Top 65 Research coordinator Jobs in Miami Fl

Senior Clinical Research Coordinator
Indago Research & Health Center, Inc —Miami Lakes, FL
- $30 - $35 an hour
- Weekends as needed
- Background check
- Spanish
- HIPAA
- Paid holidays
- Disability insurance
Quick Apply
12d
Clinical Research Coordinator
Next Phase Research —Hollywood, FL
- From $65,000 a year
- Full-time
- Background check
- Spanish
- HIPAA
- Health insurance
- Dental insurance
Quick Apply
12d
Clinical Research Coord 3, MCVI Research, FT,8A-4:30P
Baptist Health South Florida —Miami, FL
- $32.12 - $41.76 an hour
- Full-time
- Computer literacy
- BLS Certification
- Mid-level
- Wellness program
- Health insurance
Supervisor Clinical Research Coordinator, Clinical Trials, FT,8:00A - 4:30P
Baptist Health South Florida —Miami, FL
- $83,400.24 - $108,420.31 a year
- Full-time
- Spanish
- Management
- Computer literacy
- Wellness program
- Health insurance
Clinical Research Coordinator, Clinical Trials, FT,8:00A - 4:30P
Baptist Health South Florida —Miami, FL
- $26.13 - $33.97 an hour
- Full-time
- Computer literacy
- BLS Certification
- No experience needed
- Wellness program
- Health insurance
Sr Clinical Research Coordinator
CAREERXCHANGE —Miami, FL
- $32 - $43 an hour
- Contract
- CPR Certification
- Mid-level
- 3 years
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
Clinical Research Coordinator I
DM CLINICAL RESEARCH GROUP —Doral, FL
- Writing skills
- High school diploma or GED
- Bachelor's degree
Clinical Research Coordinator
Hi Tech and Global Research —Coral Gables, FL
- $22 - $28 an hour
- Full-time
- Background check
- Spanish
- Blood sampling
- Paid time off
Quick Apply
4d
Clinical Research Coordinator, Clinical Trials
Baptist Health Herbert Wertheim Cancer Institute —Miami, FL
- $26.13 - $33.97 an hour
- Computer literacy
- BLS Certification
- No experience needed
- Wellness program
- Health insurance
Clinical Research Coordinator
DermCare Management —Hollywood, FL
- $28 - $32 an hour
- Spanish
- OSHA
- Patient monitoring
- Paid holidays
- Health insurance
Quick Apply
PER DIEM CLINICAL RESEARCH COORDINATOR
SRA Trials —Doral, FL
- $30 an hour
- Per diem
- Spanish
- English
- Mid-level
Quick Apply
13d
Clinical Research Coordinator 1 (A) Full Time Bascom Palmer Eye Institute Miami, FL
University of Miami —Miami, FL
- Full-time
- Bachelor's degree
- 1 year
- Communication skills
- Health insurance
- Dental insurance
Research Coordinator
Hope Clinical Trials —Coral Gables, FL
- $20 - $25 an hour
- Full-time
- Patient monitoring
- HIPAA
- Data entry
Quick Apply
5d
Clinical Research Coordinator - Per Diem
University of Miami —Miami, FL
- Part-time
- Mid-level
- 3 years
- Databases
- Health insurance
- Dental insurance
6d
Clinical Research Coordinator
SRA Trials —Miami, FL
- $57,000 - $80,000 a year
- 8 hour shift
- Spanish
- Vital signs
- English
- Health savings account
- Health insurance
Quick Apply
Clinical Research Coordinator 1 Full Time Bascom Palmer Eye Institute Miami, FL
University of Miami —Miami, FL
- Weekends as needed
- Bachelor's degree
- Experience equivalent to degree accepted
- 1 year
- Health insurance
- Dental insurance
Clinical Research Coordinator 1
University of Miami —Miami, FL
- Weekends as needed
- Psychiatry
- University
- Bachelor's degree
- Health insurance
- Dental insurance
DRAA Research Department Coordinator
Larkin Community Hospital —South Miami, FL
- Full-time
- Word processing
- Mid-level
- Office
Clinical Research Coordinator 2 Full Time Bascom Palmer Eye Institute Miami, FL
University of Miami —Miami, FL
- Weekends as needed
- Mid-level
- Bachelor's degree
- Experience equivalent to degree accepted
- Health insurance
- Dental insurance

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Senior Clinical Research Coordinator

Indago Research & Health Center, Inc -
Miami Lakes, FL

Quick Apply

Job Details

Full-time
$30 - $35 an hour
12 days ago

Benefits

Paid holidays
Disability insurance
Relocation assistance
Health insurance
Dental insurance
401(k)
Tuition reimbursement
Military leave
Paid time off
Employee assistance program
Vision insurance
401(k) matching
Professional development assistance
Bereavement leave
Life insurance
Referral program

Qualifications

Spanish
CCRC
Clinical research
HIPAA
English
Attention to detail
Patient interaction
Training & development
Medical terminology

Full Job Description

Job highlights:
The Clinical Research Coordinator III is responsible for the overall coordination, organization, management, and efficient implementation of clinical trials. The CRC will complete all study-related procedures and distribute study medications and instructions to research subjects under the direction of the Investigators, Site staff, CROs, and Sponsors. They will maintain accurate confidential files and documentation of the study participants. The CRC will also engage in the explanation of what is expected of the research subjects and understand their concerns, requiring excellent interpersonal and communication skills. All duties are carried out in accordance with the company policies, SOPs, and Good Clinical Practice (GCP) as well as all applicable Local, State, and Federal regulations..

Job functions:

Review study protocols and complete study training.
Ensures the team receives access, approvals, and study supplies before study initiation.
Attends I.M., S.I.V., and any other training session required by the Sponsor.
Develop their source documents following the Site’s templates and give them to their direct supervisor for approval.
Meets with the Regulatory Department to ensure that the study is captured correctly in the system, including the window period between study visits, and verifies the patient stipend reflects the same amount as in the ICF.
Reviews of the weekly report prepared by the Team Lead CRC during the weekly meetings
Attend meetings to discuss the week’s progress, performance, and the upcoming studies.
Meets with the Laboratory personnel, Assistant Coordinator, and Recruitment Department before the study's initiation to train them on the protocol.
Ensures study staff is aware and has been trained in the latest protocol amendment.
Conduct thorough reviews of electronic and paper diaries with study participants, either in person or via phone, to ensure accuracy, compliance, and completeness of recorded information.
Ensures that all personnel listed on the Delegation Log have completed all the training required by Sponsors and have obtained access to vendor portals.
Reviews and maintains each tab of the Regulatory Binder.
Consents study participants following the Site’s SOPs.
If data entry personnel are not available, the CRC must enter the subject’s data in EDC within 24 hours of the visit being performed.
Keep the Site’s internal system updated regarding the subject status in the trial.
Ensures all deviations, violations, AEs, and SAEs are captured, recorded, followed, and reported to Sponsor/IRB in a timely manner.
Performs study-related procedures in compliance with protocols and the Site’s SOPs.
Target enrollment goals and maintain a close line of communication with the study subjects to keep them engaged in the trial while trying to achieve a higher retention rate.
Ensures that the Laboratory is following protocol requirements and that all samples are successfully packed and sent to the Central/Local Laboratory, as indicated.
Ensures proper follow-up through telephone contacts or certified letters when subject and emergency contact are not responding, continuing following up with subjects that have missed their appointments until they come back for their visit or are declared LTFU.
Confirm with the Front desk personnel, Laboratory technicians, and Assistant CRC, subjects scheduled for the following day.
Assists Clinical Research Associates or Auditors during on-site or remote monitoring visits, answering any queries generated and resolving pending action items within 7 days of the monitoring visit.
Maintains PI/Sub-I/Lead CRC and is always informed on all aspects of the trial.
Completes additional tasks as required by a specific protocol.

Desired qualifications:

Works well in a team environment.
Certified Clinical Research Coordinator preferred.
Strong knowledge of the clinical research process, including Regulatory requirements, Good Clinical Practices (GCP), HIPAA, and International Conference of Harmonization (ICH) guidelines.
Strong independent research ability.
Strong attention to detail and accuracy in documentation.
Ability to work effectively with diverse patient populations.
Prior experience in monitoring and managing adverse events.
General knowledge of clinical research preferred.
Clinical Terminology proficiency.
Excellent written and verbal communication skills.
High attention to detail and organization.
Ability to multitask.
Bi-lingual English/Spanish required.
Ability to work after hours and weekends if needed.
Knowledge of Microsoft Office 365.

Job Type: Full-time In-person, Monday to Friday – 8:00 am – 4:30 pm

Benefits:

Medical, Dental, and Vision Insurance
Life Insurance (includes Will Preparation, Employee Assistance Program (EAP), and Travel Assistance)
Short & Long-Term Disability
Workers’ Compensation Insurance
COBRA Continuation Coverage
401(k) Retirement Savings Plan with employer match
Paid Time Off (PTO)
Paid Holidays
Bereavement Leave
Family and Medical Leave Act (FMLA)
Military Leave
Referral Program
Tuition Assistance/Professional Development
Certification Reimbursement

Indago Research & Health Center, Inc., is firmly committed to Equal Employment Opportunity (EEO) and prohibits employment discrimination for employees and applicants based on age, race, color, pregnancy, gender, gender identity, sexual orientation, national origin, religion, marital status, citizenship, disability or protected veteran or other status protected by Federal, State, and/or Local law.

Job Type: Full-time

Pay: $30.00 - $35.00 per hour

Benefits:

401(k)
401(k) matching
Health insurance
Life insurance
Paid time off
Professional development assistance
Referral program
Relocation assistance
Tuition reimbursement

Experience:

Clinical research: 5 years (Required)

License/Certification:

CCRC (Preferred)

Work Location: In person

Quick Apply

Refine Your Search

research coordinator jobs in miami fl

Senior Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coord 3, MCVI Research, FT,8A-4:30P

Supervisor Clinical Research Coordinator, Clinical Trials, FT,8:00A - 4:30P

Clinical Research Coordinator, Clinical Trials, FT,8:00A - 4:30P

Sr Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator I

Clinical Research Coordinator

Clinical Research Coordinator, Clinical Trials

Clinical Research Coordinator

PER DIEM CLINICAL RESEARCH COORDINATOR

Clinical Research Coordinator 1 (A) Full Time Bascom Palmer Eye Institute Miami, FL

Research Coordinator

Clinical Research Coordinator - Per Diem

Clinical Research Coordinator

Clinical Research Coordinator 1 Full Time Bascom Palmer Eye Institute Miami, FL

Clinical Research Coordinator 1

DRAA Research Department Coordinator

Clinical Research Coordinator 2 Full Time Bascom Palmer Eye Institute Miami, FL

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