Top 15 Clinical research coordinator Jobs in Cape Coral Fl

Clinical Research Coordinator
Solaris Health Holdings LLC —Naples, FL
- Full-time
- Nursing
- BLS Certification
- HIPAA
Quick Apply
6d
Clinical Research Coordinator - Oncology
Lee Health —Fort Myers, FL
- $21.54 - $26.93 an hour
- Full-time
- Customer service
- Computer literacy
- Mid-level
6d
Hospice Clinical Care Coordinator
Affinity Care of Sarasota —Charlotte County, FL
- Full-time
- Mid-level
- Office
- High school diploma or GED
Quick Apply
Clinical Quality Coordinator-Hybrid-Fort Myers Market
Optum —Fort Myers, FL
- $20 - $36 an hour
- Full-time
- Current TB test
- Medical office experience
- Pass drug screening
Quick Apply
5d
Research Pharmacy Coordinator II
Florida Cancer Specialists & Research Institute —Fort Myers, FL
- Weekends as needed
- Background check
- Mid-level
- Office
- Tuition reimbursement
- 401(k) matching
10d
Clinical Ops Medical Records Coordinator
Radiology Regional Center, P.A —Fort Myers, FL
- $16 - $19 an hour
- 8 hour shift
- HIPAA
- Mid-level
- High school diploma or GED
13d
Clinical Coordinator
Physicians' Primary Care of Southwest Florida —Fort Myers, FL
- Monday to Friday
- CPR Certification
- Nursing
- BLS Certification
- Paid holidays
- Disability insurance
Quick Apply
RN Clinical Coordinator Alico FSED
HCA Florida Lehigh Hospital —Lehigh Acres, FL
- Full-time
- Mid-level
- Communication skills
- Employee stock purchase plan
- Disability insurance
Quick Apply
10d
RN Clinical Coordinator Alico FSED
HCA Florida Lehigh Hospital —Lehigh Acres, FL
- Full-time
- Mid-level
- Communication skills
- Employee stock purchase plan
- Disability insurance
Quick Apply
RN Clinical Coordinator Med Surg
HCA Florida Lehigh Hospital —Lehigh Acres, FL
- Full-time
- Mid-level
- Medical-Surgical
- Communication skills
- Employee stock purchase plan
- Disability insurance
Quick Apply
Licensed Clinical Coordinator Home Health
Empath Home Health —Naples, FL
- Mid-level
- Office
- Business development experience
- Continuing education credits
- Health insurance
Clinical Donation Coordinator I - PeeDee Region
WE ARE SHARING HOPE SC —United States
- On call
- Mid-level
- Operating room
- 2 years

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Clinical Research Coordinator - Oncology
Lee Health —Fort Myers, FL
Protocol Administration encompasses maintaining protocol compliance with cooperative groups and adhering to the LMHS IRC guidelines.
$21.54 - $26.93 an hour
6d
Hybrid Quality Assurance Specialist 2, Research Administration, FT,9A-5:30P
Baptist Health South Florida —Florida
The individual will be responsible for providing education and support to Operations staff in the implementation of, and adherence to, processes and workflows,…
$60,036.16 - $78,047.01 a year

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Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects’ rights through institutional IRB, federal and state regulations; answers…

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Clinical Research Coordinator

Solaris Health Holdings LLC -
Naples, FL

Quick Apply

Job Details

Full-time
6 days ago

Qualifications

BLS Certification
High school diploma or GED

Full Job Description

Description:

GENERAL SUMMARY

Clinical Research Coordinator works under Clinical Research Managers and are tasked with administering clinical trials. Responsibilities include managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.

Requirements:

ESSENTIAL JOB FUNCTION/COMPETENCIES

The responsibilities and duties described in this job description are intended to provide a general overview of the position. Duties may vary depending on the specific needs of the affiliate or location you are working at and/or state requirements. Responsibilities include but are not limited to:

Provide subject care and data collection procedures in adherence with the assigned study protocol and in accordance with good clinical research principals.
Review subject charts, database records, and other sources to screen and identify potential subjects for inclusion in study based on criteria described in the protocol.
Coordination and management of the clinical trial, communication with sponsor and authorities, visit coordination, sampling, time management and product accountability.
Data collection and management, collection and development of source documents, use of CRFs, managing patient registration, AEs, filing and archiving, managing monitoring visits, dealing with queries.
Maintain accurate records of the receipt, inventory, and dispensation of study drug and obtain and coordinate subject blood samples, cultures, tissues, and other specimens for laboratory analysis as described in study protocol.
Patient visits, data collection and transcription/EDC, prepare for monitor visits, protocol adherence to include height, weight, blood pressure, respirations, pulse temperature, O2 saturation.
Schedule appointments and organize materials to be used during study visits and ensure that all required tests are completed for each study visit per protocol.
Includes initial study start-up information/ requirements, dissemination of updated Investigator’s Brochures, protocols and informed consent information, online training initiated by sponsor, review of correspondence throughout study.
Completes Source Documentation-which includes completing and uploading all necessary documents to CRIO and maintaining all charts properly.
Medical Assessment-includes obtaining information from patient or chart regarding name of medication, start and stop dates, dose, and indication.
Biological Sampling Collection/Packaging/Shipping – includes serum and/or tissue collection, processing, packaging and shipping per study specific requirements.
Case Report Form (CRF) Entries and Management – includes data entry, query resolution in paper and/or electronic CRFs.
Investigational Product (IP) Management – includes receiving IP supplies, IP accountability, monitoring of temperature controls, destructions or return of IP.
Develop and/or Maintain Essential Documents – includes study specific training documents, study specific logs, patient questionnaires, patient pill diaries, lab requisition forms, other study specific forms.
Supply Chain Maintenance-Supplies Inventoried, stocking, organizing, and resupply order placed as required. Completed in Envi system.
Study Coordination- rooming, administer questionnaires, scheduling scans, set up room for procedures and wipe and clean equipment after procedures and visits.
Obtain/Maintain all required training- GCP, IATA,CPR Occasionally help the study coordinators at other offices such as the surgery center.
Performs other position related duties as assigned.
Employees shall adhere to high standards of ethical conduct and will comply with and assist in complying with all applicable laws and regulations. This will include and not be limited to following the Solaris Health Code of Conduct and all Solaris Health and Affiliated Practice policies and procedures; maintaining the confidentiality of patients' protected health information in compliance with the Health Insurance Portability and Accountability Act (HIPAA); immediately reporting any suspected concerns and/or violations to a supervisor and/or the Compliance Department; and the timely completion the Annual Compliance Training.

CERTIFICATIONS, LICENSURES OR REGISTRY REQUIREMENTS

BLS certification required, ACLS preferred.
License and certification as required by state.
RN, or LPN or MA preferred

KNOWLEDGE | SKILLS | ABILITIES

Knowledge of medical terminology, healthcare coding systems, and clinics functions.
Must be able to function in a team-oriented environment, display strong analytical, investigative, interpersonal and organizational skills, pay high attention to detail with consistent follow-through and be able to productively manage high volumes of work.
Knowledge of database management.
Maintain a working knowledge of all assigned study protocols and amendments.
Excellent verbal and written communication skills.
Skill in using computer programs and applications including Microsoft Office.
Delivers exceptional patient service throughout all interactions.
Excellent organizational skills and attention to detail.
Strong analytical and problem-solving skills.
Complies with all health and safety policies of the organization.
Complies with HIPAA regulations for patient confidentiality.
Ability to work independently and manage deadlines.
Ability to establish and maintain effective working relationships with patients, colleagues, physicians and the public; successfully manages interactions with challenging or difficult people.
Ability to deal compassionately, professionally, and courteously with patients, their families, physicians, and staff.
Ability to build relationships with patients and display empathy and compassion to patients.

EDUCATION REQUIREMENTS

High School Diploma or equivalent required.
Bachelor’s degree in a related field (biology, psychology, nursing or healthcare) preferred.

EXPERIENCE REQUIREMENTS

Experience with EPIC software preferred but not essential.
1-3 years of related experience preferred.

REQUIRED TRAVEL

Minimal travel required.

PHYSICAL DEMANDS

Carrying Weight Frequency

1-25 lbs. Frequent from 34% to 66%

26-50 lbs. Occasionally from 2% to 33%

Pushing/Pulling Frequency

1-25 lbs. Seldom, up to 2%

100 + lbs. Seldom, up to 2%

Lifting - Height, Weight Frequency

Floor to Chest, 1 -25 lbs. Occasional: from 2% to 33%

Floor to Chest, 26-50 lbs. Seldom: up to 2%

Floor to Waist, 1-25 lbs. Occasional: from 2% to 33%

Floor to Waist, 26-50 lbs. Seldom: up to 2%

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Refine Your Search

clinical research coordinator jobs in cape coral fl

Clinical Research Coordinator

Clinical Research Coordinator - Oncology

Hospice Clinical Care Coordinator

Clinical Quality Coordinator-Hybrid-Fort Myers Market

Research Pharmacy Coordinator II

Clinical Ops Medical Records Coordinator

Clinical Coordinator

RN Clinical Coordinator Alico FSED

RN Clinical Coordinator Alico FSED

RN Clinical Coordinator Med Surg

Licensed Clinical Coordinator Home Health

Clinical Donation Coordinator I - PeeDee Region

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