- RN License
9h
Clinical Research Coordinator
NMC Research —Tampa, FL
- $18 - $35 an hour
- Urgently hiring
- Spanish
- Nursing
- HIPAA
- Paid time off
- Employee discount
Quick Apply
Clinical Quality Coordinator RN
AdventHealth Tampa —Tampa, FL
- $72,786.83 - $135,385.27 a year
- Full-time
- Microsoft Word
- Background check
- Nursing
- Paid parental leave
- Disability insurance
6d
Clinical Research Coordinator
United Digestive —Tampa, FL
- Full-time
- BLS Certification
- Pass drug screening
- HIPAA
Quick Apply
Clinical Coordinator
BrightStar Care Pinellas —Largo, FL
- $30 - $35 an hour
- Full-time
- Background check
- Nursing
- Microsoft Excel
- Health insurance
- Paid time off
Quick Apply
2d
CLINICAL RESEARCH RN II
Moffitt Cancer Center —Tampa, FL
- Full-time
- Nursing
- Patient monitoring
- RN License
RESEARCH SAMPLING COORDINATOR I
Moffitt Cancer Center —Tampa, FL
- Full-time
- Hospital
- No experience needed
- High school diploma or GED
- Dental insurance
- Paid time off
Clinical Coordinator - Bayfront Hospital
Orlando Health —Saint Petersburg, FL
- Full-time
- Nursing
- Management
- RN License
EPIC RESEARCH TOOLS CLINICAL APPLICATIONS ANALYST II
Moffitt Cancer Center —Tampa, FL
- $87,092.20 - $132,717.00 a year
- Full-time
- Remote
- System design
- Mid-level
- 3 years

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CLINICAL RESEARCH COORDINATOR I

Moffitt Cancer Center -
Tampa, FL

Apply Now

Job Details

Full-time

Benefits

Paid training
Relocation assistance
Paid orientation

Qualifications

CCRC
Adverse event reporting
Clinical incident reports
Care documentation
Sociology
Social Sciences
Research project coordination
Compliance monitoring
Public Health
Psychology
Clinical trial patient safety management
Implementing research protocols
Patient recruitment
CCRP
Business Administration
Patient interaction
Social Work
Patient education
Business
Care coordination
Associate's degree
Entry level

Full Job Description

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.

As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces.

Summary

Are you looking for an opportunity to impact lives and be a central part of a dynamic and innovative team in the fight against cancer? As a Moffitt Clinical Research Coordinator, you’ll bring hope to patients by delivering tomorrow’s cancer treatments today! You will have the opportunity to interact directly with patients, enroll, educate and guide them through the experiences of taking part in clinical trials while receiving innovative treatments as part of a therapeutic clinical trial. You will be the member of the Team that ensures the trial is moving forward safely, smoothly, and according to plan. Our Clinical Research Coordinators come from a variety of backgrounds and experiences, including social sciences (public health, social work, sociology, psychology, communications, and more), biological sciences, business, and humanities. The Clinical Research Coordinator role is a terrific opportunity for those who have already worked in other areas of healthcare as well as those who are looking for a new and exciting way to contribute through their career. This position offers a Monday through Friday schedule and hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period. Moffitt offers paid training and orientation through its CTO (Clinical Trails Office) Academy. Position tiers may vary according to experience. Relocation assistance may be provided. https://moffitt.org/clinical-trials-research/clinical-trials/clinical-trials-administration/ These positions work closely with patients, patient families, study sponsors (from smaller pioneer biotech companies through large pharmaceutical companies), and the Clinical Trial Team that includes physicians, pharmacists, nurses, data monitors and data managers. Position Highlights: • Coordinate patient care by collaborating with medical staff and document in accordance with standards and regulatory guidelines with direction of a mentor or supervisor. • Act as liaison between the investigators, Moffitt regulatory staff and the sponsor. • Will assist to screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. • Responsible for data and source documentation and adverse experience reporting. • Perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study protocol. • Will work under general supervision and direction from the supervisor and Principal Investigator to implement and coordinate research, including administrative procedures. Credentials and Qualifications: • *Bachelor’s degree (preferred field of study scientific, health related or business administration program) with one (1) year of relevant clinical, health related, scientific, business or research experience *In lieu of bachelor’s degree, Associate’s degree with 2 years of relevant clinical, health related, scientific, business or research experience* • CCRP/CCRC or equivalent preferred.

Salary Range

Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.

We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.

Moffitt Career Site

If you have the vision, passion, and dedication to contribute to our mission,

then we have a place for you!

1. Equal Employment Opportunity

Moffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence.

2. Reasonable Accommodation

Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. Moffitt endeavors to make moffitt.org/careers accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact one of the Human Resources receptionists by phone at 813-745-7899 or by email at [email protected]. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.

Read more information about your EEO rights under the law.

Transparency in Coverage Rule

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Refine Your Search

clinical research coordinator jobs in largo fl

CLINICAL RESEARCH COORDINATOR I

Clinical Research Coord I

Clinical Research Coord I

Clinical Research Coordinator

Clinical Research Coordinator, Level 2

CLINICAL TRIALS SCREENING COORDINATOR I

Clinical Research Coordinator

Clinical Research Coord I

Clinical Research Coordinator

Clinical Administrative Coordinator

Clinical Research Coordinator II

Clinical Research Infusion Rn I

Clinical Research Coordinator

Clinical Quality Coordinator RN

Clinical Research Coordinator

Clinical Coordinator

CLINICAL RESEARCH RN II

RESEARCH SAMPLING COORDINATOR I

Clinical Coordinator - Bayfront Hospital

EPIC RESEARCH TOOLS CLINICAL APPLICATIONS ANALYST II

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Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.

If you have the vision, passion, and dedication to contribute to our mission,

then we have a place for you!

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